Accuvix A30 SVM V3.0 Rev2 Eng

A30 Service Manual
KOREA
Document No. CSD-SMEA30
Version 3.0
H/W Compatibility
Board A30 V2.0 A30 V3.0 Compatibility
BP 0A 1A ｘ
BE 0B x -
PCC x 0A -
BF 1A 1A Ｏ
AC 1A 1A Ｏ
CW 0A 0B ｘ
REAR 1A x -
REAR L x 0A ｘ
REAR R x 0A ｘ
CP 0B 1A ｘ
DVI 2B x -
PCIE 0A x -
Body
MI97-01090A MI97-01090B ｘ
Frame
Recovery S/W Compatibility

CD A30 V2.0 A30 V3.0 Compatibility
#1 CD 2.00 3.00 ｘ
#2 CD 2.00 3.00 ｘ
Copyright©2012 by Samsung Medison

Safety Standards
Classifications:
▶ Type of protection against electrical shock: Class I

▶ Degree of protection against electrical shock (Patient connection): Type BF equipment
▶Degree of protection against harmful ingress of water: Ordinary equipment
▶Degree of safety of application in the presence of a flammable anesthetic material with air
or with oxygen or nitrous oxide: Equipment not suitable for use in the presence of a
flammable anesthetic mixture with air or with oxygen or nitrous oxide.
▶Mode of operation: Continuous operation
Electromechanical safety standards met:
▶Medical Electrical Equipment, Part 1: General Requirements for Basic Safety and Essential
Performance [IEC 60601-1:2005]
▶Medical Electrical Equipment, Part 1-2: General Requirements for Basic Safety and
Essential
Performance - Collateral Standard: Electromagnetic Compatibility - Requirements and
Tests [IEC 60601-1-2:2007]
▶ Medical Electrical Equipment, Part 1-6: General Requirements for Basic Safety and
Essential
Performance- Collateral Standard: Usability [IEC 60601-1-6:2006]
▶ Medical Electrical Equipment, Part 2-37: Particular Requirements for the Basic Safety and
Essential
Performance of Ultrasonic Medical Diagnostic and Monitoring Equipment [IEC60601-2-
37:2007]
▶ Medical Electrical Equipment, Part 1: General Requirements for Safety
[IEC 60601-1:1988 with A1:1991 and A2:1995]
▶ Medical Electrical Equipment, Part 1: General Requirements for Safety – 1 Collateral
Standard: safety
Requirement for Medical Electrical Systems [IEC 60601-1-1:2000]
▶ Medical Electrical Equipment, Part 1: General Requirements for Safety - 2 Collateral
Standard:
Electromagnetic Compatibility - Requirements and Test
[IEC 60601-1-2:2001, A1:2004]
▶Medical Electrical Equipment, Part 1: General Requirements for Safety - 4 Collateral
Standard:
Programmable Electrical Medical Systems [IEC 60601-1-4: 1996, A1:1999]
▶ Medical Electrical Equipment, Part 2: Particular Requirements for Safety - 37
Ultrasonic Medical
Diagnostic and Monitoring Equipment [IEC60601-2-37: 2001 with A1:2004, A2:2005]
▶ Medical Devices – Application of Risk Management to Medical Devices [ISO 14971:2007]
▶ Medical Electrical Equipment, Part 1: General Requirements for Safety[UL60601-1:2003]
▶ Medical Electrical Equipment - Part 1: General Requirements for Safety[CAN/CSA 22.2]
No.601.1-M90:1990, with R2003, with R2005]
▶ Biological Evaluation of Medical Devices [ISO10993 : 2009]
▶ Standard Means for the Reporting of the Acoustic Output of Medical Diagnostic
Ultrasonic Equipment [IEC61157:2007]
Declarations:
This is CSA symbol for Canada and United States of America
This is manufacturer’s declaration of product compliance

with applicable EEC directive(s) and the European notified
0123 body.
This is manufacturer’s declaration of product compliance

with applicable EEC directive(s).
This is GMP symbol for Good Manufacturing Practice of

Korea quality system regulation.
Certificate of Excellent Service Quality is to certify that the

above company has served customers with excellent
services by the Ministry of Knowledge Economy Republic
of Korea.
Precautions
Read the manual before repairing the product and learn the repair method and precautions
fully.
If not fulfilling precautions, safety accidents may happen to service engineers and product
users, patients due to electrical shock (machines or other risks).
1. Refer to the service manual when repairing the product.

2. In particular, read instructions for use of ‘Chapter 2 safety’.
3. This product is the equipment for diagnostic imaging so do not use it for any other
purpose other than diagnostic imaging.
4. Only Medison Service team and authorized engineers can repair this product.
5. An unqualified person should not repair this product and Medison Co., Ltd. does not take
responsibility for caused problems.
6. Medison Co., Ltd. does not take responsibility for the problem of equipment caused
by negligent behavior or careless management of a user.
7. The following terms are used to emphasize the details to which special attention should
be paid.
˙A
D ˙N
˙G˙ E˙ R
˙
 This is information on emergency situations and risks such as death or serious injury that
may occur when you ignore the instructions.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
 This is warning to prevent damage of property or serious accidents.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
 This is caution to prevent minor accidents and property damage.
˙O
N ˙ T˙ Ė
E˙
 This is information for users such as installation requiring attention, operation or

maintenance, storage etc., though not directly related to risk situation.
Service Manual
Contents
Chapter 1 About product

1.1 Overview ............................................................................................................................ 1-1
1.2 Main functions of A30 ...................................................................................................... 1-2
1.3 Product configuration ........................................................................................................ 1-3
1.3.1 Body ..................................................................................................................... 1-3
1.3.2 LCD monitor ........................................................................................................ 1-4
1.3.3 Control panel ....................................................................................................... 1-5
1.3.4 Probe ................................................................................................................... 1-5
1.4 Product specification ........................................................................................................ 1-6
Chapter 2 Safety
2.1 Overview ............................................................................................................................ 2-1
2.2 Safety matters ................................................................................................................... 2-2
2.2.1 Safety symbols ................................................................................................... 2-2
2.2.2 Location of labels ................................................................................................ 2-4
2.3 Electrical Safety ................................................................................................................ 2-7
2.3.1 Prevention of electrical shock............................................................................ 2-7
2.3.2 ECG related matters .......................................................................................... 2-8
2.3.3 ESD ...................................................................................................................... 2-8
2.3.4 EMI ....................................................................................................................... 2-9
2.3.5 EMC ..................................................................................................................... 2-9
2.4 Mechanical safety ...........................................................................................................2-15
2.4.1 Precautions for moving ....................................................................................2-15
2.4.2 Precautions for use ..........................................................................................2-16
2.4.3 Precautions while using monitor .....................................................................2-16
2.5 Biological Safety .............................................................................................................2-18
2.5.1 ALARA principle................................................................................................2-18
2.6 Protection of the environment ........................................................................................2-30
Contents
Chapter 3 Product installation
3.1 Overview ............................................................................................................................ 3-1
3.2 Transportation ................................................................................................................... 3-3
3.2.1 Precautions for transportation .......................................................................... 3-3
3.2.2 Humidity and temperature ................................................................................ 3-3
3.2.3 How to transport ................................................................................................ 3-3
3.3 Unpacking.......................................................................................................................... 3-4
3.3.1 Dismantling of the product box ........................................................................ 3-4
3.3.2 Checking product components ........................................................................ 3-5
3.4 Installation conditions. ...................................................................................................... 3-6
3.4.1 Precautions ........................................................................................................ 3-6
3.4.2 Installation place ................................................................................................ 3-6
3.5 How to Install ..................................................................................................................... 3-7
3.5.1 Installation Safety .............................................................................................. 3-7
3.5.2 Connecting power cable ................................................................................. 3-8
3.5.3 Connecting network cable ................................................................................ 3-9
3.5.4 Connecting Foot switch .................................................................................... 3-9
3.5.5 Connecting probe ............................................................................................3-10
3.6 Turning on the product ...................................................................................................3-11
3.7 Shutting down Product .................................................................................................3-12
3.7.1 Power switch ....................................................................................................3-12
3.7.2 Power circuit breaker ......................................................................................3-12
3.8 Connecting peripherals ..................................................................................................3-13
3.8.1 Internal peripherals..........................................................................................3-13
3.8.2 External peripherals ........................................................................................3-13
3.9 Setup ..............................................................................................................................3-15
3.10 System General Setup...................................................................................................3-16
3.11 Screen Setup (Display) ..................................................................................................3-19
3.12 Annotate ..........................................................................................................................3-22
3.13 Peripherals Setup .........................................................................................................3-27
3.14 User Defined Key ...........................................................................................................3-30
3.15 Miscellaneous .................................................................................................................3-31
3.16 Option Setup (Option) ....................................................................................................3-35
Contents
Service Manual
3.17 DICOM Setup (option) ...................................................................................................3-36

3.18 Auto Calc .........................................................................................................................3-47
3.19 System information.........................................................................................................3-48
3.20 Utility .................................................................................................................................3-49
Chapter 4 Product inspection

4.1 Overview ............................................................................................................................ 4-1
4.2 Turning on the product ................................................................................................... 4-2
4.3 Monitor ............................................................................................................................... 4-3
4.3.1 Screen configuration ......................................................................................... 4-3
4.4 Control panel ..................................................................................................................... 4-5
4.4.1 Detailed functions of control panel .................................................................. 4-6
4.4.2 Keyboard ............................................................................................................ 4-8
4.4.3 Touch screen ................................................................................................... 4-8
4.4.4 Adjustment of control panel............................................................................4-10
4.5 Performance checking ...................................................................................................4-11
4.5.1 Basic checking .................................................................................................4-11
4.5.2 Detailed checking ............................................................................................4-12
Chapter 5 Product Structure

5.1 Overview .................................................................................................................................................................5-1
5.2 System Block Diagram ..................................................................................................................................5-3
5.3 Basic structure of ACCUVIX A30G ........................................................................................................5-4
5.3.1 Overview………………...............................................................................................................................5-4
5.3.2 Ultrasound System Part.....................................................................................................................5-4
5.3.3 PC Part…… 5-5
5.3.4 User Interface Part ................................................................................................................................5-5
5.3.5 AC to DC Power Module .................................................................................................................5-5
5.4 PSA…… 5-6
5.5 Beam former Board ........................................................................................................................................5-8
5.6 CW Board............................................................................................................................................................5-11
Contents
5.7 PC Carrier Board.............................................................................................................................................5-14
5.8 PC Module .........................................................................................................................................................5-22
5.12 Software DSC....................................................................................................................................................5-23
5.13 Rear Board ..........................................................................................................................................................5-25
5.14 Control Panel ....................................................................................................................................................5-27
5.15 Analog Control Board ................................................................................................................................5-30
5.16 Power Supply....................................................................................................................................................5-31
Chapter 6 Basic maintenance

6.1 Overview ............................................................................................................................ 6-1
6.2 System information........................................................................................................... 6-2
6.3 Windows Mode ................................................................................................................. 6-3
6.4 Version up ......................................................................................................................... 6-4
6.4.1 Software version up .......................................................................................... 6-4
6.4.2 Hardware version up ......................................................................................... 6-5
6.5 Admin Mode ...................................................................................................................... 6-6
6.5.1 Admin Mode Entry Method .............................................................................. 6-6
6.5.2 Function of Admin Mode .................................................................................. 6-6
6.6 Addition and deletion of Option .....................................................................................6-13
6.6.1 Kinds of Option ................................................................................................6-13
6.6.2 Registration of Option .....................................................................................6-13
6.6.3 Deletion of Option............................................................................................6-16
Chapter 7 Diagnosis of failure

7.1 Overview ............................................................................................................................ 7-1
7.2 Power ................................................................................................................................. 7-2
7.2.1 Cannot turn on power ....................................................................................... 7-2
7.2.2 Cannot turn off power ....................................................................................... 7-2
7.2.3 Turned off by itself ............................................................................................. 7-3
7.3 Monitor ............................................................................................................................... 7-4
7.3.1 Nothing on the screen....................................................................................... 7-4
7.3.2 Changed screen color....................................................................................... 7-4
Contents
Service Manual
7.4 Error message .................................................................................................................. 7-5

7.4.1 Product is stopped after an error while booting ............................................. 7-5
7.4.2 An error occurs but the product is operating .................................................. 7-5
7.4.3 Error code........................................................................................................... 7-5
7.5 Image ................................................................................................................................. 7-6
7.5.1 No BW Mode Image Echo ............................................................................... 7-6
7.5.2 No BW Mode Image Format .......................................................................... 7-6
7.5.3 Lining phenomenon like raining on BW Mode Image (Noise) ..................... 7-6
7.5.4 Bad PW Doppler Mode..................................................................................... 7-7
7.5.5 Bad CW Doppler Mode .................................................................................... 7-7
7.5.6 Bad Color Doppler Mode.................................................................................. 7-7
7.5.7 Bad Motion Mode .............................................................................................. 7-7
Chapter 8 Disassembly
8.1 Overview 8-1
8.2 Disassembly Front Low Part ........................................................................................................................8-4
8.2.1 Preparation ...........................................................................................................................................8-4
8.2.2 Front Low Cover..................................................................................................................................8-4
8.2.3 PSA ASSY .................................................................................................................................................8-4
8.2.4 Main Board (BF, BE, CW, MTR)..................................................................................................8-4
8.2.5 ECG Module ........................................................................................................................................8-5
8.3 Disassembly Rear Low Part Rear Low Part ..........................................................................................8-6
8.3.1 Preparation..............................................................................................................................................8-6
8.3.2 Rear Cover ASSY .................................................................................................................................8-6
8.3.3 HDD ...........................................................................................................................................................8-9
8.3.4 DC to DC Power Module ..........................................................................................................8-10
8.3.5 AC to DC Power Module ...........................................................................................................8-11
8.3.6 Body Top Cover ................................................................................................................................8-12
8.3.7 Rear Fan .................................................................................................................................................8-13
8.3.8 Rear Board ……………..…………………………………………………………………………..…8-14
8.4 Disassembly User Interface Part ............................................................................................................8-15
8.4.1 Preparation ........................................................................................................................................8-15
8.4.2 Control Panel ASSY ........................................................................................................................8-15
8.4.3 Touch Panel .........................................................................................................................................8-16
Contents
8.4.4 Track Ball............................................................................................................................................8-17
8.4.5 Control Panel Board ..................................................................................................................8-18
8.4.6 Alpha-Numeric Board ..............................................................................................................8-19
8.5 Disassembly Rear Upper Part .. .................................................................................................................8-20
8.5.1 Preparation ....................................................................................................................................8-20
8.5.2 Handle AY .........................................................................................................................................8-20
8.5.3 Body Arch Inner Right & Left Cover .............................................................................8-21
8.5.4 DVD.......................................................................................................................................................8-22
8.5.5 Speaker Right & Left ................................................................................................................8-24
8.6 Disassembly LCD & ARM ...........................................................................................................................8-24
8.6.1 Preparation .....................................................................................................................................8-24
8.6.2 LCD………. ............................................................................................................................................8-24
8.6.3 LCD ARM ...........................................................................................................................................8-25
8.7 Disassembly Side Cover & Body Arch Front ................................................................................8-26
8.8.1 Preparation .....................................................................................................................................8-26
8.8.2 Body Side Right & Left Cover ............................................................................................8-27
8.8.3 Body Arch Front Cover ............................................................................................................8-28
Chapter 9 Probe
9.1 Overview ............................................................................................................................ 9-1
9.2 Probe list ............................................................................................................................ 9-2
9.3 Temperature index table (TI Table) ................................................................................ 9-5
9.4 Use of ultrasound gel ...................................................................................................... 9-6
9.5 Probe safety matters ........................................................................................................ 9-7
9.6 Cleaning and disinfection of probe ................................................................................. 9-9
9.7 MPTEE Probe (option)...................................................................................................9-15
Chapter 10 Maintenance and management

10.1 Overview ..........................................................................................................................10-1
10.2 Product Management.....................................................................................................10-2
10.2.1 Product Installation and Storage ....................................................................10-2
10.2.2 Cleaning and disinfection ...............................................................................10-2
Contents
Service Manual
10.2.3 Air Filter management ....................................................................................10-4

10.2.4 Accuracy test ...................................................................................................10-5
10.3 Information Management...............................................................................................10-6
10.3.1 User Setting Back-up ......................................................................................10-6
10.3.2 Patient information Restore............................................................................10-6
10.3.3 Software ...........................................................................................................10-6
Chapter 11 Service Parts List

11.1 Overview ..........................................................................................................................11-1
11.2 Body Cover......................................................................................................................11-2
11.3 Ultrasound System Part ...............................................................................................11-4
11.4 LCD & ARM.....................................................................................................................11-5
11.5 PC Part ............................................................................................................................11-6
11.6 Power Part .......................................................................................................................11-8
11.7 User Interface Part..........................................................................................................11-9
11.8 ETC Part ....................................................................................................................... 11-10
11.9 Options.......................................................................................................................... 11-11
Contents
Chapter 1 Safety
Service Manual
Chapter 1 Safety
1.1 Overview
Chapter 2 describes important matters to repair ACCUVIX A30 safely. This is for
safety of additional equipment including ultrasound system, Probe, recording
device etc. Before installing or repairing the product, you must read and
understand all of the information provided here in. This product should be used by
doctors eligible to use Medical Device or people approved by doctors. If a health
care provider or ordinary person not eligible to use Medical Device uses three-
dimensional ultrasound (3D, 4D) for a pregnant woman for a long time to
take commemorative photographs of a fetus or record video, it may cause the
adverse effect to the fetus. In case of three-dimensional ultrasound
imaging diagnostic device, video recording etc. except for purposes of fetus
diagnosis may have a harmful effect on a fetus so please observe use purpose.
Contents
1.1 Overview .................................................................................................................. 1-1

1.2 Matters on safety ..................................................................................................... 1-2
1.2.1 Safety signs ............................................................................................... 1-2
1.2.2 Label........................................................................................................... 1-4
1.3 Electrical Safety ....................................................................................................... 1-7
1.3.1 Prevention of ........................................................................................... 1-7
1.3.2 ECG related matters................................................................................. 1-8
1.3.3 ESD ............................................................................................................ 1-8
1.3.4 EMI ............................................................................................................. 1-9
1.3.5 EMC ........................................................................................................... 1-9
1.4 Mechanical safety.................................................................................................. 1-15
1.4.1 Precautions for moving .......................................................................... 1-15
1.4.2 Precautions for use................................................................................. 1-16
1.4.3 Precautions while using monitor ........................................................... 1-16
1.5 Biological Safety .................................................................................................... 1-18
1.5.1 ALARA principle ...................................................................................... 1-18
1.6 Protection of the environment .............................................................................. 1-30
Chapter 1 Safety 1-1

1.2 Matters on safety
1.2.1 Safety symbols

International Electro technical Commission (IEC) established safety and guidance
symbols on medical electronic equipment. The established symbols are as follows.
Symbol Meaning
AC power supply
Warning on the danger of electrical shock
Classification according to the degree of protection on

electrical risk (Type BF)
Classification according to the degree of protection on

electrical risk (Type CF)
Power switch (Supplying/shutting off power to products)
OFF(Shutting off power supply to part of the product)
WARNING: This is the warning to prevent serious

accidents or damage to property.
CAUTION: This is the attention to prevent minor accidents

or damage to property.
See the service manual
ON (Supplying power to part of the product)
Equipotential terminal

Service Manual
Symbol Meaning
High-tension part greater than alternating 1000 V or direct

current 1500 V
Protective earth terminal
Data output port
Data input port
Data input and output port
Left and right audio / Video input port
Left and right audio / Video output port
Print remote output
Foot switch connector
ECG connector
USB connector
MIC connector
Flood proof type device
Drip proof type device
Probe connector

Symbol Meaning
ESD related warning sign
Do not sit on control panel.
No pushing
No leaning
Follow the service manual

Service Manual
1.2.2 Label
The phrases on ‘Warning’ or ‘Caution’ to protect the product are attached to the
product surface.
[Label 1. ID Label]
[Label 2. Caution attached to the bottom of OUTLET]
[Label 3. ‘TIP-OVER’ related attention]

[Label 4. Control panel related caution]
[Label 5. Probe ID Label]

Service Manual
1.3 Electrical Safety

This product is classified into Class I device of Type BF의 Class I.
1.3.1 Prevention of electrical shock

Dangerous current within hospitals can be caused by potential differences
between connecting device and touchable conductive part in the medical office. A
solution to this is the exact connection of equipotential terminal. Equipotential
terminal of the medical device should be connected to equipotential connecting
part of the medical office as shown in the figure.
[Figure 2-6] Connection of equipotential terminal
Connected peripheral devices should comply with IEC standards (Data

processing equipment is IEC60950/EN60950, medical equipment is IEC60601-
1/EN60601-1).
Also, all components of the product must comply with IEC60601-1-1/EN60601-1-
1, system specification. A person who adds peripheral devices to signal input or
output part of the medical device must check if peripheral devices must comply
with IEC60601-1-1/EN60601-1-1 standard.
．．．．．．．
WARNING
 If an external recording device and monitoring devices are properly grounded are not

properly grounded, there is a risk of electrical shock.
 Do not open the cover of the product. Dangerous voltage flows inside the product.
You should conduct part replacement or internal repair of the product in the global
service group of Samsung Medison.
 Always check exterior, cable, cord and plug etc. of the product before use.
If there is damage to the exterior such as cracks on the surface or breaking or the
cable is worn, stop using and disconnect power.
 When cleaning the product, unplug the power cord all the time.
 Before using the high voltage heart massage device, you should isolate all devices
(example, probe, ECG lead) in contact with patients.
 Do not use the product in a place where there is flammable gas or anesthetic gas.
There is a risk of explosion.
 Do not install the product in a place where power is difficult to be shut off.
．．．．．．．
CAUTION
 The system was produced for 100-120VAC and 200-240VAC and you can use monitor,
printer and VCR by selecting power of Outlet.
Before connecting the power cord of peripheral devices, check if the voltage of
peripheral devices and voltage of power cord to be connected match each other.
 Installation of insulation transformer protects the product from Surge voltage. Installation
of insulation continues to operate even when the product is in standby.
 Do not soak the power cord in liquid. The power cord is not waterproof.
 Subsidiary socket Outlet of this product is for 100-120VAC and 200-240VAC with the
maximum output of 200W. Also, this subsidiary socket Outlet is only used to supply
power to equipment forming the part of the ultrasound system so do not connect
multiple-tap or extension cord etc. additionally.
 Do not operate input and output terminals (SIP/SOP) on the back of the product while
diagnosing a patient. Electrical shock due to leakage current may occur.
1.3.2 ECG related matters

．．．．．．．
WARNING
 This product does not provide ECG monitoring function. Therefore, inadequate ECG
signal is not recognized.
 Do not use ECG electrodes for HF surgical equipment. There is a risk of fire due to
damage of HF surgical equipment.

Service Manual
 Do not use ECG electrodes while using Cardiac Pacemaker or other electrical
stimulation devices.
 Do not use ECG electrodes and leads in the operating room.
1.3.3 ESD
Generally, ESD (Electro Static Discharge) is the electrostatic phenomenon that
may occur due to friction in the natural state. ESD occurs the most frequently in a
dry state or the heater or air conditioner is running.
ESD occurs in the process that electricity generated from charged objects charges
less charged or not electrically charged objects.
That is, it may occur when a person touches a metal doorknob, file cabinet,
computer and even other people.
[Figure 2-7] ESD label
．．．．．．．
CAUTION
 Static electricity caused to users or patients of the product may damage to probe and
ultrasound system from time to time.
 Before using the connector on which ESD warning symbol is marked, be sure to
conduct precautionary procedures.
- Put on antistatic spray to carpet or linoleum.
- Use antistatic mat.
- Earth the product between a patient table or bed.
 We recommend that those involved in product use receive education on ESD related
warning signs and precautionary procedures.
1.3.4 EMI
This product passed the standards of Electro Magnetic Interference (EMI).
However, if using the product in the electromagnetic field, the quality of ultrasound
imaging may decline or cause damage to the product. If the quality of ultrasound

imaging decline significantly or there is a problem, check if there is a device
generating electromagnetic waves around the place where the product is used.
Electromagnetic radiation may occur from a nearby place or the same space
and mobile phone, beeper, or nearby radio, TV or microwave oven etc. are the
representative causes of electromagnetic waves.
．．．．．．．
CAUTION
If operation of the system is not smooth due to electromagnetic waves, move EMI
to a place far away from EMI.
1.3.5 EMC
EMC(Electro Magnetic Compatibility) test of this product was conducted according
to IEC60601-1-2, International standard for medical equipment. In Europe, IEC
standard was selected as European standard (EN60601-1-2).
1.3.5.1 Guidance and manufacturer declaration – Electromagnetic Emission

This product is used the electromagnetic environment as follows. A user should
check if this product is used in the following environment.
Emission test Compliance Electromagnetic environment -guidance
The Ultrasound System uses RF energy only for

RF Emission its internal function. Therefore, its RF emissions
Group 1
CISPR 11 are very low and are not likely to cause any
interference in nearby electronic equipment.
RF Emission
Class B
CISPR 11
The Ultrasound System is suitable for use in all
establishments, including domestic
Harmonic Emission
Class A establishments and those directly connected to
IEC 61000-3-2
the public low-voltage power supply network that
supplies building used for domestic purpose.
Flicker Emission
Complies
IEC 61000-3-3

Service Manual
1.3.5.2 EMC approved cable, probe and peripheral devices

1) Cable
Cable connected to this product may affect electromagnetic emissions of the
product.
Therefore, only use cables suitable for types and length presented below
Cable Type Length
VGA Shielded Normal

RS232C Shielded Normal
USB Shielded Normal
LAN(RJ45) Twisted pair Any
S-Video Shielded Normal
Foot Switch Shielded 2.5m
B/W Printer Unshielded Coaxial Normal
MIC Unshielded Any
Printer Remote Unshielded Any
Audio R.L Shielded Normal
VHS Shielded Normal
ECG AUX input Shielded < 3m
Parallel Shielded Normal
2) Probe
Probes written in ‘Chapter 9, probe’ of this service manual passed the test
conforming withGroup1 Class B required in international standard CISPR 11.
3) Peripheral devices
Peripheral devices used in this product may affect electromagnetic emissions.
．．．．．．．
CAUTION
• If connecting peripherals that a user has like Remote Printer,
checking the electromagnetic compatibility of the product is the obligation of the
user. Only use devices suitable for CISPR 11 or CISPR 22, CLASS B.
．．．．．．．
WARNING
• Use of unauthorized cables, probe, peripherals may increase emissions
of electromagnetic waves or may decrease tolerance of ultrasonic products.

IEC 60601 Electromagnetic
Immunity test Compliance level
Test level environment -guidance
Floors should be wood,

Electrostatic ±6KV Contact ±6KV Contact concrete or ceramic tile. If
floors are covered with
discharge (ESD)
±8KV air ±8KV air synthetic material, the
IEC 61000-4-2 relative humidity should
be at least 30%.
Electrical fast Mains power quality

±2KV for power ±2KV for power
should be that of a typical
transient/burst supply lines supply lines
commercial or hospital
±1KV for input/output ±1KV for input/ environment.
lines output lines
IEC 61000-4-4
Surge Mains power quality

±1KV differential
±1KV differential mode should be that of a typical
IEC 61000-4-5 mode
±2KV common mode commercial or hospital
±2KV common mode
environment.
Voltage dips, <5% Uт <5% Uт Mains power quality
short (>95% dip in Uт) (>95% dip in Uт) should be that of a typical
interruptions and for 0.5cycle for 0.5cycle commercial or hospital
voltage variations environment. If the user of
on power supply 40% Uт 40% Uт this product requires
input lines (60% dip in Uт ) (60% dip in Uт ) continued operation
for 5 cycle for 5 cycle during power mains
IEC 61000-4-11 interruptions, it is
70% Uт 70% Uт recommended that this
(30% dip in Uт) (30% dip in Uт) product be powered from
for 25 cycle for 25 cycle an uninterruptible power
supply or a battery.
<5% Uт <5% Uт
(<95% dip in Uт ) (<95% dip in Uт )
for 5 s for 5 s
Power frequency Power frequency
(50/60Hz) magnetic fields should be
magnetic field at levels characteristic of a
3 A/m 3 A/m
typical location in a typical
IEC 61000-4-8 commercial or hospital
environment.
NOTE Uт is the a.c. mains voltage prior to application of the test level.

Service Manual
Conducted RF 3 Vrms 0.01V Portable and mobile RF

communications equipment should be
IEC 61000-4-6 150 kHz to 80MHz
used no closer to any part of the
Ultrasound System, including cables,
than the recommended separation
distance calculated from the equation
applicable to the frequency of the
transmitter.
Recommended separation distance
80MHz to
800MHZ
800MHz to
2.5GHz
Radiated RF 3 V/m 3 V/m Where P is the maximum output
power rating of the transmitter in watts
IEC 61000-4-3 80 MHz to 2.5GHz (W) according to the transmitter
manufacturer and d is the
recommended separation distance in
meters (m).
Field strengths from fixed RF

transmitters, as deter-mined by an
electromagnetic site survey, a should
be less than the compliance level in
each frequency range. b
Interference may occur in the vicinity

of equipment marked with the
following symbol :
NOTE 1) At 80MHz and 800MHz, the higher frequency range applies.

NOTE 2) These guidelines may not apply in all situations. Electromagnetic propagation is affected by
absorption and reflection from structures, objects and people.
a Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless)
telephones and land mobile radios, amateur radio, AM and FM radio broadcast and TV broadcast
cannot be predicted theoretically with accuracy. To assess the electromagnetic environment due to
fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field
strength in the location in which the Ultrasound System is used exceeds the applicable RF
compliance level above, the Ultrasound System should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such as re-orienting or
relocating the Ultrasound System or using a shielded location with a higher RF shielding
effectiveness and filter attenuation.
b Over the frequency range 150kHz to 80MHz, field strengths should be less than [V 1 ] V/m.

1.3.5.3 Recommended spacing between radio frequency communication
device and ACCUVIX A30
This product is used in the electromagnetic environment where radiated radio
frequency interference is adjusted. The user can prevent electromagnetic
interference by maintaining the minimum distance with portable
radio frequency communication device (transmitter) and adjusting the maximum
output of communication device as follows.
Separation distance according to frequency of transmitter [m]
800MHz to
Rated maximum 150kHz to 80MHz 80MHz to 800MHz
2.5GHz
output power of
transmitter
[W]
V 1 =0.01Vrms E 1 =3 V/m E 1 =3V/m
0.01 35.00 0.11 0.23

0.1 110.68 0.36 0.73
1 350.00 1.16 2.33
10 1106.80 3.68 7.37
100 3500.00 11.66 23.33
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be estimated using the equation applicable to the
frequency of the transmitter, where p is the maximum output power rating of the
transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1) At 80MHz and 800MHz, the separation distance for the higher frequency range
applies.
NOTE 2) These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
1.3.5.4 Electromagnetic environment – guidance

Ultrasound Products should be used in the blocked space with minimum radio
frequency blocking effect and connected to a place where cables are
shielded. Field strength of fixed radio-frequency transmitter, as determined by
electromagnetic test, should be lower than 3V/m at the outside of blocked
space. Mandatory checks are performed to verify that the actual blocking effect of
blocked space and attenuation of filter conform with the least provisions.
．．．．．．．
CAUTION
If connecting remote devices that users hold such as Remote Printer or LAN,

Service Manual
Samsung Medison is not responsible for problems caused in the presence of the
electromagnetic phenomenon.
1.3.5.5 Avoiding electromagnetic interference
The phenomena of electromagnetic interference that may occur in each diagnostic
mode are as follows.
1 2 3
Imaging Mode ESD RF Power Line
Change of operating For sector imaging White dots,
mode, system probes, white radial dashes, diagonal
settings, or system bands or flashes in the lines, or diagonal
reset. centerlines of the lines near the
Brief flashes in the image. center of the
2D displayed or recorded For linear imaging image.
image. probes, white vertical
bands, sometimes
more pronounced on
the sides of the image.
Increase in the image White dots,
background noise or dashes, diagonal
M white M mode lines. lines, or increase
in image
background noise
Color flashes, radial or Color flashes,
vertical bands, increase dots, dashes, or
Color in background noise, or changes in the
changes in color image. color noise level.
Horizontal lines in the Vertical lines in
spectral display or the spectral
Doppler tones, abnormal noise display, popping
in the audio, or both. type noise in the
audio, or both.
1. ESD caused by discharging of electric charge build-up on insulated surfaces or

persons.
2. RF energy from RF transmitting equipment such as portable phones, hand-held
radios, wireless devices, commercial radio and TV, and so on.
3. Conducted interference on power lines or connected cables caused by other
equipment, such as switching power supplies, electrical controls, and natural
phenomena such as lightning.
Medical devices may cause electromagnetic interference or be affected

by electromagnetic interference. EMC standards represent tests
on electromagnetic interference generated or accepted. Electromagnetic
interference generated in ultrasound products of Samsung Medison does not
exceed the reference standards. Designed to receive radio-frequency
signals, ultrasound products are likely to be interfered by energy source of radio
frequency. Other examples of causing interference are medical equipment,
IT products, transmission tower of radio and TV etc. Since there are difficulties

in finding interference causes, users must find interference causes by considering
the following.
 Is electromagnetic interference intermittent or continuous?
 In the same frequency, does electromagnetic interference appear one probe or
several probes?
 Does the same problem occur when two different probes are used in different
probe?
 Does electromagnetic interference occur even when
moving ultrasound products to another place?
The answers to the above items tell you that which one is the problem between
ultrasound products or the use environment of products.
After answering each item, please contact Samsung Medison Global Service
Group in your area.

Service Manual
1.4 Mechanical safety
1.4.1 Precautions for moving

．．．．．．．
WARNING
The weight of the product is more than 100kg so be very careful when moving. If
moving the product carelessly, it may cause injury to users or damage to
product.Before moving, check if moving locking device of the front wheels is
unlocked. Also, fix it not to move by completely folding the arm of the monitor. Be
sure to transport the products lowly by using the handle on the back of console.
This product has the durability for shocks. However, excessive shock such as fall
of the product etc. may cause serious damage. If the product does not operate
normally after moving, contact Samsung Medison Global Service Group.
1.4.1.1 Moving locking device

It is attached to only front wheels. To lock, press the upper part of locking device
with your foot. To unlock, press off part under locking device with your foot. You
can control the movement of the product with this device.
It is convenient to use the product in locking state while using it.
1.4.1.2 Precautions on the slope

Be sure to transport it by pointing control panel in the direction you want to move
．．．．．．．
WARNING
When moving this product, pay attention to the movement of wheels. We
recommend you to practice in advance when climbing or descending the slope.
When stopping the product on the slop for a moment, the product may fall even if
locking moving locking device.
Do not stand it on the slope if possible.

1.4.2 Precautions for use
．．．．．．．
CAUTION
 Do not apply excessive force to control panel.
 Never use the product by converting it
 If reusing the product while not using it for a long time, check safe operation before use.
 Be careful for foreign substances, especially metal pieces not to enter the product.
 Be careful not to obstruct the ventilation window of the product.
 When unplugging the power cord, do not unplug holding the cord. Cord may be
damaged and it can cause short circuit or disconnection. Be sure to unplug holding a
plug.
 If excessively tying or twisting cable connected to patients, the product may stop
operation or cause malfunction.
 If cleaning or disinfecting the part connected to a patient inadequately, the product may
cause a malfunction. For detailed description on cleaning and disinfection related to
protection of the product, see ‘Chapter 8, Maintenance and storage’.
1.4.2.1 Precautions while using monitor

If adjusting the height or position of monitor, note the space between monitor arms.
You may get injured because your finger etc. may get stuck.
[Figure 2-8] Precautions while using monitor

Service Manual
1.4.2.2 Precautions while using control panel
．．．．．．．
CAUTION
 Do not push control panel with excessive force or lean against it.
 Do not sit on control panel or apply excessive force.
If adjusting the height or position of control panel, note the space between control
panel and lift. You may get injured because your finger etc. may get stuck.
[Figure 2-9] Precautions while using control panel

1.5 Biological safety
For safety matters on probe, biopsy, see ‘Chapter 9, probe’ of this manual.
．．．．．．．
WARNING
 Ultrasonic waves may cause harmful effects in cells and be potentially harmful to
patients. When there is no special purpose medically, minimize the exposure time and
maintain the output of ultrasonic waves as low as possible. See ALARA principle.
 If an error message or warning message on dangerous situations appears on the screen
of the product, do not use the product. Write down the on-screen message and then turn
off power and contact the Samsung Medison Global service group.
 Do not use showing abnormal and strange behavior. Discontinuous operation of
continuous scanning is due to failure of hardware and it should be repaired prior to use.
 This product limits the temperature that a patient can touch to less than 43
degrees Celsius and Ultrasonic power output (AP&I) complies with the limits of U.S. FDA.
1.5.1 ALARA principle

Diagnosis through ultrasound equipment can be done with the principle, ‘As Low
As Reasonably Achievable.’ Many people have discussed and defined about
what is 'reasonable'. However, there are no rules like perfect formula which is
suitable for all environments and can control situations. But when diagnosing, by
being minimally exposed to ultrasound waves, the damage caused by ultrasound
waves can be reduced. Because the damage caused by ultrasound waves has
not been identified yet, it is very important to adjust the amount of ultrasound
waves penetrated to patients. Therefore, it is important to obtain accurate images
by ultrasound diagnosis but it is also important to reduce the exposure time of
patients. For harmony between exposure time of patients and obtaining accurate
images, the ultrasound system provides the function to adjust test results in
optimal status while diagnosing. The ability to always understand and fulfill ALARA
principle is very important. The development of ultrasound diagnosis is possible
because ultrasound device as well as technology providing information of high
quality is being developed. This major information is made based on several
output data of ultrasound waves and plays an important role in implementing the
principle of ALARA. There are many variables affecting output data, basic data of
provided information. They are mass, size, the position of bones related to focus,
weakness of the body and time to exposed ultrasound waves etc. Among them,
exposure time is the variable requiring the most attention. Because unlike other
variables, exposure time is the variable determined by users of ultrasound
equipment.

Service Manual
1.5.1.1 Applying ALARA

Imaging mode of the system used varies depends on the information you
need. While 2Dmode and M mode images provide anatomical information,
Doppler, power and color mode images provide blood flow information. While
scanned mode such as 2D mode, power or color distributes ultrasound energy by
dispersing ultrasound energy across area, unscanned mode such as M mode or
Doppler focuses ultrasound energy. By understanding the characteristics of
imaging mode being used, ultrasound users form ajudgment based on information
by applying ALARA principle. And due to added probe frequency, system setting
value, scanning technology and operator experience, users will be able to comply
with ALARA principle. The amount of Acoustic output is determined by the system
operator in the final analysis. This decision should be based on factors such as
type of patient, kind of experiment, patient history, easy accessibility
on useful diagnostic information, potential heat applied to the patient's local part
from probe surface temperature etc. For correct diagnostic results, patient
exposure is limited to the lowest index for required time and the system is
used. Although high index value does not mean the actual occurrence of Bio
effect, if index value is high, this is the problem that should be handled carefully. It
means that every effort should be put to reduce the negative impact that high
index value may cause. Limiting exposure time may be one kind of effective
method. There are several system controls that can be used by users to adjust
image quality and limit Acoustic intensity. These controls are related to skills
needed for operator to implement ALARA and are classified into 3 categories,
direct, indirect, receiver control.
1.5.1.2 Direct Controls

Selection of diagnostic subjects and Output intensity control affect Acoustic
intensity directly. Depending on the selection, acceptable range of Intensity or
Output varies. Selecting the accurate Acoustic intensity range for diagnostic
subjects is one of priorities that should be considered in any experiment. For
example, peripheral vascular intensity level is not recommended
in fetal experiments. Some systems automatically select the appropriate range of
specific diagnostic subjects and other diagnostic subjects should be directly
selected by users manually. Ultimately, users should be responsible
for appropriate clinical use of the product. The system of Samsung Medison
provides both basically provided automatic setting and selectable manual setting.
Output affects Acoustic intensity directly. Once diagnostic subjects are set, Output
control can be used to raise or lower Intensity output. Through Output control,
Intensity level can be selected lower than the highest setting. If using carefully,
you can always select excellent image quality and minimum Output intensity.

1.5.1.3 Indirect Controls
Indirect controls have an indirect effect on Acoustic intensity and mainly affect
imaging mode, pulse repetition frequency, focal depth, pulse length, probe
selection etc. The characteristics of ultrasound beam are determined depending
on the choice of image mode. 2D mode is scan mode and Doppler mode is stop
or unscanned mode. Stop ultrasound beam focuses energy to one place. Moving
or scan ultrasound beam disperses energy across area and is focused on the
same area only for a fraction of unscanned mode time. Pulse repetition frequency
or repetition rate represents the number of ultrasonic blast of energy occurring
during a period of time. As pulse repetition frequency gets higher, pulse of energy
during a period of time increases more. Some kinds of controls as follows affect
pulse repetition frequency: focal depth, display depth, sample volume depth, color
sensitivity, number of focal zones and sector width controls etc. Focus of
ultrasound beam affect resolution of images. To maintain or improve resolution
in several focuses, various outputs on focal zone are necessary and this is one of
system optimization functions. Several experiments require different focal depth. If
adjusting the focus to the appropriate depth, resolution is improved. Pulse length
is the time while ultrasound waves are generated. The longer pulse is, the greater
time-average intensity value is. As Time-average intensity increases, the
possibility of cavitation and temperature rise will be greater. Pulse length
or ultrasonic generation length or pulse duration time is Output pulse duration time
in Pulsed Doppler. Also, if raising Doppler sample volume, pulse length also
increases. Probe selection also has an indirect effect on Intensity. Tissue
attenuation changes according to frequency control. The higher probe operating
frequency is, the greater attenuation of ultrasound energy is. If probe operating
frequency gets higher, stronger Output intensity is necessary when scanning in
the deeper place. To scan more deeply in the same Output intensity, lower probe
frequency is required. Therefore, using Gain and Output more than necessary
means that lower frequency probe is necessary
without corresponding improvement in image quality.
1.5.1.4 Receiver Controls

When trying to improve image quality, the user uses receive controls. These
controls have no effect on Output. Receiver controls only affect the method that
ultrasound Echo is received. These controls are Gain, TGC, Dynamic range and
image processing. One thing to keep in mind with respect to Output is that
receiver controls should be optimized before Output increases. For example, by
optimizing Gain before increasing Output, you should improve image quality.

Service Manual
1.5.1.5 Additional Considerations

The shortest scanning time should be maintained and scanning should be done
only for medical purposes. Try to avoid compromising with Quality hastening the
experiment. Insufficient experiments require further reinforcement and ultimately, it
results in time delay. Diagnostic ultrasound waves are one of important tools in the
field of medicine and should be used efficiently and effectively as with other tools.
1.5.1.6 Output Display Features

System Output display is composed of two basic indices, mechanical index and
temperature index. Again, thermal index is divided into soft tissue (TIs), bone (TIb)
and skull (TIc). Among 3 kinds, one thermal index is always displayed on the
screen. Which one is displayed is determined depending on close diagnostic
subjects and by user choice or system setting. Mechanical index increases in 0.1
unit in the range of 0.0 to 1.9 and is displayed continuously. Thermal index is
composed of 3 indices and only one thing is always displayed among them. Each
probe diagnostic subject has suitable selection suitable for the combination. TIb or
Tis is continuously displayed from 0.0 to maximum Output based on the probe
and diagnostic subjects and increment is 0.1. It is an important factor of characteristic
index reaction according to diagnostic subjects of default setting. Default setting is System
control state and is set in advance by manufacturers and operators.
The system has basic index setting for probe diagnostic subjects. This default setting is
automatically read by the ultrasound system when new patient data is entered into system
database or diagnostic subjects are changed. Among 3 thermal indices, which index
will be displayed is determined based on the following categories.
Index appropriate for diagnostic subjects: Tis is used for soft tissue image and TIb
is used for bones or focus near bones. It relieves the factors artificially raising or
lowering temperature index records such as position of bone or fluid or flow of
blood. For example, this is the case that practical possibility for local heating is
lower than thermal index display due to rapidly attenuating tissue path.
Unscanned mode operation compared to probe mode affects temperature
index. In case of scan mode, the heating possibility increases as closer to the
surface and in case of unscanned mode, the heating possibility increases as
deeper to Focal zone.
Always limit ultrasound exposure time. Do not hurry the experiment. Maintain the
index to the minimum and always limit exposure time without compromise with
Diagnostic sensitivity.

1) Mechanical Index (MI) Display
The mechanical biological effect is the beginning phenomenon occurring when

Output of a certain level was exceeded. However, the beginning level changes
depending on the type of tissues. The possibility of mechanical biological effect
changes depending on Peak pressure and ultrasound index. MI explains these
two factors. The higher MI value is, the greater the possibility of occurrence of a
mechanical biological effect is. There is no specific MI value showing
that mechanical effects are actually occurring. MI should be used only
as guidance to implement ALARA principle.
2) Thermal Index (TI) Display
TI tells users the possibility of temperature rise which is present in the focus
above the bone of ultrasound beam or Body tissue or the surface of the body. TI is
temperature rise expectation in characteristic body tissues. The
substantial amount of temperature rise is affected by factors such as kinds of
tissues, Vascularity, operating mode etc. Because TI is used only as the basic
guideline to implement ALARA principle. Thermal index of bones(TIb), for example,
tells users potential heating that may occur in or near the focus after ultrasound
beam passes through Fluid or soft tissue such as 2-3 month-
old fetus skeleton. Skull thermal index (TIc), for example, tells you potential
heating of bones that may occur on the surface of skull etc. or near it. Body
tissue thermal index (TIs) tells you potential heating that may occur in Soft
homogeneous tissue. In Miscellaneous system setting, you can select Tis or Tib
by using TIs/TIb selection. Tic is displayed if you select Trans cranial application.
3) Mechanical and Thermal indices Display Precision and Accuracy
MI and TI precision is shown in 0.1 unit in the system. Accuracy estimate of MI
and TI display on the system can be found in Acoustic Output Tables manual. This
accuracy estimate is based on changeable range of probe and system, unique
Acoustic output modeling errors and measurement variability and is as follows.
Displayed values should be construed as related information helping system
operator to conduct according to the principles by using the system carefully.
The values should not be construed as the actual physical value in tissues or
organs in question. The initial data used to support Output display are
from laboratory measurement criteria based on AIUM measurement
standards and these measurement criteria are applied to algorithm to calculate
Output values to be displayed. Many assumptions used in the process of
measurement and calculation are essentially conservative. Over-estimation of
substantial in situ exposure on numerous tissue paths is included in the
measurement and calculation process. For example, measured water tank values
are depreciated by considering the mutual attenuation effect of 0.3dB/cm-MHz,
the conservative industrial standard. The conservative value for tissue features
was selected to be used in TI model. Conservative value for absorption rate of
tissue or bone, blood perfusion rates, blood heat capacity and
tissue temperature conductivity etc. are included.

Service Manual
Steady state temperature rise is estimated in industry-standard TI model and this

assumes that ultrasound probe lay in one place long enough to be considered that
it is steady state. When evaluating the accuracy of display values, numerous
factors are considered.
Among them, hardware change, evaluation algorithm accuracy
and measurement variability, variability between probe and system are important
factors. Probe variability is shown as the result of sensitive lens focusing on
parameter changes, Process-related impedance differences and Crystal
efficiencies of Piezoelectric. Differences in efficiency and system pulse voltage
control also affect changes. Algorithm has its unique uncertainty in predicting
Acoustic output value exceeding the range of Pulser voltages and possible
system operating conditions.
Inaccuracy of measurement criteria are related to the differences between
Hydrophone calibration and function, location, sorting and digitizing tolerance and
test operators. Conservative assumption on Output prediction algorithm of Linear
propagation through attenuation media of 0.3dB/cm-MHz is not considered
in measuring the accuracy of the display in any depth. The same attenuation
in 0.3dB/cm-MHz or linear propagation also does not occur in water tank
measurement or tissue paths of most of the body.
In the body, various tissues and organs have different attenuation characteristics.
But, there is little attenuation in water. In the body and water tank measurement,
when Pulser voltages rise, linear propagation and Saturation losses
occur. Display accuracy estimation is based on probe and systems,
unique Acoustic output modeling error and variation range of measurement
variability. Display accuracy estimation is measured based on AIUM measurement
criteria but not based on nonlinear loss effect for measured values or Error caused
by measurement.
1.5.1.7 Control effect- Control Affecting the indices

When various system controls are adjusted, TI and MI values may be changed.
While this is the most clearly revealed when power control is adjusted, other
system controls affect On-screen output values.
1) POWER
Power controls system Acoustic output. 2 real time Output values of TI and MI
appear on the screen. These change as the system responds to power
adjustment. In combination modes such as simultaneous color, 2D mode, Pulsed
Doppler, all of each mode is added to total TI. Each mode is the major factor of
this total TI and displayed MI appears from the mode with the largest peak
pressure.

Service Manual
1.5.1.8 2D mode Controls

1) 2D mode size
Frame rate will rise if narrowing Sector angle. Then, TI also increases. Pulser
voltage is automatically adjusted low with software control so TI is maintained to
less than system maximum. Decrease of Pulser voltage decreases MI.
2) ZOOM
If enlarging images, Frame rate will rise. Then, TI also increases. To improve
resolution, the number of Focal zones will increase automatically. The highest
Intensity may occur at different depths so this will bring the change of MI.
3) Persistence
As persistence is lower, TI will decrease. Pulser voltage will rise automatically.
Rise of Pulser voltage will raise MI.
4) Focal no.
If there are many Focal zones, frame depth or focal depth is automatically
changed and therefore, both TI and MI are changed. As Frame rates are lower, TI
decreases. Displayed MI will respond to the area that will be the highest Intensity.
5) FOCUS
If changing focal depth, MI is changed. In general, when focal depth is close to
natural focus of Transducer, MI value will be higher.
1.5.1.9 Color and Power Controls

1) Color Sensitivity
If increasing color sensitivity, TI rises and more time is consumed to scan color
image. Color pulses are the main pulse type in this mode.
2) Color Sector Width
If narrowing color sector width, color Frame rate rises and TI also increases. The
system lowers Pulser voltage automatically and maintains it to less than the
maximum. If lowering Pulser voltage, MI decreases. If Pulsed Doppler is also
being operated, Pulsed Doppler will maintain the main mode and the change of TI
will be small.
3) Color Sector Depth
If color sector depth is deepened, color Frame rate will be reduced automatically
or new color focal area or color pulse length will be selected. TI will change by
the combination of these effects. In general, color sector depth increase, TI
decreases. MI will respond to the highest Intensity of the main pulse type, color
pulse. However, if Pulsed Doppler is also operating, Pulsed Doppler will maintain
the main mode and change of TI will be small.

4) SCALE
If increasing Color velocity range by using scale control, TI may increase. The
system will be adjusted automatically to keep Pulser voltage less than system
maximum. Decrease of Pulser voltage also decreases MI.
5) SEC WIDTH
If narrowing 2D mode sector width in color images, color Frame rate rises. TI will
increase and MI will not change. If Pulsed Doppler is operating, Pulsed Doppler
will maintain the main mode and the change of TI will be small.
1.5.1.10 M mode and Doppler Controls

1) Speed
M Mode and Doppler Sweep speed adjustments will not affect MI. If M mode
Sweep speed changes, TI will change.
2) Simultaneous and Update Methods
If using Combination modes, both TI and MI are affected through combination of
pulse types. During Simultaneous function, TI will be Additive. During Auto-update
and Duplex, TI will display main pulse types. Displayed MI will come from the
mode with the highest maximum pressure.
3) Sample Volume Depth
When Doppler sample volume depth increases, Doppler PRF
is automatically lowered. If PRF is lowered, TI will also decrease. System will
maintain Pulser voltage to less than the system maximum by automatically
lowering it. Decrease of Pulser voltage decreases MI.
1.5.1.11 Doppler, CW, M-mode, and Color Imaging Controls

When new image mode was selected, both TI and MI will be changed into default
settings. Each mode has corresponding pulse repetition frequency and
maximum Intensity point. In combined or simultaneous mode, TI is the sum of
Contribution from operated mode and MI is MI for focal area and mode with
intensity of the greatest derated rate. If mode is turned off and selected again, the
system will go back to the mode of previous state.
1) Probe
Each useful probe model has unique specification for contact area, beam shape
and center frequency. When selecting probe, default values are initialized.
MEDISON plant default values differ depending on probe, diagnostic subject and
selection mode. Default values are selected as less than the standard of

Service Manual
FDA depending on the use.

2) DEPTH
Increase of 2D mode depth automatically lowers 2D mode Frame rate. This will
reduce TI. The system will automatically select deeper 2D mode focal depth. The
change of focal depth will cause the change of MI. Displayed MI is MI of the area
with the largest Intensity.
3) Application
Acoustic output default values are set when selecting diagnostic subject.
MEDISON plant default values differ depending on probe, diagnostic subject and
selected mode. Default values are selected as less than the standard of
FDA depending on the use.
1.5.1.12 Related Guidance Documents

For more information on ultrasound biological effects and related topics, see the
following;
AIUM Report, January 28, 1993, “Bio effects and Safety of Diagnostic Ultrasound”
Bio effects Considerations for the Safety of Diagnostic Ultrasound, J Ultrasound
Med., Sept.1998: Vol. 7, No. 9 Supplement
Acoustic Output Measurement Standard for Diagnostic Ultrasound Equipment.
(AIUM, NEMA. 1998)
Acoustic Output Labeling Standard for Diagnostic Ultrasound Equipment (AIUM,
1998)
Second Edition of the AIUM Output Display Standard Brochure, Dated March 10,
1994. (A copy of this document is shipped with each system.)
Information for Manufacturer Seeking Marketing Clearance of Diagnostic
Ultrasound Systems and Transducers. FDA. September 1997. FDA.
Standard for Real-Time Display of Thermal and Mechanical Acoustic Output
Indices on Diagnostic Ultrasound Equipment. (Revision 1, AIUM, NEMA. 1998)
WFUMB. Symposium on Safety of Ultrasound in Medicine: Conclusions and
Recommendations on Thermal and Non-Thermal Mechanisms for Biological
Effects of Ultrasound, Ultrasound in Medicine and Biology, 1998: Vol. 24,
Supplement1.
1.5.1.13 Acoustic Output and Measurement

Since diagnostic ultrasound is used for the first time, research on Bio effects of
human that may be caused due to exposure to ultrasound waves has been
conducted in numerous scientific and medical laboratories. In October 1987, the

American Institute of Ultrasound in Medicine(AIUM) approved the reported
prepared by Bio effects Committee (Bio effects Considerations for the Safety of
Diagnostic Ultrasound, J Ultrasound Med., Sept. 1988: Vol.7, No.9 Supplement)
and it is often called as Stowe Report and is the report that reviewed useful data
on the possible effects of ultrasound exposure. Another report, “Bio effects and Safety of
Diagnostic Ultrasound” provides more current information as of January 28,
1993. Acoustic output on this system was measured and calculated based on
December 1985 “510(K) Guided for Measuring and Reporting Acoustic Output of
Diagnostic Ultrasound Medical Devices but only Hydrophone complies with the
requirements of Acoustic Output Measurement Standard for Diagnostic Ultrasound
Equipment” (NEMA UD 2-1992).
1.5.1.14 In Situ, Derated and Water Value Intensities

All Intensity parameters are measured in water. Since water does not absorb
Acoustic energy, this water measurement represents the worst value. Biological
tissues do not absorb Acoustic energy. In any aspect, true value of Intensity differs
depending on the amount and type of tissues and the frequency of ultrasound
waves passing through the tissues. In Situ, intensity value in tissues, intensity
value in tissues has been measured in accordance with the following equation:
In Situ = Water [ e − ( 0.23alf ) ]

where: In Situ = In Situ Intensity Value
Water = Water Value Intensity
e = 2.7183
a = Attenuation Factor
Tissue a(dB/cm-MHz)
Brain .53
Heart .66
Kidney .79
Liver .43
Muscle .55
l = skin line to measurement depth (cm)
f = center frequency of transducer/system/mode combination (MHz)
Since ultrasound waves are likely to pass through tissues whose length and type
are changed during the experiment, it is difficult to predict true In Situ intensity.
If attenuation

Service Manual
factor is 0.3, it is used as the general reporting purpose;

Therefore, In Situ value usually reported uses the following equation:
In Situ (derated) = Water [ e − ( 0.069lf ) ]

Since this value is not true In Situ intensity, the term, “Derated” is used.
Despite the same operating conditions, maximum Derated and maximum water
values do not always occur. Therefore, reported maximum water values and
Derated values may not be related to In Situ (Derated) equation. Multi-zone array
transducer with maximum water values Intensities in the deepest area is the
example. The same transducer may have the greatest Derated intensity in one of
the shallowest focal areas.
1.5.1.15 Acoustic Output and measurement

The terms and symbols used on Acoustic output table are defined in the following
paragraph.
ISPTA.3 Derated spatial-peak temporal-average intensity (Milliwatts per square

centimeter).
ISPPA.3 The derated spartial-peak pulse-average intensity
(Watts per square centimeter).
If Global maximum MI is reported, the value of IPA.3 may be reported
instead of ISSPPA.3 in the position of Global maximum MI(IPA.3@MI).
MI If The Mechanical Index. ISPPA.3 is 190W/cm2, the value of MI,
(MI@ISPPA.3) may be reported instead of MI(Global maximum value) in the
position of ISPPA.3.
Pr.3 Derated peak rare factional pressure combined with Transmit pattern which
is the source of values reported as less than MI (Megapascals).
WO Ultrasonic power (Milliwatts). WO is total Time-average power for operating
conditions which is the source of ISPTA.3;
For operating conditions supposed to be reported as less than ISPPA.3, WO
is Ultrasonic power combined with Transmit pattern which is the source of
value reported as less than ISPPA.3.
Fc Center frequency (MHz).
For MI and ISPPA.3, fc is Center frequency combined with Transmit pattern
which is the source of Global maximum value each parameter.
For ISPTA.3, for Combined modes accompanying other Center
frequency, fc is defined as the whole range of center frequencies of each

Transmit patterns.
ZSP Axis distance that reported parameters will be measured (Centimeters).
x-6,y-6 This is In-plane (Azimuthal) and Out-of-plane (Elevational) -6 dimensions,
respectively in X-Y plane where Zsp is founded.
PD pulse duration combined with Transmit pattern which is the source the values
reported of each parameter (Pulse duration) (1/1000000 second unit).
PRF Pulse combined with Transmit pattern which is the source of reported values
of each parameter
Pulse repetition frequency) (Hz).
EBD Entrance beam dimensions on Azimuthal and Elevational Planes
(Centimeters).
EDS Entrance dimensions of the scan on Azimuthal and Elevational Planes
(Centimeters).
1.5.1.16 Acoustic Measurement Precision and Uncertainty

Acoustic measurement precision and uncertainty are as follows.
Quantity Precision Total Uncertainty
PII.3 (derated pulse intensity integral) 3.2 % +21 % to - 24 %

Wo (acoustic power) 6.2 % +/- 19 %
Pr.3 (derated rarefaction pressure) 5.4 % +/- 15 %
Fc (center frequency) <1% +/- 4.5 %
1) Systematic Uncertainties
For Pulse intensity integral, Derated rarefaction pressure Pr.3, Center frequency
and Pulseduration, effect screening on accuracy is included in the analysis due
to the following recorded information:
Hydrophone calibration drift or errors.
Hydrophone / Amp frequency response.
Spatial averaging.
Alignment errors.
Voltage measurement accuracy, including.
Oscilloscope vertical accuracy.
Oscilloscope offset accuracy.
Oscilloscope clock accuracy.
Oscilloscope Digitization rates.

Service Manual
Noise.
Acoustic power measurements using systematic uncertainty Radiation Force are

measured by using Calibrated NIST acoustic power sources. Also, as First
supplement on IEC publication 1161, we recommend analytical data in September
1993 conducted by working group of IEC technical committee 87 and prepared by
K. Beissner. This document includes analysis and discussion on source/measure
effects of Error and the causes are
as follows:
Balance system calibration.

Absorbing (or reflecting) target suspension mechanisms.
Linearity of the balance system.
Extrapolation to the moment of switching the ultrasonic transducer (compensation
for ringing and thermal drift).
Target imperfections.
Absorbing (reflecting ) target geometry and finite target size.
Target misalignment.
Ultrasonic transducer misalignment.
Water temperature.
Ultrasonic attenuation and acoustic streaming.
Coupling or shielding foil properties.
Plane-wave assumption.
Environmental influences.
Excitation voltage measurement.
Ultrasonic transducer temperature.
Effects due to nonlinear propagation and saturation loss.
The overall findings of this analysis regards rough Acoustic Power Accuracy figure
as +/- 10% for the frequency range 1 - 10MHz.

1.6 Protection of the environment
．．．．．．．
CAUTION
 Console and peripherals that cannot be used any longer must be handled safely by
requesting the manufacturer to handle them or using proper disposal procedures.
 Waste must be handled in compliance with relevant laws and regulations.
 Global Services Group representative of Samsung Medison or authorized dealer must
replace lithium-ion batteries used in this product.

Chapter 2
About product
Service Manual
Chapter 2 About product
2.1 Overview
Chapter 2 described important information of the product that you basically need to
know before servicing ACCUVIX A30. It explains main functions and configuration of the
product and product specification. ACCUVIX A30 is the color ultrasound diagnostor with
high resolution and deep penetrating power and provides convenient and various
measuring functions.
Contents
2.1 Overview .................................................................................................................. 2-1

2.2 Product configuration .............................................................................................. 2-2
2.2.1 Monitor ....................................................................................................... 2-4
2.2.2 Control Panel............................................................................................. 2-5
2.2.3 Console .................................................................................................... 2-10
2.2.4 Peripheral Devices ................................................................................. 2-12
2.2.5 Probe........................................................................................................ 2-15
2.2.6 Accessory ................................................................................................ 2-16
2.2.7 Option....................................................................................................... 2-16
2.3 Product specification ............................................................................................. 2-17
Chapter 2 About Product 2-1

2.2 Product configuration
ACCUVIX A30 is largely composed of LCD monitor, control panel, console, peripheral
devices, probe etc.
① Monitor
② Monitor Arm
① ③ Keyboard
④ Control panel
② ⑤ Lift
⑥ Probe folder
⑦ DVD Drive
⑧ USB port
⑦ ⑨ Speaker
⑨ ⑩ ECG port
④ ⑪ Probe port
⑫ CW probe port
③ ⑥ ⑬ Air filter
⑭ Moving locking device
⑩ ⑮ Wheel
⑤ ⑧
⑫
⑪
⑬
⑭
⑮
[Figure 2.1 Front of the product]
Chapter 2 about Product 2-2

Service Manual
① Handle
② Storage space
③ Ventilation window
④ USB port and LAN port
⑤ Rear panel
⑥ Cable hook
⑦ Power connecting part
①
②
③
④
⑥ ⑤
[Figure 2.2 Back of the product]

2.2.1 Monitor
LCD monitor is color VGA monitor and shows ultrasound imaging and other information.
You can adjust height and position freely with LCD monitor arm.
[Figure 2-3] Adjusting LCD monitor position]
▐ Screen configuration
The screen of this product is composed of contents such as ultrasound imaging, various
information and menu etc. for users to operate the system. The screen is largely
composed of ① title ② preview ③ imaging ④ Thumbnail ⑤ User Information etc. as
follows.
④
②
③
[Figure 2.4 screen configuration]

Service Manual
 Title area
Patient information, hospital name and diagnostic subject, Frame Rate, depth,probe
information, Acoustic Output information, date and time etc. are displayed.
 Preview area
It shows Thumbnail imaging with preview. If using EZ Exam, EZ Exam menu appears.
 Imaging area
Ultrasound imaging appears. Also, TGC, imaging information,
Annotation, various measurements etc. are displayed.
 Thumbnail area
Maximum 5 images saved by pressing [Save] button are displayed. If pressing Quad
icon, maximum 16 saved images are displayed. If clicking with a pointer, enlarged
image is shown in the image area
 User Information area
A variety of information required while a user uses this system is displayed.The
current state of the system, imaging information, possible selections etc.are displaced.
2.2.2 Control Panel

A user can operate the system through control panel.
[Figure 2.5 control panet]

Control panel is composed of keyboard, soft menu, buttons, dials, dial-button, slide,
track. Dial-Button is an opeartion tool combining dial and button funtions.
▐ Detailed Functions of control panel

The following is description and use methods of various controls in control panel.
After Chapter 3, this manual covers controls with several functions in detail.
Button Turns on/off product power

On/Off
Selects patient ID in the list or Patient Information

Patient Button screen where new patient information can be entered
appears
Probe screen where probe and diagnostic subject can
Probe Button
be selected and changed appears in touch screen.
SONOVIEW Button SONOVIEW, Image Filing program, runs.
The report screen organizing and showing

Report Button
measurements of the diagnostic subject etc. appears.
Finishes Exam of patients being diagnosed and

End Exam Button
resets related data
Button: Starts 2D mode
2D Dial-button
Dial: Adjusts 2D Gain.
Button: starts or ends M mode

M /x Dial-button Dial: adjusts M Gain. It rotates images in the x-axis
direction in 3D view,
Button: starts or ends power Doppler mode.
PD / y Dial-button Dial: adjusts PD Gain. It rotates images in the y-axis
Button: starts or ends PW spectral Doppler mode.
PW / z Dial-button Dial: adjusts PW Gain. It rotates images in the z-axis
Button: Starts or ends color Doppler mode.
Color /
Ref. Slice Dial-button Dial: adjusts C Gain. In 3D View, it moves Reference
Slice from side to side.
3D / 4D Button Starts or ends 3D/4D mode

Service Manual
Button: Starts or ends CW spectral Doppler mode

CW / LR Dial-button Dial: adjusts CW Gain. It adjusts left, right boundary of
ROI in 3D View-MPR. LR stands for Left-Right.
Button: Adjusts the angle of sample volume in spectral

Doppler mode. Also, it is used to adjust the angle of
Angle / TB Dial-button Indicator or probe cursor of body marker.
Dial: Adjusts top, bottom boundary of ROI in 3D View-
MPR. TB stands for Top-Bottom.
Depth Dial-button Adjusts the depth of images that can be observed.
Number and position of focus is changed into the target

Focus Dial-button part to be observed.
Zoom Dial-button Enlarges images
Uses Quick Scan function. ‘Q Scan’ mark is displayed

Q Scan Button at the top of image. It can be used only in particular
diagnostic subjects of particular probe.
Stops images being scanned or activates stopped
Freeze Button
images again.
Save Button Saves images or report of screen in database
Prints the images of screen in the printer connected to

Print Button
the system
Users can use this button by setting the function that

User 1 Button they want. The function of each button is set in Utility >
Setup > User Defined Key
User 2-3 Dial-button they want. The function of each button is set in Utility >
Setup > User Defined Key.
they want. The function of each button is set in Utility >
Setup > User Defined Key.
Button Set: Selects an item or value specified by using
Set / Exit trackball. Or changes the function of trackball.
Exit: Ends the current function and returns to the
previous state
Button In scan mode, the arrow-shaped pointer appears on the screen.

Pointer

Deletes text, Indicator, Body Marker, measurements
Button
Clear etc. displayed on images
Changes into another function that can be supported in

Button
Change the function of current trackball
Button Starts measurement by diagnostic subject

Calculator
Starts basic measurement such as distance,
Button
Caliper volume, circumference and area etc.
Moves the cursor on the screen. Also, it has the
Trackball Trackball function such as searching for images etc. in Cine
image.
Adjusts TGC value by depth by using 8 slides.

TGC Slide
TGC stands for Time Gain Compensation.
．．．．．．．
CAUTION
• If Gain value difference of adjacent TGC Slide is adjusted greatly, lines may occur on
images.
 Key Board
This is used to enter text etc.
[Figure 2.6 keyboard]
▐ Touch-Screen
This is the operation tool that users touch directly. The function that can be used in the
mode you are currently using appears in the form of button or dial button.

Service Manual
■ Screen configuration of touch screen

① Information area: The title of touch screen being currently used is displayed.
② Tab area: Diagnostic mode, Utility etc. are classified and displayed. You can
change the screen of touch screen by pressing tab.
③ Menu area: Menus that can be used in the current input mode are played in the
form of buttons. You can use it by directly pressing buttons and the menu being
used is displayed in orange.
④ Soft menu area: Soft menus that can be used in the current input mode are
displayed. The menu being used is displayed in orange frame.
Use it by pressing dial-button which is right below the menu or rotating it from
side to side.
※ Tip! If there are two touch-screen menus
If two menus appear at top and bottom, you can select the menu you want
by pressing the dial-button. Or press the button of menu you want to use on
the touch screen and then use dial-button.
① ②
④
[Figure 2.7 Touch Screen]
▐ Control of control panel
．．．．．．．
CAUTION
• Do not move control panel forcefully.
• Use the handle on the back of console when moving the product.

 Horizontal control
Hold the handle of control panel and move it from side to side carefully.
 Vertical control
Move the product up and down carefully pressing the lever on the handle of control
panel.

Service Manual
2.2.3 Console
Console is largely divided into two parts, inside and outside. The interior of the product is
mainly composed of devices responsible for the implementation of ultrasound imaging.
The exterior is composed of various connecting devices, probe holder, storage space,
handle, wheel etc.
▐ Rear Panel
It is located at the rear of the product and connected to various peripherals such as
monitor etc.
① Audio port (Output): Used in output of

audio signal
② Microphone port (Input):
Connects microphone.
③ Trig port (In/Out): not used.
① ④ DVI port (Output): prints out digital

signal to monitor.
[Figure 2.8 Rear panel]
．．．．
NO T E
• If connecting monitor to DVI port by using gender, we recommend connecting Full HD
wide monitor. If connecting general monitor such as analog RGB etc., the screen may
not be output correctly.

▐ Power connecting part
Located under the rear panel
①
③
②
[Figure 2.9 Power connecting part]
① Power switch: supplies or blocks power to the whole product
② Power Inlet: is connecting part of power cord connected to external
power.
③ Power input: is the part receiving power from power device inside the
product.
▐ Probe Holder
Holders to store Probe are mounted on the left and right of control panel.

Service Manual
2.2.4 Peripheral Devices

．．．．．．．
CAUTION
• Do not install peripheral devices not specified in this manual in the Patient
Environment. If installing other devices in the Patient Environment, electrical risk may
occur.
[Figure 2.10 Patient environment]
．．．．
NO T E
• For information on how to use peripheral devices, see the instruction manuals of the
product
▐ Internal peripheral devices

These are peripheral devices mounted inside the console. .
 DVD-Multi
DVD-RW, DVD+RW, DVD-R, DVD+R, CD-R, CD-RW, CD-ROM
 Hard Disc Drive
More than minimum 500Gbytes

▐ External peripheral devices
They are connected and used depending on your needs and mainly connected through
the port on the rear panel.
．．．．．．．
CAUTION
• In case of peripheral devices using USB port, be sure to turn off power before installing
or removing equipment to console. In the state that power is not turned off completely,
malfunction of peripheral devices for USB and system may occur.
．．．．
NO T E
• If trying to remove the removable disk, use Utility > Storage Manager.
• USB port of console is located in both front panel and rear panel of console. It is
convenient to connect saving device for USB (Flash Memory Media etc.) to port on the
front panel and other peripheral devices for USB to the rear panel.
The following products are recommended.
 USB Video printer

- BW : Mitsubishi P-95DE, Sony UP-D897
- Color : Mitsubishi CP-30DW, Sony UP-D25MD
．．．．．．．
CAUTION
• Be sure to install English Microsoft Windows XPTM compatible printer and driver. For
printer driver installation, contact the service department of Samsung Medison Co., Ltd.
• When connecting the printer, check if it is the same as the printer set in Microsoft
TM
Windows or Setup.
• Note that connected port is different depending on printer. General printer is connected
only to printer port and printer for USB only to USB port.
 USB RS-232C Serial cable

USB to Serial(RS-232C) Converter using FTDI Chipset(FTDI FT232BM
Compatible)
．．．．
NO T E
• For Open Line Transfer related contents, see ‘Chapter 5 Measurement’

Service Manual
 Foot Switch
It sets Foot Switch function in Utility > Setup > Peripherals > Foot Switch.
You can choose from Freeze, Update, Record, Print1, Save, Store Clip, Volume Start.
 Others
Flash Memory Media
．．．．
NO T E
• If using USB 1.1 Flash Memory, the system may not recognize the device. If this
situation occurs, Remove Flash Memory from the system and then install it again.
• In case of Flash Memory supporting the function other than general data storage
purpose, use it after checking if data storage function is working properly in desktop
PC.

2.2.5 Probe
Probe is the device obtaining data for ultrasonic Imaging by generating ultrasound
waves.
．．．．
NO T E
• For more details, see ‘Chapter 9 Probe’.
▐ How to connect probe

The work removing or attaching probe to probe connector should be performed in the
state of power-off for safety of the product and probe.
1. Connect probe to probe connector at the front of console. Up to 4 probes (5 including
CW) can be connected. But, connect CW probe to dedicated connector.
2. Install it by turning connector turning knob clockwise.
[Figure 2.11 Probe connector]

Service Manual
2.2.6 Accessory
This product provides the box containing various accessories.
[Figure 2.12 Accessory]
2.2.7 Option
This product has the following optional items.
4D Auto IMT
3D XI Elasto Scan
CW Function Panoramic
Cardiac Measurement 3DMXI Upgrade
DICOM HDVI
Spatial Compound Volume NT
XI STIC ADVR
For more information on the above options, see the contents of this manual.

2.3 Product specification
Height: 1,415 – 1,760mm (with monitor)

Physical Width: 549mm
Dimensions Depth: 1,002-1,137mm
Weight: 111kg (with monitor)
2D-Mode
M-Mode
Color Doppler
Pulsed Wave (PW) Spectral Doppler
Continuous Wave (CW) Doppler
Tissue Doppler Imaging (TDI)
Imaging modes Tissue Doppler Wave (TDW)
Power Doppler (PD)
Directional Power Doppler (DPD)
Color M-Mode
Anatomical Mode
3D imaging Mode
4D imaging Mode
Gray Scale 256 (8 bits)
Transmit focusing, maximum of eight points

Focusing (four points simultaneously selectable)
Digital dynamic receive focusing (continuous)
Linear Array
L4-7, L5-13IS, L7-16IS
Curved Array
C1-4, C2-6IC, C5-8, EC4-9IS, VR 5-9
Phased Array
Probes
P2-4BA
3D
V2-6, V4-8, V5-9
CW
CW 2.0, CW 4.0, CW6.0
Probe
5 Active Probe Ports (include pencil probe)
connections

Service Manual
Monitor 21.5 inch LCD monitor
ECG Type BF
Audio in / out
Microphone
Rear Panel External Trigger in / out
Input / Output External monitor DVI-I
Connections Network
USB
Foot switch
Maximum 12700 frames for CINE memory

Image Storage Maximum 8192 Lines for LOOP memory
Image filing system
Obstetrics, Gynecology, Urology, Abdomen, Cardiac, Vascular,

Application
Small Part, Pediatric, TCD, MSK, Contrast
Electrical Parameters 100-240V~, 1100VA, 50/60Hz
OB, Gynecology, Cardiac, Vascular, Fetal Heart, Urology,

Measurement
Abdomen, Small Parts, Muskuloskeletal, TCD, Pediatric Hips
Packages
* Refer the Chapter 5 for additional information
TGC control
Mode-independent gain control
Acoustic power control (adjustable)
Signal processing Dynamic aperture
(Pre-processing) Dynamic apodization
Dynamic range control (adjustable)
Image view area control
M-mode sweep speed control
Frame average
Edge Enhancement / Blurring
Signal processing Gamma-scale windowing
(Post-processing) Image orientation (left/right and up/down, rotation)
White on black/black on white
Zoom

Trackball operation of multiple cursors
2D mode: Linear measurements and area measurements
Measurement using elliptical approximation or trace
M mode: Continuous readout of distance, time, and slope rate
Doppler mode: Velocity and trace
USB Video Printer

USB to RS-232 Serial Cable
Foot Switch(IPX1)
Auxiliary
USB Flash Memory Media
USB HDD
Monitor
User Interface English, German, French, Spanish, Italian, Russian, Chinese
Operating: 700hPa to 1060hPa

Pressure Limits
Storage: 700hPa to 1060hPa
Operating: 30% to 75%

Humidity Limits
Storage & Shipping: 20% to 90%
O O
Operating: 10 C ~ 35 C
O O
Temperature Limits Storage & Shipping: -25 C ~ 60 C

Chapter 3
Product installation
Service Manual
Chapter 3 Product installation
3.1 Overview
Chapter 3 describes information needed to plan installation of A30 and install it. To install
the product in the best condition, it provides information about the transport and
installation environment. It included the process for installing the product and setting
method and explains the contents to check electrical safety. Also, the method
connecting probe and external peripheral devices is also included.
Contents
3.1 Overview .................................................................................................................. 3-1

3.2 Transportation .......................................................................................................... 3-3
3.2.1 Precautions for transportation ............................................................... 3-3
3.2.2 Humidity and temperature ..................................................................... 3-3
3.2.3 How to transport ...................................................................................... 3-3
3.3 Unpacking .............................................................................................................. 3-4
3.3.1 Dismantling of the product box .............................................................. 3-4
3.3.2 Checking product components ............................................................... 3-5
3.4 Installation conditions ............................................................................................ 3-6
3.4.1 Precautions................................................................................................ 3-6
3.4.2 Installation place ....................................................................................... 3-6
3.5 How to Install .......................................................................................................... 3-7
3.5.1 Installation Safety .................................................................................... 3-7
3.5.2 Connecting power cable .......................................................................... 3-8
3.5.3 Connecting network cable ..................................................................... 3-9
3.5.4 Connecting Foot switch .......................................................................... 3-9
3.5.5 Connecting probe ................................................................................. 3-10
3.6 Turning on the product ........................................................................................ 3-11
3.7 Product close ....................................................................................................... 3-12
3.7.1 Power switch ........................................................................................... 3-12
3.7.2 Power circuit breaker.............................................................................. 3-12
3.8 Connecting peripherals ....................................................................................... 3-13
3.8.1 Internal peripherals ............................................................................... 3-13
3.8.2 External peripherals .............................................................................. 3-13
Chapter3 Product installation 3-1

3.9 Setup....................................................................................................................... 3-15
3.10 System General Setup ......................................................................................... 3-16
3.11 Screen Setup (Display)......................................................................................... 3-19
3.12 Annotate ................................................................................................................. 3-22
3.13 Peripherals Setup .................................................................................................. 3-27
3.14 User Defined Key .................................................................................................. 3-30
3.15 Miscellaneous ........................................................................................................ 3-38
3.16 Option Setup (Option) ........................................................................................... 3-43
3.17 DICOM Setup (Option) ......................................................................................... 3-45
3.18 Auto Calc ................................................................................................................ 3-59
3.19 System information ............................................................................................... 3-61
3.20 Utility ....................................................................................................................... 3-84
Chapter 3 Product installation 3-2

Service Manual
3.2 Transportation
A30 is a finely tuned electronic medical device so careful attention is required while
transporting.
3.2.1 Precautions for transportation

1) Box packaging is designed to reduce the impact. However, be careful that external
shocks are not delivered to the product.
2) If the shock sensor below is on when shock is applied to the box or the box falls down,
contact global service group of Samsung Medison Co., Ltd or an authorized engineer
immediately.
．．．．
NO T E
• If direct shock is applied to the shock sensor, errors may occur.
[Figure 3-1] Shock sensor (attached to outside of the product box)
3.2.2 Humidity and temperature

“[Table 3-1] Humidity and temperature of the product” below represents the range
of temperature and humidity while transporting, storing, operating the product.
Classification Temperature [OC] Humidity [%]
Transport -25 ~ 60 20 ~ 90
Storage -10 ~ 50 20 ~ 90
Operation 10 ~ 35 30 ~ 75
[Table 3-1] Humidity and temperature of the product
3.2.3 How to transport
1) When moving or unloading the box in which the product is packed, we recommend

you to use a forklift or work with more than 4 people.
2) The product should be packed in the box and carried to the deliver place not to be
exposed to external shocks.

Service Manual
3.3 Unpacking Photo replacement
3.3.1 Dismantling of the product box

1) Remove strings fixing the box.
2) Separate the box top by lifting it up.
3) Separate the body of the box into both sides.
4) Strip the protective vinyl.
5) Take out probe box and component box and keep them in a safe place.
6) Unlock wheel locking
7) Grasp the back handle and pull it slowly to move to the installation place.
8) When moving on wheels, we recommend for more than 2 people to work. When
moving
[Figure 3-2] Dismantling of the product box

．．．．．．．
CAUTION
• It can cause serious injury when moving the product to distant places with a
large inclination angle,
3.3.2 Checking product components

Unpack the product and check product components. If different from purchased
components, contact a selling agency.
[Figure 3-3] Components

Service Manual
3.4 Installation conditions
3.4.1 Precautions
Manage the product by considering the followings.
1) Avoid watery places.
2) Keep the product out of the direct rays of the sun.
3) Avoid places showing drastic temperature fluctuations.
O O
4) For normal operation, 10 C ~ 35 C of temperature and 30% ~ 75% of humidity
should be maintained.
5) Avoid installing the product in places where heating appliances are close.
6) Avoid dusty or poorly ventilated places.
7) Avoid places with frequent vibrations.
8) Avoid places where there are chemicals or gases.
．．．．．．．
CAUTION
• If using the product near generators, X-rays equipment, transmission lines of a
broadcasting station, abnormal screen due to noise may occur.
• Also, using the same power with other electric appliances can cause noise.

3.4.2 Installation place
1) For the product to pass, the width of the door should be at least more than 70cm.
2) The distance between the back side of the product and the wall should be at least
more than 30cm.
3) Electric outlet and earth terminal, Lan connector (Ethernet Connector) should be
within 1 m with the product.
4) The lighting should be able to be adjusted lighter or darker.
5) There should be vents for air circulation.
[Figure 3-4] Installation place

Service Manual
3.5 How to Install
3.5.1 Installation Safety

．．．．．．
DANGER
broadcasting station, abnormal screen due to noise may occur.
• Also, using the same power with other electric appliances can cause noise.
[Figure 3-5] Connection of equipotential terminal (earth)

．．．．．．．
CAUTION
• When transporting or storing the product for a long time, check temperature and
humidity of the environment.
• Turn on power of the product by referring to the following “[Table 3-2] Temperature for
product use
• Sudden temperature change may cause product defect due to dew condensation etc.
Temperature -20 -15 -10 -5 0 5 10 ~ 35 45 50 55 60
Waiting time Usable

16 10 8 6 4 2 2 4 6 10
immediately
[Table 3-2] Temperature for product use

3.5.2 Connecting power cable
Be sure to measure power outlet output voltage of the installation place.
For stable power use of A30, use it within the following “[Table 3-3] Voltage for product
use” range. Connect power cable to the back side of A30.
．．．．
NO T E
• The product may be shipped with the product and power cable connected.
[Figure 3-6] Power of the product
voltage Voltage error range Current Frequency
100-120VAC +/- 10% 10A 50~60Hz
200-240VAC +/- 10% 10A 50~60Hz
[Table 3-3] Voltage for product use

Service Manual
3.5.3 Connecting network cable – photo correction

Connect network cable to the back side of ACCUVIX XG.
[Figure 3-7] Connecting network cable

3.5.4 Connecting Foot switch – Photo correction
Connect Foot Switch to USB port on the back side of ACCUVIX XG.
[Figure 3-8] Connecting foot switch cable

Service Manual
3.5.5 Connecting probe

There are 4 probe connections on the front side of ACCUVIX XG. Probe connection
names are No. 1, No. 2, No.3 from the left and can be connected regardless of the type
of probe of ACCUVIX XG. Put probe in probe holder and start connector connection.
．．．．．．．
CAUTION
• To prevent damage of connector PCB and connecting pin of probe, do not apply
excessive force when connecting.
1) Connect in the state that probe handle is unlocked (state rotated in the
counterclockwise direction).
2) Connect it to connection with probe cable pointing down
3) Rotate probe handle clockwise and fix it to the opposite position of cable
[Figure 3-9] Probe connection

．．．．．．．
CAUTION
• Even when power is on, probe can be connected freely but do not connect or separate
probe while booting the product.

3.6 Turning on the product Photo correction
1) Check if power capacity of A30 is suitable once again and connect power plug to
power outlet.
2) Check if power cable and A30 is connected correctly and turn on the switch of power
circuit breaker [Figure 3-10].
Circuit
breaker
[Figure 3-10] AC power

．．．．．．．
CAUTION
• Turn on AC power on the back of the product and then turn on the power of the
product after approximately 10 seconds.
• While booting, do not press the button of Alpha-numeric keyboard or make sure that
the button is not pressed. It may cause system malfunction.
• If turning on power of the product in the state of turning it off forcefully, the system may
be turned on instantly and then off. This is the characteristic of Intel® PC Main Board
built in the product and not the error of the system.

Service Manual
3) If pressing On/Off switch on the left of control panel (keyboard) of A30, it starts
operating.
[Figure 3-11] Power switch
① The booting process is checked on LCD monitor and as Window XP logo

disappears, A30 logo and loading bar appear.
② The loading bar is filled with a color and this time shows the process that the
software moves data into Front End Part and Back End Part of the system.
③ If the software data moving process is done, 2D screen appears and A30 is ready
for use.

3.7 Shutting down product
To shut down A30, use power switch and power circuit breaker.
3.7.1 Power switch

Press the power switch button on the left of control panel (keyboard) as long as 2
seconds.

．．．．．．．
CAUTION
• [On/Off] If pressing the button long for more than 5 seconds, the power of the product
is turned off forcefully but it may cause damage to hard disk of the product.
• If the symptom is persistent, contact global service group of Samsung Medison Co.,
Ltd or an authorized engineer
3.7.2 Power circuit breaker

1) This is the method to block power applied to the product after turning off the product with
power switch.
2) Turn off power circuit breaker if not using the product for a long time or repairing the
product.
Circuit
breaker

Service Manual
3.8 Connecting peripherals

To connect with external devices, A30 is composed of several kinds.
The representative external devices are black and white printer, color printer, line printer,
USB storage device, VCR etc. You can use by connecting them depending on your
needs and usually connect them through the port on the rear panel.
．．．．
NO T E
• For information on use of peripheral devices, see the user’s manual of the product.
3.8.1 Internal peripherals

These are peripheral devices mounted in the interior of the console.
3.8.1.1 DVD-Multi
DVD-RW, DVD-RAM, DVD-R, DVD+R, DVD-ROM, CD-R, CD-RW, CD-ROM
3.8.1.2 Hard Disc Drive
500Gbytes.
3.8.2 External peripherals

You can use by connecting them depending on your needs and usually connect them
through the port on the rear panel.
．．．．．．．
CAUTION
• In case of peripheral devices using USB port, be sure to turn off power before
mounting devices on the console or remove them.
• If power is not turned off completely, malfunction of peripheral devices for USB and
system may occur.
．．．．
NO T E
• To remove the removable disk, use Utility > Storage Manager.
• USB port of console is located on both front panel and rear panel of console.
• It is convenient to connect saving devices for USB (MO drive, Flash memory media
etc.) to the port of the front panel and other peripheral

3.8.2.1 Video Cassette Recorder (VCR)
Panasonic MD835, SONY DVO-1000MD, JVC BD-X201, Mitsubishi MD3000
3.8.2.2 Video Video Page printer

Color : Mitsubishi CP910U, Mitsubishi CP910E, SONY UP-20
Black and White : Mitsubishi P93WM, SONY UP-897MD
3.8.2.3 USB Video printer

Color : Mitsubishi CP-30DW, Mitsubishi CP-900DW, SONY UP-D21MD, SONY UP-
D23MD
Black and White : Mitsubishi P93DW, SONY UP-D897
．．．．．．．
CAUTION
• Be sure to install English Microsoft Windows XPTM compatible printer and driver. For
information on installing printer driver, contact Samsung Medison Co., Ltd Global
service group.
• When connecting a printer, check if it is the same as the printer set in Setup or
Microsoft Windows TM.
• Note that connecting port is different depending on your printer. General printer should
be connected to the printer port and printer for USB to USB port.
3.8.2.4 USB RS-232C serial cable

USB to Serial(RS-232C) Converter using FTDI Chipset (FTDI FT232BM Compatible)
3.8.2.5 Miscellaneous
Flash Memory media
．．．．
NO T E
• If using USB 1.1 Flash Memory, the system may not be able to recognize the device. If
this situation happens, remove Flash Memory from the system and then install it again.
• In case of Flash Memory supporting the function other than general data saving, use it
after checking if data saving function operates properly in desktop PC.

Service Manual
3.9 Setup
This is the description on various settings of the system not affecting images. It can be
changed depending on your needs and tastes.
1. Press [Utility] > [Setup] on the touch screen.
2. Setting screen appears on monitor and touch screen. Select the tab where
the item to be set belong.
※ Tips! – How to select tab
You can select the tab you want with the following two methods.
Select the method that suits your preferences.
- Select the tab of the monitor screen by using trackball and [Set] butt
on.
- Press the button on touch screen.
3. Set for each item.
4. Save setting and then close.
5. If pressing [Close] of monitor screen or [Exit] of touch screen, [Exit] button ofcontrol
panel, it is switched to scan mode. If pressing [Return] of touch
screen, it goes back to Utility screen, the previous step.
[Figure 7.1 Setup- touch screen]

3.10 System General Setup
Select [General] tab in Setup screen. Or press [General] of touch screen.
Conduct system general setup such as title etc.
[Figure 7.2 Setup-General]
3.10.1 Title
The contents displayed in the title area of the screen are set.
3.10.1.1 Institution
The name of hospital/institution where the product is installed is entered.
．．．．
NO T E
• The following special characters cannot be entered; #, [, ", :, ?, |, \, "
3.10.1.2 Department
Detailed information of hospital/institution is entered. Entered contents are used to
classify information when transmitting DICOM.

Service Manual
3.10.1.3 Date
The current date is displayed. Press to change the date.
．．．．
NO T E
• You cannot change the date and time in the state that patient ID is registered. End the
current diagnosis by pressing [End Exam] of control panel and then change.
• Year can be set between 2006 ~ 2007.
※Tip! How to set date (or time)
1. Press in Date (or Time).

2. Set date and time by using [Set] button and trackball of control panel.
3. If setting was done properly, press [Apply] to apply setting and then press
[Ok] to close date and time setting window.
4. To cancel setting, press [Cancel] or [Exit] button on control panel.
[Figure 7.3 Date & Time]
3.10.1.4 Date Format

Set date display format. Press combo button to select the display format you
want.Set date display method is applied to various date enter boxes of Patient
Information.
3.10.1.5 Time
The current time is displayed.

3.10.1.6 Time Format
Time display format is set. Press combo button to select desired display format
(12 Hour, 24 Hour).
3.10.2 Store Clip
3.10.2.1 Store Clip Method

Set storing method and scope by acquiring images. You can select one from ECG Beat,
Time, Manual. But, ECG Beat can be selected only when ECG is On.
- ECG Beat: Sets the number of heartbeat and can be set up to 1~8 Beat.
- Time: Is set in second unit and can have 1~50 seconds (sec) of value.
- Manual: After pressing the button designated as [Store Clip], the images up to 50
seconds is automatically saved.
3.10.2.2 Cine Loop Period

- Prospective: When pressing the button designated as [Store Clip] of control panel
while scanning, the image after pressing the button is saved.
- Retrospective: When pressing the button designated as [Store Clip] of control panel
while scanning, the image before pressing the button is saved.
．．．．
NO T E
• [Store Clip] button is set in Utility > Setup > User Defined Key > User Key 2, 3
3.10.3 Control
3.10.3.1 Trackball Speed for Scan Mode

It sets the speed of trackball in scan mode (Slow, Normal, Fast).
3.10.3.2 Trackball Speed for Measurement

It sets trackball speed when measuring (Slow, Normal, Fast). Slow movement of
trackball is useful for detailed measurement.

Service Manual
3.10.4 Scan Mode
3.10.4.1 Simultaneous Mode

It is the function determining whether to activate simultaneous mode in spectral Doppler
mode.
- Off: Selected if not using simultaneous mode
- Allow B/PW: Selected if only using simultaneous mode of 2D/PW, not using
simultaneous mode of 2D/C/PW
- Allow B/C/PW: Selected if using both simultaneous mode of 2D/PW and simultaneous
mode of 2D/C/PW.
3.10.4.2 Dual Mode

It sets if Change Window is activated in dual mode.
3.10.4.3 Dual Live

The position of color Doppler mode is selected in Dual Live mode.
- Left / Top: Color Doppler mode is located in left or top.
- Right / Bottom: Color Doppler mode is located in right or bottom.
- Dual Live Left-Right Dual Only: If selecting check box, Top-Bottom Dual button
disappears.
3.10.4.4. Freeze Action

When pressing [Freeze] button of control panel, the function to run is automatically
selected. One of None, Body Marker, Caliper, Measure is selected..
3.10.4.5 End Exam Action

- End Exam Only: If pressing [End Exam] button of control panel, Exam is finished and
the screen is switched to B mode Scan.
- End Exam + Patient: If pressing [End Exam] button of control panel, the screen is
switched to Patient Information screen.
3.10.4.6 Option
You can select multiple items. You can check or lift checking by selecting an item with
trackball and [Set] button.
- Auto Freeze: Scan mode is automatically stopped after 10 minutes without using the
product.

※Tip!
Scan mode is stopped regardless of selecting Auto Freeze after 1 hour without
using the product.
．．．．
NO T E
• In Live 3D mode, it is set to operate Auto Freeze function in 20 minutes.
- HPRF: It sets use of HPRF(High Pulse Repetition Frequency) supported in PW

spectral Doppler mode. If selecting the check box, HPRF function is supported.
- Color Map Auto invert: If selecting the check box, Color Map map is automatically
inverted. It is only applied when changing Steer in DPDI mode among 2D/C/D mode
and C mode, PD mode.
- M/PW Loop Side by Side: It adds Loop Side by Side display method in M mode or
power spectral Doppler mode.
- Width Rescale: When adjusting Depth in 2D image, it automatically adjusts the size of
images to fit the screen size. But, it is only available in Linear probe.

Service Manual
3.11 Screen Display Setup(Display)

Select [Display] tab in Setup screen. Or press [Display] of touch screen.
Information related to image display is set.
[Figure 7.4 Setup -Display]
3.11.1 Display
3.11.1.1 Option
You can select multiple items. Select an item and check it or lift the mark by using
- Name + Age: It sets whether to display name and age under patient ID.
- Name + Birthday: It sets whether to display name and birthday under patient ID.
．．．．
NO T E
• ‘Name + Age’ and ‘Name + Birthday’ cannot be used at the same time.
- TGC Line: It sets whether to display TGC Line. When setting TGC line in TGC Line off,
TGC line appears and disappears after 3 seconds.
- Image Info: It sets whether to display image information. If turning off this function
when image information covers images, image information is not shown.
- Display Blank: It sets whether to display screen saver. If it is ‘On’, the time thatscreen
saver is activated can be set between 1~30 minutes.
- TI (Thermal Index) Display: It sets TI appearing on the screen as one among TIs(Soft

tissue thermal Index), TIb(Bone thermal index), TIc(Cranial bone thermal index.
3.11.1.2 Doppler Axis

It selects the scale unit of Axis in spectral Doppler mode.
- Velocity: Expresses the scale unit of Doppler Axis as m/s(or cm/s).
- Frequency: Expresses the scale unit of Doppler Axis as kHz.
3.11.1.3 LMP / GA / EDD Display

It sets how LMP, GA, EDD entered in Patient Information screen are displayed inthe
monitor screen. Select two among LMP, GA, EDD.
- Information Bar (Replace ID): Is displayed in ID position of title area
- Information Bar (Replace Name): Is displayed in patient name position of title area.
- Information Bar (Replace App.): Is displayed in diagnostic subject position of title area
- Measure Result: Is displayed with measurement results when measuring.
- None: Nothing is displayed on the screen.
3.11.2 Font
3.11.2.1 Font
You can set the object for which font you try to set will be used. Select between
Document Font and Measure Result Font.
3.11.2.2 Font Name

You can set the font of characters.
3.11.2.3 Font Size

You can set the size of characters.
3.11.2.4 Font Color

You can set the color of characters.
3.11.2.5 Preview

Service Manual
You can preview set font.
3.11.2.6 Default
You can set as default character setting of the system. The basic setup is as follows.
Document Font Measure Result Font
Font Name Helvetica Verdana
Font Size 11 11
Font Color White Yellow
．．．．
NO T E
• In case of particular font, characters may not display correctly on the screen.

3.12 Annotate
Select [Annotate] tab in Setup screen. Or press [Annotate] of touch screen.
Set information related to image input.
[Figure 7.5 Setup –Annotate]
3.12.1 Screen Keyboard

Screen Keyboard
You can directly enter patient information by using screen keyboard in Patient
Information screen. If setting to ‘On’, Screen Keyboard function is supported.
．．．．
NO T E
• When entering birthday and age, Screen Keyboard with which you can enter numbers
is activated.
3.12.2 Body Marker
3.12.2.1 Size
You can set the size of Body Marker figure (Small, Medium, Large).
3.12.2.2 Option
Body Marker Auto Active: You can set whether to activate Body Marker mode
automatically when changing active image area.

Service Manual
3.12.2.3 Body Marker Edit
[Figure 7.6 Body Marker Edit]

① Body Marker list: Contents differ depending on group selected in ‘Group’. ‘Current
page/ number of total pages’ is displayed under list. If there are more than 2 pages,
change page by using [⇨] or [⇦].
② Body Marker list of preset and probe currently being used: ‘Current page/number of
total pages’ is displayed under list. If there are more than 2 pages, change page by
using [⇨] or [⇦].
．．．．
NO T E
• Each list can save 1~ 100 Body Markers.
- Add Body Marker

- Select Body Marker in the left list (①) and then double-click it. Selected Body Marker is
added to the right list (②). You cannot add already existing Body Marker and a
message appears.
- Remove Body Marker
- Select Body Marker in the right list (②) and then double-click it.
- Add and cancel Body Marker list
- Press [Save] to save list. Press [Close] to cancel.
- Initialize Body Marker list
- Press [Reset]. It is returned to the system original setting.

3.12.2.4 Text Setup
You can set whether to use Quick Text, Auto Text Erase, Boot up Caps Lock on, Auto
text, Edit Text, Auto text Edit, Clear Annotation etc.
 Quick Text
If selecting the checkbox, you can use Quick Text function.
Quick Test is the function of making the mode converted to text input mode immediately
when pressing character key of Alpha Numeric Keyboard,
．．．．
NO T E
• Quick Text checkbox is selected as the default of the system.
• You can input text even when use of Quick Text function is not set. In this case,
to switch to text mode, When selecting Annotation in touch screen, it is entered into
text mode.
 Auto Text Erase

If selecting the checkbox, when returning to scan mode by pressing [Freeze] button after
entered text, all entered texts are automatically deleted.
 Boot up Caps Lock on
If selecting the checkbox, Boot up Caps Lock on function is on. When entering text, it is
entered as alphabet capital letters.
 Auto text
If entering Abbreviation, the system automatically looks up Full word and enters it. If
using this function when entering text, you can enter text quickly and easily.
For example, if entering the text, ‘Abdominal Circumference’, if a user only enters ‘AC’,
the system automatically looks up Full word and displays it on the screen. If trying to use
Auto text function, select [Auto text] checkbox by using trackball.
If trying not to use it, lift the check of the checkbox.
If setting to use Auto text function, Abbreviation list appears on the screen when entering
text.
[Figure 7.7 Abbreviation list]
In the system, Abbreviation list for this function is saved. You can use Abbreviation list by
adding and editing it according to your preference.

Service Manual
※ Setting Abbreviation list
Press [Auto text Edit] button to set Abbreviation list saved in the system. It is
switched to Auto text Edit screen. Press [Close] button to save Abbreviation
list and exit setting.
- Modifying words
1. Select words you want to modify in the list by using trackball and [Set]
button. Abbreviation of selected words and their Full words are displayed
in Abbreviation and Full Word box under the screen.
2. Modify words in Abbreviation and Full Word box. Abbreviation list is
modified in real time.
- Add word
1. Press [New] button.
Enter words you want to add in Abbreviation and Full Word box under the
screen. Words are added to Abbreviation list.
- Delete word
1. Select words you want to delete in the list by using trackball and [Set]
button. Abbreviation of selected words and their Full words are displayed
in Abbreviation and Full Word box under the screen.
2. If pressing [Delete] button, warning message appears
3. Press [Ok] to continue and delete selected words. Words are deleted in
Abbreviation list. Press [Cancel] not to delete.
- Setting word input delay time

When entering text, you can set time required that Abbreviation
is automatically switched and entered
Set input delay time in Auto text Delay Time box under the screen in 0.1 ~
5 second unit.

[Figure 7.8 Auto text Edit]
 Clear Annotation
If selecting check box, Annotation entered when changing mode is deleted.
 Edit Text
A full text page is edited by selecting Application that you want to change.
[Figure 7.9 Edit Text]

Service Manual
3.13 Peripherals Setup

Select [Peripherals] tab in Setup screen. Or press [Peripherals] of touch screen. Set
button, key and peripherals connected to the product.
[Figure 7.10 Setup -Peripherals]
3.13.1 Peripherals
3.13.1.1 VCR Model

It is set as Built-in Recorder. You cannot change setup.
3.13.1.2 COM
You can set devices to be connected to the serial port. You can select one from Open
Line Transfer or Reserved. If selecting Reserved, COM is not available.
To complete connection of devices after selecting Open Line Transfer, you must reboot
the system.

3.13.2 Foot Switch
You can set the function of left and right pedal of Foot Switch. The functions that can be
set are as follows.
Freeze, Update, Record, Print 1, Save, Store Clip, Volume Start.
3.13.3 Print Setup
3.13.3.1 Printer Orientation
．．．．
NO T E
• It can be set only in case of eco printer using roll paper.
You can set the type and printer orientation of eco printer.
- Printer setup: selects printer to be used by using combo button.
- Portrait: prints vertically long.
- Landscape: prints horizontally long.
3.13.3.2 Print Key

You can set the type of printer to be used when pressing [Print 1] and [Print 2] button of
control panel.
3.13.3.3 Measure Report print

You can set printer to print measure report in A4/ Letter form by selecting the checkbox.
3.13.3.4 Local Printing Area

You can set print area.
- Video Out (1280 x 872): Prints only part of screen (1280 x 872) including image area
- Image Only: prints only image area.
3.13.3.5 Printing Image Adjustment

You can adjust print quality of image. Select the type of image and printer and then,
adjust Gamma, Brightness, Contrast.

Service Manual
．．．．
NO T E
• This function is supported only in some Digital Printers.

3.14 User Defined Key
Select [User defined Key] tab in Setup screen. Or press [User Defined Key] of touch
screen. Set keys, buttons connected to the product.
[Figure 7.11 Setup –User Defined key]
3.14.1 Set / Exit Key Switch
3.14.1.1 Set / Exit Key Switch

You can set the function of buttons on the left and right of trackball of control panel.
- Set / Exit: Sets the left button as [Set], right as [Exit] function
- Exit / Set: Sets the left button as [Exit], right as [Set] function.
3.14.2 User Key Setup
3.14.2.1 User Key

You can set the function of [User 1] and [User 2], [User 3] button f control panel.
The functions that can be set are as follows.
User 1 None, Gain, Frequency, Power, Angle, EZ Exam
User 2 / None, TDI Mode, TDW Mode, Store Clip, Save, Record, Print 2, M
Line, Dual, Quad, Dual Live, Change Window, Probe Change,
User 3
Application Change, Biopsy, Annotation, Body Marker,
Simultaneous, EFW Measure, EFW Result, BPD, HC, AC, FL,
APTD, TTD, FTA, GS, CRL

Service Manual
3.14.3 Printer Key
3.14.3.1 Printer Key

- Print Only: prints only image.
- Print + Image Save: prints and save image.

3.15 Miscellaneous
Select [Miscellaneous] tab in Setup screen. Or press [Miscellaneous] of touch screen.
You can set E-mail and text, network state etc.
[Figure 7.12 Setup - Miscellaneous]
3.15.1 E-mail
You can set server to send/receive E-mail with this product.
3.15.1.1 Mail (SMTP) Server

Set E-mail server.
3.15.1.2 Port No
Enter port No.
3.15.1.3 ID
Enter access ID of E-mail server to be used.

Service Manual
3.15.1.4 Password
Enter access password of E-mail server to be used.
3.15.2 Buzzer Control

When button or dial-button is used, buzzer notifies you of whether to be used.
3.15.2.1 Buzzer Sound

Turn on or off by using trackball. It will sound every time you use button or dial-button.
3.15.3 MIC
While MIC is inserted to MIC Jack of Rear Panel, You should turn on the
MIC in Miscellaneous Mode . Otherwise, MIC should be not to be off.
3.15.3.1 MIC ON
- You can check whether MIC’s operation and Volume is normal or not Due to MIC
howling sound.
- MIC signal is outputted via VHS output.
- MIC signal is recorded in ADVR recording mode.
- While MIC mode is turned on without MIC, noise maybe can be mixed in external output
signal.
3.15.3.1 MIC OFF

- MIC signal is not outputted through Speaker.
- MIC signal is not outputted through VHS OUTPUT
- MIC signal is not recorded in ADVR recording mode.
- Noise is protected in external output signal.
3.15.4 Account
Set your ID register and Password.
3.15.4.1 User ID and Password

You can set your account function (Log-in) use. If Account is On, applicable cases are

as follow.
- Blank Image (Screen Saver)
- Sonoview / Patient entry
- Search window of Patient
3.15.4.2 Set ID and Password

It is administer only function and account is managed after approval. Account List
window is activated.
- Add: After filling out User ID, Password, Name box, press Add button to add new ID.
- Modify: saves modified matters.
- Delete: deletes selected ID.
- Close: closes setup.
3.15.4.3 Log in
After logging in with Admin account, you can set up user account ID.
For Admin account, please contact service engineer.
．．．．
NO T E
• Admin account cannot be deleted.
• If user account function is activated, another Exam cannot be loaded in the not logged
in state
• Password should be less than 6 ~15 characters and at least 3 of the following should
be combined
- English capital letter
- English small letter
- Number
- Special characters
3.15.4 Export Image Compensation

You can set Post Curve of images to use DICOM service. If pressing button,
Compensation window appears. Adjust Gamma, Brightness, Contrast by using each
slide. Press [Default] to Initialize to system default settings

Service Manual
※ Compensation
If adjusting Post Curve, it is convenient for diagnosis because when reviewing

images in other monitors, they are expressed as close to the original.
[Figure 7.13 Compensation]

3.15.5 Touch Screen Calibration
You can start Calibration of touch screen.
※How to calibrate touch screen
1. Press [Touch Screen Calibration]. Calibration window appears on touch screen.

2. Press flickering X mark on touch screen.
- If pressing for 3~4 seconds, the following X mark appears with a beep.
- Press total 25 of X marks in the same way.
3. If calibration is complete, the screen to save the current coordinates appears.
．．．．．．．
CAUTION
• Do not reboot or turn off while saving coordinates
4. If saving screen disappears, reboot equipment.
3.15.6 Patient Name Formatting

This is the function displaying patient names in languages used by Asian patients such
as Korea, China,Japan etc.
Press [Reset] to initiliaze setup.
．．．．
NO T E
• This button is shown in the screen only in the product applying Asian Patient function.
3.15.6.1 Name Formatting

You can set the order displaying the names of patients.
- Default: displays in the order of last name, first name, middle name (example; Smith,
Robert L).
- Custom: The order of last name, first name, middle name is specified in ‘item’ and sign
use such as comma, Space, Omit etc. is specified in ‘Separator’.
3.15.6.2 Representation Priority

Patient Information
The method representing the name of patients is set. Set the method which will be used
by priority among Roman, Ideographic, Phonetic according to 1, 2, 3.

Service Manual
3.16 Option Setup(Option)

Select [Option] tab in Setup screen. Or press [Option] of touch screen.
Set whether to use option software or hardware or lift setup.
[Figure 7.14 Setup -Option]

* The figure above may differ from the actual system options.
3.16.1 Options
The list of option software is displayed.
．．．．
NO T E
• Contact the retailer of the product to purchase option software.
3.16.1.1 Option
The kinds of option software that can be installed in this product are displayed.
3.16.1.2 Status
The current status of option software is displayed.
- Lock_Not Installed: Hardware is not connected.
- Lock_Unregistered: Use of software is not registered.
- Lock _Installed: Hardware installation is complete but cannot be used.
- Unlock_Permanent: State to be used without restriction in the use period.
- UnlLock_Restricted: State to be used during a certain use period.
- Lock_Expired: State that cannot be used after a certain use period in Restricted setting

state.
3.16.2 HW Configuration
The list of option hardware is displayed. Only current ECG is supported. Check the
check box of hardware to be used. To complete setup, reboot the system.

Service Manual
3.17 DICOM Setup(Option)

Select [DICOM] tab in Setup screen.
Or press [DICOM] of touch screen. Set DICOM (Digital Imaging and Communication in
Medicine) operation and DICOM server.
．．．．
NO T E
• For more information, see the instruction manual of the server and DICOM
Conformance Statement.
[Figure 7.15 Setup -DICOM]
3.17.1 DICOM Configuration

Information on DICOM server being used in this system is displayed. You can modify
information or add, delete server. Information on the server is used as information
to distinguish DICOM of this system and also used to transmit and receive data with
other DICOM servers.
．．．．
NO T E
• Set ‘IP Address’, ‘AE Title’, ‘Port No’ by contacting with Network representative of the
institutions where this product is installed.

AE Title
Input DICOM AE(Application Entity) name. It is used to distinguish devices
using DICOM in the network.
Station Name
You can enter the name of this system. In some cases, it is used to distinguish
in DICOM network with ‘AE Title’.
Port No
You can enter Port Number of the used server.
3.17.2 DICOM Send Format

You can set the saving type of 2D or color image to use DICOM service. Select one
between Color and Gray by using combo button. If selecting Gray, Only black and
white images are saved.
．．．．
NO T E
• Settings of DICOM Send Format are applied at the time of saving images.
• That is, if set as Gray, it is saved as black and white image when saving images.
3.17.3 DICOM Compression

You can set whether to compress still images to use DICOM service. Select between
Uncompressed and JPEG Baseline by using combo button. If selecting Uncompressed,
you can saving without compressing images
．．．．
NO T E
• Settings of DICOM Compression are applied at the time of saving images. That is, if
set as JPEG Baseline, images are compressed when saving images.
3.17.4 Store SR at End of Exam

You can select whether to store SR at End Exam. If selecting the checkbox, it is
automatically saved at End Exam and if not selecting, not saved.

Service Manual
3.17.5 Add DICOM Service

Press [Add] in the screen. Screen is converted to the one inputting DICOM service to be
added. Press [Save] to store input contents after adding service. Press [Cancel] to
cancel.
Servoces
You can select the types of services to be used through DICOM. DICOM servers that
can be set are Storage, Print, Worklist, PPS, SC, Storage SR.
Alias
You can input the name of DICOM server.
AE Title
You can input AE Title of DICOM server. Input by contacting with Network representative
of the institutions where this product is installed.
Transfer Mode
You can set transfer mode.
- Batch: When pressing [End Exam] button, saved images can be transferred at once.
- Send As You Go: Transfers images every time you save images by using [Save]
button.
- Manual: Specifies and transfers images at a user’s disposal at Exam List, SONOVIEW.
Connect Timeout
If there is no response from DICOM server during set time, connection is terminated.
Input in second unit (s).
IP Address
Input IP Address of the server used. Input by contacting with Network representative of
the institutions where this product is installed.
Port No
Input Port Number of the server used. Input by contacting with Network representative
of the institutions where this product is installed.
Retry Interval
In case of transfer failure, you can set after how many seconds you will retry
transfer. Input in second unit (s).
Maximum Retries
In case of transfer failure, you can set how many times you will retry transfer.

3.17.6 Storage server information
Select [Services] item as ‘STORAGE’. Set image storage service using DICOM.
3.17.6.1 Storage Options

- Send Cine Loops: You can transfer Cine Loops if selecting the checkbox.
- Include Pixel Spacing: In addition to area information used in ultrasonography, area
information used in CT or X-Ray test is additionally included. You can perform
measurement in PACS system not supporting ultrasonic area information.
．．．．
NO T E
• But, the types of images supported are 2D, 2D Color mode and for Dual, Quad mode,
Depth of included images should be the same.
- Include 3D Volume: When transferring 3D images, you can set whether to transfer
with 3D volume data
．．．．
NO T E
• Select only if using Storage service supporting 3D volume data of Samsung Medison
Co., Ltd.

Service Manual
3.17.6.2 VOI LUT Setup

Set VOI LUT(Value Of Interest Look Up Table). Save by adjusting Contrast and
Brightness of DICOM images. Saved images can be checked in PACS devices using
standard VOI LUT of DICOM.
- Window Center: Input the values to be set in DICOM Tag(0028,1050).
Set values mean Brightness of images displayed in Storage service.
Based on 128, the greater the set value, the darker.
But, you can use it only when Storage service supports this function.
- Window Width: Input the values to be set in DICOM Tag(0028,1051).
Set values mean Contrast of images displayed in Storage service.
Based on 256, the greater the set value is, the smaller contrast is.
You can use it only when Storage service supports this function.
[Figure 7.16 DICOM Configuration -Storage]
3.17.7 Print server information

[Services] item is selected as ‘PRINT’. Output service using DICOM is set.
．．．．
NO T E
• Only printers connected to DICOM network can be set.
• The following functions may not be available depending on the features supported
by the printer connected.
• Set printer service after looking at DICOM Conformance Statement or the instructions
manual of printer first.
Color
You can set whether to use color of the printer to be used. Select one between black
and white (Grayscale) and color (RGB).

Format
You can set layout of paper. Select one from 1ⅹ1, 1ⅹ2, 2ⅹ2, 2ⅹ3, 3ⅹ3, 3ⅹ4, 3ⅹ5,
4ⅹ4, 4ⅹ5, 4ⅹ6.
Orientation
You can set orientation of paper. Select one between horizontal (Landscape) and
vertical (Portrait).
Magnification
If resizing image to be printed, you can set Interpolation to be used. Select one from
Replicate, Bilinear, Cubic, None.
Border Density
You can set border color of image to be printed. Select one between Black and White.
Empty Density
You can set background color of the area to be printed Select one between Black and
White.
Min Density
You can set minimum brightness of image to be printed. If not inputting, it is replaced
with default set in the printer.
Max Density
You can set maximum brightness of image to be printed. If not inputting, it is replaced
with default set in the printer.
Medium Type
You can set the type of paper. Select one from paper, Clear Film, Blue Film, Mammo
Clear Film, Mammo Blue Film
Film Size
Set the size of paper. Select one from 8inchⅹ10 inch, 5 inchⅹ11 inch, 10 inchⅹ12 inch,
10 inchⅹ14 inch, 11 inchⅹ14 inch, 11 inchⅹ17 inch, 14 inchⅹ14 inch, 14 inchⅹ17
inch, 24cmⅹ24cm, 24cmⅹ30cm, A4, A3.
Destination
You can set way out where paper is output. Select one between Magazine and
Processor.
Smoothing Type
Used only when ‘Magnification’ is set as ‘CUBIC’. Input the value listed in DICOM
Conformance Statement of printer.
Priority
You can set processing priority for output order of printer. Select one from High, Med,
Low.

Service Manual
Copies
Input number of copies to be printed from 1 to 99
Configuration Info
You can set characteristic value of printer. See DICOM Conformance Statement of
printer.
[Figure 7.17 DICOM Configuration -Print]
3.17.8 Worklist server information

Select [Services] item as ‘WORKLIST’. Set Modality Worklist service using DICOM.
Show Worklist first when the patient screen opens

If selecting checkbox, Worklist window appears when pressing [Patient] of control panel.
If not selecting it, Study Information window appears.
Update Method
You can set update method of WorkList.
- Only on user Request: Updated only when user wants
※ Tip! If trying to update Worklist, select Search Source as [Worklist] in [Search]

tab of Patient Information screen and then, press [Search].
- On Startup and Every: When booting the system, after WorkList is updated, it
is updated automatically every set period of time.
Scheduled Station AE Title
You can set the range of AE Title to bring from Worklist server of a hospital.
- Any: Brings the patient list saved in all AE Titles in the server

- This System: Brings the patient list of AE Title set in DICOM tab.
- Another: A user brings the patient list by directly inputing particular AE Title.
．．．．
NO T E
• This function can be used only in the state that Worklist is set.
Start Date
You can set the range of date to be searched.
- Today: Brings the patient list of current date.
- Range: Brings the patient list from n date to n date based on the current date.
- Past Week: Brings all patient lists until a week ago based on the current date.
- Past Month: Brings all patient lists until a month ago based on the current date.
- Custom Date: Brings all patient lists of the date by specifying a particular date.
Study Description Priority
When loading Exam from Worklist server, you can set the priority of items to be
shown Patient Information > Patient > Description. The priority of the items on top of list
is the highest and as going downward, the priority gets lower. Select items that you want
to change the ranking and then, adjust position by pressing [Up], [Dn] button.

Service Manual
Modality Type
Set the kind of Modality when brining Exam from Worklist server.
- Any: Brings all Exams registered in Worklist regardless of Modality.
- US: Only brings Exam registered as UltraSound
- Another: Directly enters Modality that a user wants and only brings Exam
corresponding to entered Modality. If nothing is entered, it is the same as ‘Any’.
[Figure 7.18 DICOM Configuration -Worklist]
3.17.9 PPS server information

[Services] item is selected as ‘PPS’(Performed Procedure Step). You can set Modality
Performed Procedure Step service using DICOM.
Setting method is the same as Storage server.
[Figure 7.19 DICOM Configuration -PPS]

Always complete exams
If selecting the checkbox, Exam is always reported as the completed state.
If pressing [Cancel] button without selecting the checkbox, cancel message is
transferred to RIS server.
3.17.10 SC server information

Select [Services] item as ‘SC’(Storage Commitment). Set Storage Commitment service
using DICOM. Storage Commitment service is used after finishing diagnosis and
transferring all saved images and reports.
Associated Storage Server
Select image storage server to be connected.
[Figure 7.20 DICOM Configuration -SC]
3.17.11 Storage SR server information

Select [Services] item as ‘Storage SR’(Storage Structured Report). Set DICOM as used
report storage service.
Setting method is the same as Storage server.
[Figure 7.21 DICOM Configuration –Storage SR]

Service Manual
3.17.12 DICOM information change

Select service on the screen and then press [Edit]. Information of selected service
appears. To save the information after changing, press [Save]. To cancel, press[Cancel].
3.17.13 DICOM service delete

Select service on the screen and then press [Delete].
3.17.14 DICOM server test

Select service on the screen and then press [Test]. Test the connection status with
selected service and display the result in Ping and Verify items. If appearing as Normal,
it is the normally connected status.
3.17.15 DICOM management

If pressing [Queue] on the screen, it is converted to DICOM Job Status screen. You
review the current situation of Job through Job ID, Patient ID etc.
Configuration of DICOM Job Status screen is as follows.
[Figure 7.22 DICOM Job Status]

① Job ID: displays Job number.

② Patient ID: displays patient ID.
③ Alias: displays Alias value set in DICOM Configuration screen.
④ Type: displays the types of job. The types of jobs are Storage, Print, Storage SR,
MPPS Start, MPPS End, Storage CMT etc.
⑤ Instances: The number of objects is displayed. The target of Instance isdifferent
depending on Job Type. In case of Storage and Print, Instancemeans the number of
images and Storage SR means Measure Data. Incase of MPPS Start, Instances are
always displayed as 0.
⑥ Data/Time: displays time and date when Job is created.
⑦ Status: displays the current status of Job
Status Description
Fail Failure to perform
Transfer In progress
Imperfect Suspended while performing. Soon it is converted to Ready

status.
Wait Waiting for performance
Wait Resp Waiting for response
Hold Holding. This is the case that when Job failed, Retry Count
is left.
Ready Waiting for performance. This is the case that network is not
linked.
Not Ready Waiting for performance is not completed. This is the status
before MPPS(Modality Performed Procedure Step) Start is
completed. Or this is the case that Print Job or Storage
selected by Batch is not terminated.
Network Status
Network connection status is displayed. If connected, it is displayed as ‘Connected’, if
not connected, it is displayed as ‘Disconnected’
Number of Jobs
The number of jobs displayed on DICOM Job Status screen is displayed.
Log
DICOM Log window appears.
Retry

Service Manual
You can retry selected Job. Button is activated only when Status of selected Job is Fail
or Waiti Resp.
Retry All
You can retry all jobs whose status is fail.
Delete
You can delete selected job. Button is activated only when Status of selected Job is Fail
or Imperfect, Waiti Resp, Not Ready
Clear
You can clear all Jobs.
3.17.16 DICOM Log

If pressing [Log] on DICOM Job Status screen, DICOM Log window appears. You can
manage the history of all DICOM services performed in this product.
Log Settings
You can set the management method of Log file.
- Delete Archived Log Afterwards: Sets the storage period of Log file. It is input as
numbers and the unit is day. If the period as long as set elapses after Log file is made,
it deletes file from the system.
- Log File Maximum Size: Sets the maximum size of Log file to be archived. It is input as
numbers and the unit is Kbytes. Log file of the size set or larger is deleted immediately
without being saved in the system.
DICOM Log
Information of Log file is displayed..
- Select All: selects all Log files.
- Delete Selected Files: Deletes selected Log files.
- Copy Selected Files: Copies selected Log files in external storage media.
- View Selected File: displays detailed information on selected Log file on the screen
- Refresh: updates information of Log file.

[Figure 7.23 DICOM Log]

Service Manual
3.18 Auto Calc

Select [AutoCalc] tab on Setup screen. Or press [AutoCalc] of touch screen.
AutoCalc is the function supported in spectral Doppler mode and calculates particular
items automatically by using measured values.
．．．．
NO T E
• Set items appear on the screen only when pressing [Auto Calc] of touch screen in
spectral Doppler mode.
[Figure 7.24 Setup-AutoCalc]
3.18.1 AutoCalc. Setting

Set items to perform automatic calculation by selecting the checkbox or lift setting. You
can select up to 6 items. When Peak Systolic Velocity and End Diastolic Velocity value
is 0, the result values of all items do not appear on the screen.
Also, the result value of Timed Averaged Mean Velocity is displayed only when Mean
Trace is On.

3.18.2 System information (About)
Select [About] tab in Setup screen. Or press [About] of touch screen.
S/W version information of the product is shown.
If pressing [Detail], you can check detailed Version related to the product.
[Figure 7.25 Setup -Information]

* S/W version of the above figure may differ from the actual system version.

Service Manual
3.19 Measure Setup

You can set various items related to measurement. You can change depending
on your needs or tastes.
1. Press Utility > Measure Setup in touch screen.
2. If Measure Setup screen appears in monitor and touch screen, select tab where an
item to be set belongs.
3. Set to fit each item.
4. Save setting and then close. If pressing [Close] of monitor screen or [Close] oftouch
screen, [Exit] of control panel, it is switched to scan mode. If pressing [Return] of
touch screen, it goes back to Utility screen, the previous step.
※ Tips! – How to choose tab
You can select the tab you want with the following two methods. Select the
method you like.
- Select the tab of monitor screen by using trackball and [Set] button.
- Press button on touch screen.
[Figure 7.26 Measure Setup-touch screen]

3.19.1 Measure Menu
Press Utility > Measure Menu on touch screen. Monitor and touch screen are switched
to Measure Menu screen. Set buttons to appear on touch screen when measuring. You
can configure and select menus on measurement items and results etc. to suit your
preference.
[Figure 7.27 Measure Menu]
3.19.1.1 Select Calc Page

You can select measure page to be set (Package). Or you can select by turning dial-
button [1] Page of touch screen.
Measure page is composed of OB, Gynecology, Cardiac, Vascular, Fetal Heart, Urology,
Abdomen, Small Parts, TCD, Pediatric Hips, MSK.
3.19.2 Available Menu List

It is the menu of Touch Page and possible measurement items appear.
If pressing ‘+’,sub measurement items appear. Select measurement items on [Available
Menu List] and location and then press ⇨ of the screen. Selected items are created on
the right menu.
3.19.2.1 Touch Menu Design

 Measurement package setting
- Prev Page: Goes to previous page.
- Next page: Goes to next page.

Service Manual
 Menu location change

After selecting measurement group or item, you can change the location by using ⇦,
⇨, ⇧, ⇩.
 New Tab
You can create new tab.
 Delete Menu
You can delete selected measurement item.
 Rename Tab
You can change the name of created tab.
 Clear All
You can delete all contents of selected tab.
 Save this Page
You can save changes of the current page.
 Default Items
If pressing [Default Items] of the screen, it is initialized to default setting.
 Return
You can return to previous step of the current menu.
 Close
You can close editing. If there are changes, the message asking whether to save
appears.
．．．．
NO T E
• You cannot place sub measurement items in Group.
• For more information on measurement items, see ‘Chapter 5 Measurement’.
[Figure 7.28 Measure Menu –touch screen]

3.19.3 Measurement general setting (General)
Select [General] tab in Measure Setup screen. Or press [General] of touch screen. Set
default items used when measuring.
General Setup
Select [General] tab among sub tabs belonging to [General] tab.
Conduct the most basic setup related to measurement.
[Figure 7.29 Measure Setup - General - General]
3.19.3.1 Cursor & Method

Line Marker Type
You can set the shape of Caliper Cursor appearing on the screen.
Select one between cross(+) shaped ‘Cross Hair’ and arrow shaped ‘Arrow Head’
Circ and area method
You can set the method to be used to measure Circumference and Area.
Select one between Ellipse and Trace. The selected measurement method is set to
appear first when pressing [Caliper] button. Therefore, if setting the commonly used
measurement method, you can start measuring conveniently.
For more information on Ellipse and Trace, see Circumference and Area
measurement of Chapter 5.
Apply Auto Marker Cursor Size
When measuring if the distance between start point and moving point is less than50
pixel, you can set whether to use the function automatically reducing Cursor Size of

Service Manual
Marker
3.19.3.2 Line Type

When measuring the distance, you can select pattern of line among the following three.
Dotted Line
Line is displayed as dotted line.
Hidden Dotted Line
Only start point and end point are displayed.
Hidden Dotted Line after Set
Line is displayed as dotted line only while drawing lines and if lines are completed by
pressing [Set] button, dotted lines are hidden.
※ Tips! – Line Type select
If selecting Hidden Dotted Line or Hidden Dotted Line after Set, you can
prevent images from being covered by measurement lines.
3.19.3.3 Start Point of Measurement

You can set the position where measurement cursor appears. When measuring, set the
position of start point.
- End Point of the Last: Cursor appears at endpoint position of last performed
measurement.
- Start Point of the Last: Cursor appears at start point position of last performed
measurement.
- Center of the Region: Cursor appears in the middle of image area.
3.19.3.4 Display
You can set items to be displayed on the screen while measuring. Select check box for
items to be used.
Guideline
Display the Doppler Guideline: Sets whether to display Cross line when measuring
various items in spectrum of Freeze state.
This function is useful in estimating the approximate value.
Display the M-Mode Guideline: When measuring various items in Freeze state of M
mode, you can set whether to display Cross line. This function is useful in estimating the
approximate value.

Clear Function on Unfreez
Clear Measure 2D Mode Result On Unfreeze: When converted to scan mode after
performing measurement in 2D mode, you can set whether to
clear screen measurement results.
Clear Measure M/D Mode Result On Unfreeze: When converted to scan mode after
performing measurement in M mode and Doppler mode, you can set whether to
clear screen measurement results.
Measurement Unit
You can set measurement unit. It is convenient to use mm unit in Dist for small object to
be measured and if blood flow speed is fast, it is useful to use m/s unit in Vel.
- Dist: Select unit of distance, area, volume from cm scale and mm scale.
- Vel: Select unit of speed from cm/s and m/s.
．．．．
NO T E
• If changing measurement unit, all of the result values measured so far will be deleted.
Measurement Results
- Transparent BK color: sets transparency of screen background.
- Number of Measure Results Displayed: Sets the number of lines of measure results to
be displayed on the screen. It is applied to all diagnostic subjects and basic measure
results except for obstetrics, cardiac, vascular, urology, fetal echocardiography
measurements
Report
Select [Report] tab among sub tabs belonging to [General] tab. Set items related to
measure report.

Service Manual
 Use SonoReport
Use the form provided by SonoReport not the report form provided by Samsung
Medison Co., Ltd.
．．．．
NO T E
• But, it is available only where there is the program provided by SonoReport. For more
information, contact customer support center of Samsung Medison Co., Ltd. in your
area.
[Figure 7.30 Measure Setup - General -Report]
▐ Report Header
You can set information to be displayed in the report header.
You can set several items and set items are commonly displayed in all measure reports.
3 Hospital Info
This is information on hospitals where the product is installed.
You can select Hospital name, Diag. Physician, Ref. Physician, Sonographer.
4 Patient Info
This is information on patients. You can select ID, name, Gender, Heart Rate, Birthday,
Age, BSA.
5 Others
This is information related to other comments. You can select Description and Accession
#.

▐ Measurement Result
 Measurement Result Type:
Sets calculation method of measurement value written in the report.
- Avg; represents average value on 3 values recently measured.
- Last; represents measured value at the end
- Max; represents the largest value of measured values.
- Min; represents the smallest value of measured values.
▐ Print Action
6 Print All Report Pages: Prints all reports
7 Print Current Pages: Prints the current page
▐ Save Action
8 Save All Report Pages: Saves all reports
9 Save Current Pages: Saves the current page.
▐ OB / FH Header layout
You can set items to be displayed in header of obstetrics
or fetal echocardiography measurement report. You can select various items.
EFW Pctl. (EFW)
GA (EFW) SD (EFW)
Gravida Aborta
Para Ectopic
Data Transfer
Select [Data Transfer] tab among sub tabs belonging to [General] tab. Set how to
transfer data etc.

Service Manual
[Figure 7.31 Measure Setup - General –Data Transfer]
▐ Serial Transfer
Set the format of the data to be transferred. Select between Text Format and XML
Format. This product transfers data by using RS-232C serial cable for USB. If you try to
transfer data by using reporting tool such as Astraia, Sonoultra, Viewpoint, select XML
Format.
．．．．
NO T E
• Before setting, check if [COM] is selected as ‘Open Line Transfer’ in Peripherals tab of
Setup screen.
▐ User Table Backup & Restore

Backup Table that you made or restore backed up Table in the system.
Set properly in the screen appearing after pressing [Back Up] or [Restore].
▐ DICOM SR Format
■ General Report: format method of default setting
■ View Point: View Point data format method
Caliper
Select [Caliper] tab among sub tabs belonging to [General] tab.

Set whether to also display additional information other than basic measured values
wen performing basic measurement by pressing [Caliper] button of control panel.
If using this function, it is also displayed when storing or printing measure results.
If setting ‘Application’ as Cardiac, items such as ‘D Velocity’, ‘D A/B’, ‘D Trace’, ‘M
Distance’ are changed.
．．．．
NO T E
• You can use ‘Cardiac’ setting only when setting value of probe is Cardiac or Pediatric
Cardiology
[Figure 7.32 Measure Setup - General –Caliper]

Obstetrics (OB) measurement setup
Select [OB] tab in Measure Setup screen. Or press [OB] of touch screen.
Set items related to obstetrics measurement.
General setup (General)
Select [General] among sub tabs of [OB]. Set basics related to obstetrics measurement.

Service Manual
[Figure 7.33 Measure Setup – OB - General]
▐ Percentile Information
10 Show Percentile Information
Set whether to use of Percentile Information by using the checkbox.
11 Percentile Criteria
Select the value to be used in Percentile calculation.
- GA by LMP: Calculates GA(Gestational Age) based on LMP of mother
- Estab. Due Date: Estab of mother filled out in Patient Information
- Calculate GA based on Due Date.
- AUA (Average US GA): Calculates GA by using average value of a few items
measured by using ultrasound waves.
12 Rank Information Method
You can set the method displaying Growth Range information. You can
observe developmental degree of fetus and whether normal or not by using Growth
Range.
- Standard Deviation: Developmental degree of fetus and whether normal or not is
observed based on SD=0, standard developmental state.
- Pctl.: Developmental degree of fetus is displayed in Percentile. Developmental degree
of fetus and whether normal or not is observed based on 50%,
standard developmental status.
- Bar (Graph): Displays Percentile in Bar graph. This method can be used only in
obstetrics report. Green represents the range of normal development and red

expressed at front and rear based on green represents the range of abnormal
development
▐ Fetal Weight Unit

You can set the unit of fetal weight to be used in obstetrics measurement.
You can set by dividing it into basic unit and auxiliary unit and display measure results in
several units.Basic unit can be set as one between ‘Gram [g]’ or ‘lb +oz’ on the
left. Auxiliary unit is set in unit representation of the right and set by excluding unit
representation selected as basic unit. ‘lb +oz’ is unit representation displaying
both Pound and Ounces and ‘None’ means that auxiliary unit is not used.
▐ Clear Function on UnFreeze

This function is applied only in obsterics.
13 Clear Measure 2D Mode Result On UnFreeze
When unfreezing after measuring by using the checkbox, set whether to delete 2D
mode Result.
14 Clear Measure M/D Mode Result On UnFreeze
When unfreezing after measuring by using the checkbox, set whether to delete Mmode
or D mode Result.
▐ Number of Measure Results Displayed

15 Number of Results Displayed
You can set the number of lines of obstetrics measure result to be shown in thescreen.
▐ OB Doppler Results
You can set Display by each item for Doppler Result to be shown in the screen of OB
package
PSV : Disabled PGmean: Enabled
EDV: Disabled S/D : Enabled
TAPV: Enabled D/S : Enabled
TAMV : Enabled PI: Enabled
PGmax: Enabled RI: Enabled
▐ OB Measurement Result
16 Measurement Result Type

Service Manual
Set measurement result type. Select one among average

(Avg), last measured value (Last), maximum (Max), minimum (Min).
Tables setup
Select [Tables] from sub tabs of [OB]. Set reference such as equation and Reference
table etc. to be used in each measure item.
[Figure 7.34 Measure Setup – OB -Tables]
17 Items
This is setup to measure the size of fetus (Growth) or Gestational Age (GA). Select
itemsaccording to the following procedure.
1. Select measure items from the list on the left.
2. Select table type to be used between GA table and Growth table.
3. Select reference from the list appearing on the right.
18 Fetal Weight
This is setup to measure Estimated Fetal Weight (EFW). Select items according to the
following procedure.
- Select the method measuring EFW between EFW equation and EFW growth.
- Select reference to be used from the list appearing below.
19 Add reference
．．．．
NO T E
• When adding Table reference, note the following..

• If not satisfying the following conditions, the warning message appears and reference
is not saved.
- Enter more than minimum 3 data.
- If there is not Min, Max value, select ‘Table Type’ as Value Only
1. Press . User reference window appears.

2. Enter Name and Description of new reference.
3. Select the type of reference from Table and Equation.
．．．．
NO T E
• EFW Equation supports only Equation reference type and EFW Growth supports only
Table.
4. Press [Ok] to move on to next step. The screen is switched to Editor screen. Press
[Cancel] to cancel.
5. Enter reference.
6. Press [Save] to save contents. Press [Cancel] to cancel.
7. Press [Ok] to complete input. Press [Cancel] to cancel.
[Figure 7.35 User Reference]
※ Add reference table

If pressing the question mark button, the source of reference is shown.
If pressing the question mark button again, source marking disappears.

Service Manual
[Figure 7.36 User Table]
Unit Information
The unit of selected reference such as Input, Output, SD etc. is displayed.

Table type
You can set the type of table for selected reference. In case of Growth Table,
SD(Standard Deviation) is displayed.
- Range Type: Sets Min., Max value of selected reference and represents it as table.
SD value appears by being changed depending on the scope set by a user.
- Value Type: Represents only measured value entered by a user regardless of the
range of Min., Max., SD etc.
Others
- Show In Days: If selecting the checkbox, the unit of Table is changed from
wd(Week-day) to d(day) and displayed as such.
- Cursor Movement for [Enter] key: Sets the moving direction of cursor when
pressing [Enter] key of keyboard while editing Table. Select one from Right, Down,
Edit.
※ Add Reference Equation
Enter the following information

Equation
Input reference equation. Use measurement calculator shown in the right

bottom.
Input Value Ranges
Input low, high range of selected measurement references.

Tolerance Information
For Tolerance Information, select one between w and d.
[Figure 7.37 User Equation]
20 View and modify references

1. Select Preset in Selection
2. If pressing , Editor screen for reference appears.
3. View or modify references.
21 EFW Sequential Measurement
．．．．
NO T E
• It is the setting needed when selecting User Key1 or 2 as ‘EFW Measure’ in [Utility] >
[Setup] > [User Defined key] > [User Key Setup]
• Set contents are applied when measuring EFW by using [User 1] (or [User 2]) button.
• You can set EFW measure in Touch Menu Designer. For more information, see ‘Touch
Menu Designer’ of this chapter.
When measuring EFW by using [User 1] (or [User 2]) button, set the order of
measurement items. Select measurement items by using trackball and [Set] button and
then, change the order by using arrow.
Calc & Graph

Select [Calc & Graph] among sub tabs of [OB]. Set for calculations and graph.

Service Manual
[Figure 7.38 Calc & Graph]
▐ Auto calculations
Items to be calculated are set automatically. For example, if selecting MAD checkbox in
the following figure, measurement of APD and TAD is completed and then,by using this,
MAD is calculated automatically and displayed on the screen.
Result value of auto calculations may affect GA, EDD information.
▐ Ratio calculations
Measurement items to calculate ratio are set. For example, if selecting FL/BPD check
box in the following figure, measurement of FL and BPD is completed and then, the ratio
of these is calculated automatically and displayed on the screen. This ratio is also
recorded in the report.
▐ Fetal Doppler trend graph

You can set whether to include PI, RI graph of MCA(Mid Cerebral Artery),
UA(Umbilical Artery) in the obstetrics report. If pressing , Editor screen on the graph
appears.
▐ Trend graph
You can set whether to include the graph of a particular item or percentage
in the obstetrics report. If pressing , Editor screen on the graph appears.
Cardiac measure setup

Select [Cardiac] tab in Measure Setup screen.

Or press [Cardiac] on touch screen. Set items related to cardiac measure.
[Figure 7.39 Measure Setup - Cardiac]
▐ Cursor & Method

22 Circ. and Area method
You can set the measurement method to be used when measuring circumference and
area for 2D image of heart. Select one between Ellipse method and Trace method..
23 LV Volume Method
You can set the measurement method to be used when calculating the volume of the
left ventricle among Teichholz, Cubed, Gibson.
For more information on calculation formula, see the reference manual.
▐ Cardiac Measurement Result


Service Manual

Set the number of lines of measure results to be displayed on the screen.
▐ Type of Derived Calc Results Displayed

Set display type of measure results. Select ‘Brief’ to display briefly and ‘Detailed’ to
display details.
Vascular measure setup (Vascular)

Select [Vascular] tab in Measure Setup screen.
Or press [Vascular] of touch screen. Set items related to vascular measure.
[Figure 7.40 Measure Setup - Vascular]
▐ A/B Ratio
Set Velocity to calculate ratio in A, B one by one.
▐ ICA/CCA Ratio
Set measure items to be used in ICA/CCA ratio one by one.
▐ Doppler Results
Set Doppler measure items to be displayed with measure results.

▐ Vascular Measurement Result
Set measurement type. Select one among average (Avg), last measured value (Last),
maximum (Max), minimum (Min).


Service Manual
Urology measure setup

Select [Urology] tab in Measure Setup screen. Or press [Urology] of touch screen. Set
items related to Urology measurement.
[Figure 7.41 Measure Setup - Urology]
▐ Volume Method
Set the formula to be used when calculating volume.
- 3 Distance: Volume value is calculated by using three diameters in Transversal plane
and Longitude plane (4 / 3 x π x A/2 x B/2 x C/2).
- 3 Distance x Factor: Three diameters are calculated in Longitude plane and
Transversal plane and volume value is calculated by using factor (F) value entered by
a user. ( A x B x C x Factor)

- Ellipsoid: Volume value is calculated by using the length of Beside axis and the length
2
of Main axis in 2D plane (4 / 3 x π x Main / 2 x (Beside / 2) ).
- Sum of 20 Disks: Volume value is calculated by adding areas in 20 parallel planes (d /
20 x (A1 + A2 + ... A20), d : Total of distance between disks)
．．．．
NO T E
st nd rd
• 3 Distances * Factor: A = 1 Dia. ; B = 2 Dia. ; C = 3 Dia.
• Factor value is basically set as ‘0.523’. If trying to set by changing the value, the
value of ‘0 < factor <= 1’ is recommended.
▐ Predicted PSA correction factor

You can set Predicted PAS correction factor to measure the volume of T-Zone and WG
volume. Default value is set as 0.12.
▐ Urology Measurement Result


You can set the number of lines of urology measure results to be shown on the screen.
Fetal echocardiography measurement setup (Fetal Heart)

Select [Fetal Heart] tab in Measure Setup screen. Or press [Fetal Heart] of touchscreen.
Set items related to fetal heart measurement.
▐ Cursor & Method

30 Circ. and Area Method
You can set the measurement method to be used when measuring circumference and
area for 2D image of fetal heart. Select one between Ellipse method and Trace method.
31 LV Volume Method
You can set the measurement method to be used when calculating the volume of the
left ventricle among Teichholz, Cubed, Gibson. For more information on calculation
formula, see the reference manual.

Service Manual
▐ FH Measurement Result
Set measurement type. Select one among average (Avg), last measured value (Last),
maximum (Max), minimum (Min).

[Figure 7.42 Measure Setup - Fetal Heart]

3.20 Utility
This is the menu to set the system or use ECG, Biopsy, Histogram etc. How to use the
Utility menu is as follows.
1. Press [Utility] on touch screen. Utility screen appears on touch screen.
2. Select an item you want to use by pressing button.
3. Press [Return] to return to Utility screen after use. Press [Exit] button of control panel
or [Exit] of touch screen to exit Utility screen and switch to scan mode.
[Figure 7.43 Utility-touch screen]
▐ Key Volume
Set button sound of touch screen. Select one from 0 to 100 by using dial-button of touch
screen. If setting to 0, it is the state not using button sound.

Service Manual
Post Curve
Press [Post Curve] on touch screen. Touch screen is converted to Post Curve.
Set various post maps and Gamma values.
[Figure 7.44 Post Curve-touch screen]
▐ 2 D Post
Press [2D Post].
34 Chroma Map
Turn on/off by pressing [Chroma Map] of touch screen. In On state, you can randomly
change colors of on-screen images. Select one between Type 1~13 or User 1~3 by
using dial-button [1]. If setting Curve as User type, [Chroma Map Edit] of touch screen is
activated.
35 Chroma Map Edit
Set and use Chroma color according to your preference. You can set it in the menu of
each diagnostic mode. It is activated only in [User] type. Adjust colors by using [Red],
[Green], [Blue]. You can set from 0 to 255. If changing setting, [Chroma Map Save] is
activated. Press [Chroma Map Save] to save setting.
36 Chroma Map Save
Save setting changed in [Chroma map Edit].
37 Return
After completing setting of current Post Map, return to the previous step of the current
menu.
38 Gamma
Set brightness and light and shade contrast by using dial-button of touch screen (Off,
Weak, Medium, Hard).

- Off: Not using Gamma function
- Weak: Function viewing by adjusting contrast brightly
- Medium: Function viewing by adjusting contrast to the medium
- Hard: Function viewing by adjusting contrast darkly
[Figure 7.45 2D Post-touch screen]

Service Manual
▐ Color Map
Press [Color Map].
39 Tag
Turn on/ off by pressing [Tag] of touch screen. You can randomly change the color of a
certain part (Tag) of on-screen image.
40 Tag Width
Set the range of Tag from 8 to 256 by using dial-button of touch screen. If changing Tag
Width, Tag Pos can be changed.
41 Tag Pos
Set the position of Tag from 0 to 248 by using dial-button of touch screen. If changing
Tag Pos, Tag Width can be changed.
42 Color Map
Select type of Color Map by using dial-button of touch screen. 14 types preset in the
system are supported.
[Figure 7.46 Color Map-touch screen]
▐ M Post
Press [M Post]. Various setting methods are the same as 2D Post.
▐ D Post
Press [D Post]. Edit method is the same as 2D Post

▐ Monitor Calibration
Press [Monitor Calibration].
43 Brightness
Set brightness of screen. Select one from 0 to 100 by using dial-button.
44 Contrast
Set light and shade Contrast of screen.
Select one from 0 to 00 by using dial-button
45 Curve
Set post curve. Select one between Type 1~5 or User 1~3 by using dial-button. You can
set User Type as you want by using [Edit].
 Edit
If setting Curve as User, [Edit] of touch screen is activated. If pressing [Edit] of touch
screen, screen and menu to set curve appear.
- Insert: Adds a point to curve. A new point is added between currently selected point
and next point.
- Delete: deletes currently selected point.
- Save: saves current curve.
- Picker Pos: selects one point in Curve. You can select position of point by using dial-
button.
- Color: Sets a color of point on Curve among [Red], [Green], [Blue] according to your
preference.
46 Default
Changed into initial setting when released from the factory.
[Figure 7.47 Monitor Calibration –touch screen]

Service Manual
ECG
Press [ECG] of touch screen. The image of heartbeat is shown.
[Figure 7.48 ECG-touch screen]
．．．．
NO T E
Menu is shown when diagnostic subject is set as Cardiac or Vascular.
You can use ECG CINE function for each image in multiple image mode such as Dual,
Quad etc.
▐ ECG start and shutdown

Press [ECG] on touch screen.
▐ ECG setup
47 ECG Invert
You can invert ECG. Turn on or off by pressing touch screen.
48 Auto Gain
If pressing [Auto Gain] of touch screen, Gain value of ECG is automatically set.
49 2D / Loop
You can set the area to use ECG. Select [2D] or [Loop] by pressing touch screen. [2D]
uses ECG in 2D area and [Loop] in the Loop area of spectral Doppler mode.
50 Sweep Speed
You can set the pace of ECG

Select one from 60Hz, 120Hz, 180z, 240Hz, 300Hz, 360Hz by using Dial-button of
touch screen.
51 Trigger
You can set Trigger Interval. Select between 1~5 or turn off by using dial-button of touch
screen.
52 Trigger Time
You can set time to perform Trigger. Select one from 0 to1000 msec by using dial-button
of touch screen.
53 Gain
You can set Gain value of ECG. Select one from 10 to 100 by using dial-button of touch
screen.
54 Size
You can set the size of ECG. Select one from 50-200 by using dial-button of touch
screen.
55 Position
You can set the position of ECG. Select one from 0 to 90 by using dial-button of touch
screen. As the number is higher, ECG is located at the top of the screen.
．．．．．．．
CAUTION
• If ECG is less than 30Hz, Heart Rate(HR) may not work.
• In CW mode where ECG is working, the error rate of Heart Rate(HR) value is within
2%.
Histogram
Histogram is a kind of graphs and shows the distribution of echo.
1. Press [Histogram] on touch screen. Touch screen is converted to Histogram.
2. Designate the area to show histogram. Set area 1, 2, 3 in monitor screen by using
3. Histogram 1, 2, 3 is shown in screen.

Service Manual
[Figure 7.49 Histogram]
▐ Histogram setup
You can set the position or type of Histogram.
56 Move Hist. 1, 2, 3
Select Histogram to move by pressing the button of touch screen and then, change
moving position by using trackball and [Set] button.
57 Rectangle, Ellipse
[Rectangle] or [Ellipse] of touch screen sets the area shape of Histogram
Select one from Rectangle and Ellipse.
[Figure 7.50 Histogram-touch screen]

Biopsy
Select [Biopsy] of touch screen.
．．．．
NO T E
Before using Biopsy, be sure to adjust Biopsy guildelines.
[Figure 7.51 Biopsy]
▐ Biopsy guideline setup
．．．．
NO T E
• If you are using Trapezoidal function of linear probe, you cannot set Biopsy guidelines.
• If rebooting the system, Biopsy guidelines can be restored to default.
1. Press [Edit]. The warning message appears.

2. If pressing [Ok], the screen to set guidelines appears.
3. You can set Biopsy guidelines by using trackball and [Set] button.
4. Press [Save] of touch screen to save setup. The OK message appears.
- Press [Edit] to reset.
5. If pressing [Ok], set Biopsy guidelines are applied. Press [Cancel] to cancel saving.
※ Multi guideline support

If using Biopsy of particular probe (C), [User] allowing you to preset and use

Service Manual
Biopsy guidelines appears on touch screen.
※ Setting user guideline

Select Biopsy guidelines to be set by using [User] of touch screen.
1. Press [Edit]. The warning message appears.
2. Press [Save] of touch screen to save setup. The OK message appears.
- Press [Edit] to reset.
3. If pressing [Ok], set Biopsy guidelines are applied. Press [Cancel] to cancel
saving.
▐ Biopsy start and shutdown

1. Press [Biopsy On/Off] of touch screen. A message appears.
2. If pressing [Ok], Biopsy guidelines appear on the screen.
- If guidelines displayed on the screen are incorrect, press [Edit] to reset.
- If using probe supporting multi guidelines, you can select and use guidelines
preset by using [User].
3. Insert Needle into the body according to guidelines. After that, conduct proper Biopsy.
4. After all the procedures, press [Biopsy On/Off] again. Biopsy is terminated.
[Figure 7.52 Biopsy-touch screen]

DVR
Press [DVR] of touch screen. Touch screen is converted to DVR screen.
．．．．．．．
CAUTION
Before you start recording, be sure to check the capacity of media.
▐ Record
You can record images in DVD format.
58 Record
If pressing button (①), recording preparation is started and as soon as preparation is
finished, you can start recording. Time to start recording may differ depending on kinds
of DVD media.
59 Record Stop
If pressing button (②), recording is stopped.
60 Close Session
If pressing button (③), current recording mode is closed. To play recorded images,
you should close current recording mode by pressing [Close Session] with recording
stopped.
61 Record Mode
Set t recording method between Append and Overwrite by using dial-button or pressing
touch screen.
- Append: Recording following the current recorded contents
- Overwrite: Newly recording after clearing the current recorded contents
▐ Play
You can play recorded images.
62 Play
Press button (④) to start play.
63 Pause
Press button (⑤) to pause.
64 Stop
Press button (⑥) to stop play.
65 Rewind
Press button (⑦) to perform rewind.

Service Manual
66 Fast Forward
Press button (⑧) to perform fast forward.
67 Speed
Set speed of Rewind or Fast Forward. Select one between x4, x8 by pressing touch
screen or using dial-button.
▐ Eject Tray
Press the button of touch screen to eject media tray.
▐ Close Tray
Press the button of touch screen to close media tray.
▐ Volume
You can adjust volume of vide being played. Select one from 0 to 100 by pressing touch
screen or using dial-button.
[Figure 7.53 DVR-touch screen]
．．．．
NO T E
• For more information on recommended media, see ‘peripheral devices’ of ‘Chapter 2
about product’.
• We guarantee the following media.
:Mitsubishi+RW, Imation+RW, HP+RW, Melody+RW
• Media recorded through ADVR are not backed up or transferred. Also, media backed
up or transferred media through ADVR are not recorded.

Ez Exam Setup
Press [Ez Exam Setup] of touch screen. Ez Exam Setup screen appears on monitor
screen and touch screen. Ez Exam Setup is the function setting Exam items and the
order that you want. This function helps to improve efficiency of diagnosis.
[Figure 7.54 Ez Exam Setup]
▐ Application List
The list of available diagnostic subjects appears. If there is EZ Exam which is already
set, when you select a diagnostic subject, it is displayed in EZ Exam List.
68 Default
You can initialize Exam of selected diagnostic subjects. All Exams in User List of EZ
Exam List are deleted.
▐ EZ Exam List
EZ Exam list appears.
69 Default List
EZ Exams basically supported in the product are displayed. They are only supported in
Gynecology, Vascular, SmallParts.
You cannot delete EZ Exams in Default List or change their names.
Also, you cannot add new EZ Exams in Default List.
70 User List.
EZ Exams set by a user are displayed.
You can delete, copy or change the names of EZ Exams in User List and add new EZ
Exams.

Service Manual
71 Add EZ Exam
Press [New] of touch screen or monitor screen. If New Tap window appears, enter
name and then press [OK]. Press [Cancel] to cancel.
72 Copy EZ Exam
Select EZ Exam to be copied and then, press [Copy] of touch screen or monitor screen.
If Copy Tap window appears, enter name and then, press [OK]. Press [Cancel] to cancel.
73 Change EZ Exam name
Select EZ Exam you want to rename and then, press [Rename] of touch screen or
monitor screen. If Copy Tap window appears, enter name and then, press [OK]. Press
[Cancel] to cancel.
74 Delete EZ Exam
Select EZ Exam to be deleted and then, press [Delete] of touch screen or monitor
screen. If Warning window appears, press [OK]. Press [Cancel] to cancel.
75 Change EZ Exam order
Select EZ Exam that you want to change the order and then press or of
monitor screen.
▐ EZ Exam Preview
Previews detailed items and group of EZ Exam that you selected. The groups belonging
to EZ Exam are displayed as . Press to see sub items of group.
76 Add Group
You can add group. Press button of monitor screen or [Add Group] of touch
screen. If New Group window appears, enter name and then press [OK]. Press [Cancel]
to cancel.
．．．．
NO T E
• Only EZ Exam in User List can add group.
77 Edit Setting
You can change the properties of items selected in Misc.of Action List.
- Annotation: Sets text to be entered in the screen. If pressing [Edit Setting] of touch
screen after selecting Annotation, Text window appears. Enter text and then press
[OK]. Press [Cancel] to cancel.
- Body Marker: Sets Body Marker to be entered in screen. If pressing [Edit Setting] of
touch screen after selecting BodyMarker, BodyMarker screen appears on touch
screen. Set Body Marker and then press [Exit].
- Caliper: Sets basic measurement items to be used. If pressing [Edit Setting] of touch

screen after selecting Caliper, Caliper Selection screen appears on touch screen.
Select item to be used and then press [OK]. Press [Cancel] to cancel.
- Mode Control: Sets diagnostic mode to be used. If pressing [Edit Setting] of touch
screen after selecting Mode Control, Mode Selection screen appears on touch screen.
Select item to be used and then press [OK]. Press [Cancel] to cancel.
78 Edit Name
- You can change the name of group. Select group and then press [Edit Name] of touch
screen. If Edit MacroName window appears, enter name and press [OK]. Press
[Cancel] to cancel.
79 Change the order
Select an item or group that you want to change the order, press or of
monitor screen.
▐ Action List
Shows detailed items that can be added to selected EZ Exam. Select the tab you want
and then select detailed items. Press to see sub items.
80 Add item
Select items in Action List and then press . Selected items are added to EZ Exam
and and shown in EZ Exam Preview. Up to 40 items can be added to one group.
81 Delete item
Select item in EZ Exam Preview and then press . The seleted item is deleted from
EZ Exam.
[Figure 7.55 Ez Exam Setup-touch screen]

Service Manual
Help
Press [Help] of touch screen. Help saved in the system appears on the monitor screen.
Storage Manager
Press [Storage Manager] of touch screen. All disk drives mounted in the system appear.
Drive type, available capacity and the full capacity of drive are displayed.Storage
Manager is the program managing various storage devices connected to the
system. The drive with checkbox in front of drive symbol can perform management such
as refresh, format, update etc.
．．．．
NO T E
• A drive mounted in the computer of the system cannot perform management such as
remove, format, refresh etc.
Press [Exit] of touch screen to exit Storage Manager. Or press [Exit] button of control
panel.
82 Refresh
You can refresh a drive connected to the system and show it on the screen.
．．．．
NO T E
• While using Storage Manager, information is refreshed only by pressing [Refresh].
83 Eject / Remove
You can remove connection of selected drive.
．．．．
NO T E
Before ejecting USB Flash memory drive device, be sure to remove connection by
using [Eject / Remove].
84 Format
- You can initialize selected drive. You can perform initialization by selecting various settings
in Format window. Press [Start] to start initialization. Press [Cancel] to cancel.
．．．．
NO T E
• In case of DVD+RW, DVD-RW media, available capacity of media may be displayed
TM
as O bytes after format. This is an error occurring in Windows and there is no
problem to use actual media.

[Figure 7.56 Storage Manager]

Service Manual
Power Management
Press [Power Management] of touch screen. Touch screen is converted into Power
Management.
▐ TI Display
Set TI from TIs(Soft tissue thermal Index), TIb(Bone thermal index), TIc(Cranial bone
thermal index) appearing on the screen.
85 Save
Press the button of touch screen to save changed contents.
86 Power
You can select intensity of ultrasound output.
Select one from 10 to 100 by pressing the button of touch screen or using dial-button.
[Figure 7.57 Power Management]

Chapter 4
Product inspection
Service Manual
Chapter 4 Product inspection
4.1 Overview
Chapter 4 describes the contents checking if important functions and power etc. are
operating normally after installing A30.
Contents
4.1 Overview .................................................................................................................. 4-1

4.2 Turning on the product ............................................................................................ 4-2
4.3 Monitor ...................................................................................................................... 4-3
4.3.1 Screen configuration ................................................................................ 4-3
4.4 Control panel............................................................................................................ 4-5
4.4.1 Detailed functions of control panel .......................................................... 4-6
4.4.2 Keyboard ................................................................................................... 4-8
4.4.3 Touch screen ............................................................................................. 4-9
4.4.4 Adjustment of control panel ................................................................... 4-10
4.5 Performance checking ........................................................................................ 4-11
4.5.1 Basic checking ........................................................................................ 4-11
4.5.2 Detailed checking ................................................................................... 4-12
Chapter 4 Product inspection 4-1

4.2 Turning on the product
1) Check once again if power capacity of A30 is right and connect power plug to
power outlet.
2) Check if A30 and power cable were connected properly and turn on the switch
of power circuit breaker [Figure 4-1]
Circuit breaker
．．．．．．．
CAUTION
 Turn on the power of the product after turning on AC power on the back of the product
and about 10 seconds pass.
 Do not press the button of Alpha-numeric keyboard or let the button be pressed while
booting. It may cause the system malfunction.
 If turning on power of the product in the state of turning it off forcefully, the system may be
turned on instantly and then off.
 This is the characteristic of Intel® PC Main Board built in the product and not the error of
the system.
3) If pressing On/Off switch on the left of control panel (keyboard) of A30, it starts o
perating.

Service Manual
Power switch
The booting process is checked on LCD monitor and as Window XP logo

disappears, A30 logo and loading bar appear.
The loading bar is filled with a color and this time shows the process that the
software moves data into Front End Part and Back End Part of the system.
If the software data moving process is done, 2D screen appears and A30 is ready
for use.

4.3 Monitor
It is color LCD monitor and represents ultrasound image and other information.
4.3.1 Screen configuration

The screen of this product is composed of contents such as ultrasound imaging,
variousinformation and menu etc. for users to operate the system. The screen is
largelycomposed of ① title ② measurement menu ③ imaging ④ Thumbnail ⑤
User Informationetc. as follows.
[Figure 4-3] Screen configuration
① Title area
Patient information, hospital name and diagnostic subject, Frame Rate, depth,
probe information, Acoustic Output information, date and time etc. are displayed.
② Preview and measurement menu area
It shows Thumbnail imaging with preview. Measurement menu appears while
measuring diagnostic subject.
③ Imaging area
Ultrasound imaging appears. Also, imaging information,
Annotation, various measurements etc. are displayed.
④ Thumbnail area
Images saved by pressing [Acquire] button are displayed. If clicking with a pointer,
enlarged image is shown in the image area. Up to 9 images are shown.

Service Manual
⑤ User Information area

A variety of information required while a user uses this system is displayed.
The current state of the system, imaging information, possible selections etc.
are displaced.
※ Tips! Current state display of the system
: LAN connection state is displayed.

4.4 Control panel
A user can operate the system through control panel. Control panel is composed
as follows.
[Figure 4-4] Control panel
Control panel is composed of keyboard, soft menu, buttons, dial-button, slide,

track. Dial-Button is an opeartion tool combining dial and button funtions.
4.4.1 Detailed functions of control panel

The following is description and use methods of various controls in control panel.
After Chapter 3, this manual covers controls with several functions in detail.
On/Off Button Turns on/off product power
Selects patient ID in the list or Patient Information

ID Button screen where new patient information can be entered
appears

Service Manual
Probe Selection screen where probe and diagnostic

Probe Button
subject can be selected and changed appears.
The menu that can select and change diagnostic subject

Preset Button
and preset appears on the software screen.
Finishes Exam of patients being diagnosed and

End Exam Button
resets related data
The report screen organizing and showing

Report Button
measurements etc. of the diagnostic subject appears
Protocol Button Protocol Screen to use Stress Echo appears.
TM
Review Button SONOVIEW , Image Filing program, runs.
[Depth] or [Focus] function is selected and used. The

function of the button is changed every time you press the
button. The default state is [Depth].
Depth / Focus Dial-button
Depth: adjusts the depth of image that can be observed.
Focus: moves the position of focus to the target part to be

observed.
Zoom Box appears.

Zoom Dial
Press [Exit] button to exit Zoom mode.
Baseline Dial Adjusts Baseline in Doppler mode
Adjusts frequency range or velocity of blood flow

Scale Dial
in Doppler mode
Adjusts the angle of sample volume in spectral

Angle Dial Doppler mode. Also, it is used to adjust the angle of
Indicator or the probe angle of body marker.
Pointer Button The arrow-shaped pointer appears on the screen
Uses Quick Scan function. ‘Q Scan’ mark is displayed

Q Scan Button at the top of image. It can be used only in particular
diagnostic subjects of particular probe.
Acquire Button Saves images or report of screen in database

Records the images of the screen with VCR connected to
Record Button
the system
Prints the images of screen in the printer connected to

Print Button
the system
Stops images being scanned or activates stopped

Freeze Button
images again.
Starts or closes power Doppler mode.

PD Dial-button
You can adjust Gain by turning Dial-button.
Starts or closes TDI mode.

TDI Dial-button
You can adjust Gain by turning Dial-button
Starts or closes color Doppler mode.

Color Dial-button
Starts 2D mode.
2D Dial-button
Starts or closes PW spectral Doppler mode.

PW Dial-button
Starts or closes CW spectral Doppler mode
CW Dial-button You can adjust Gain by turning Dial-button
Only can be used in Phased Array probe or Static CW probe.
Starts or closes M mode.

M Dial-button
Used by setting as [Set] or [Exit] function.
- Set: Selects an item or value specified by using

Set / Exit Button trackball. Or changes the function of trackball.
- Exit: Closes the current function and returns to the

previous state
Trace Button Starts [Trace] function of basic measurements
Starts basic measurement such as distance,

Caliper Button
volume, circumference and area etc.
If pressing this button in spectral Doppler mode, D only
Update Button mode is started. If pressing this button while measuring the
distance, you can change start point or end point.

Service Manual
Deletes text, Indicator, Body Marker, measurements

Clear Button
etc. displayed on images
Calculator Button Starts measurement by diagnostic subject
Moves the cursor on the screen. Also, it has the

Trackball Trackball function such as searching for images etc. in Cine
image.
Adjusts TGC value by depth by using 8 slides.

TGC Slide
TGC stands for Time Gain Compensation.
．．．．．．．
CAUTION
• If Gain value difference of adjacent TGC Slide is adjusted greatly, lines may
occur on images.
4.4.2 Key Board

This is used to enter text etc.
[Figure 4-5] Keyboard
4.4.3 Touch-Screen
This is the operation tool that users touch directly. The function that can be used in
the mode you are currently using appears in the form of button or dial button.
- Screen configuration of touch screen
1. Information area: The title of touch screen being currently used is displayed.
2. Tab area: Diagnostic mode, Utility etc. are classified and displayed. You can
change the screen of touch screen by pressing tab.

3. Menu area: Menus that can be used in the current input mode are played in
the form of buttons. You can use it by directly pressing buttons and the menu
being used isdisplayed in orange.
4. Soft menu area: Soft menus that can be used in the current input mode are
displayed.
The menu being used is displayed in orange frame. Use it by pressing dial-
button which is right below the menu or rotating it from side to side.
．．．．．．．．．．．．．．．．．．．．．．．．．．．．．．．．．．．

※Tip! If there are two touch-screen menus
• If two menus appear at top and bottom, you can select the menu you want by
pressing the dial-button. Or press the button of menu you want to use on the
touch screen and then use dial-button.
[Figure 4-6] Touch screen

Service Manual
4.4.4 Adjustment of control panel

．．．．．．．
CAUTION
• Do not move control panel forcefully.
• Use the handle on the back of console when moving the product.
4.4.4.1 Horizontal adjustment

Hold the handle of control panel and move it from side to side carefully.
4.4.4.2 Vertical adjustment
Move the product up and down carefully pressing the lever on the handle of
control panel.

4.5 Performance checking
Chapter 4 describes the contents checking if important functions and power etc.
are operating normally after installing A30.
4.5.1 Basic checking

1) Monitor
Check Focus, Dot, afterimage, stain, spread, color of screen etc..
Check signal when shaking cable from side to side and screen status when
applying impact to Monitor
2) Control panel and LED status
Check if letters are broken or appear when pressing control panel.
Check if Keyboard LED turns on.
3) Body Mark Key
Check if Body Mark is broken or selection light operates.
4) Indicator Key
Check if trackball works smoothly when adjusting it horizontally and vertically.
5) Clear Key
Check if Text or Measure etc. is erased well.
6) Zoom operation test
Check Zoom operation and whether there is a problem.
7) Sono view test
Save each mode image and Cine Image.
Check whether there is a problem in saving images.
Check if Backup & Restore operate.
8) Measure
Check operation of Distance, Caliper, Calc etc.
9) Patient
Enter the contents in Patient and check if the same Patient value appears in
Report or SonoView etc.
10) End Exam
Measure randomly in New Patient and then check if measurement is erased when
conducting End Exam.

Service Manual
11) Probe Key

Check the operation when changing probe.
4.5.1 Detailed checking

1) B Mode
① Check whether the lines of image are missing with Knife Test.
② Check if images are abnormal or not with Phantom.
③ Check Freeze Cine related operation (Image breaking, Auto run, Auto run
Speed, Track ball Cine)
④ Check if the brightness of images changes when adjusting Gain.
⑤ Check whether to operate to see if the brightness of images changes
according to the depth when adjusting TGC Gain.
⑥ Check if images change horizontally and vertically and the direction changes
when Left/Right Flip, Up/Down Direction, Rotation is operated.
⑦ Check whether image selection menu (EE, DR, View Area, Tissue, Frame
Rate) operates.
⑧ Check whether frequency (Phantom, Res, Pen, Gen) is abnormal.
⑨ Check whether there is abnormality to see if images change depending on
depth variation.
⑩ Check whether there is abnormality to see if images change by depth when
changing focus.
⑪ Check whether image compensation mode (FSI, Harmonic, DMR, SRF, Quick
Scan, Spatial Compound Imaging) etc. operate.
2) Dual Mode
① Check whether images are abnormal with Phantom.
② Check if images change horizontally and vertically and the direction changes
③ Check image selection menu (EE, DR, View Area, Tissue, Frame Rate, Power)
related operation.
④ Check whether frequency (Phantom, Res, Pen, Gen) is abnormal.
⑤ Check whether there is abnormality to see if images change depending on
depth variation.
⑥ Check whether there is abnormality to see if images change by depth when
changing focus.

⑦ Check whether left and right image Cine (number of pages, Cine progress
order, Image breaking, Auto run, Auto run Speed, Track ball Cine) related
operation is abnormal.
3) M Mode
② Check if information of M-Line is shown on the image area.
③ Check if the brightness of images changes when adjusting Gain.
④ Check if images change horizontally and vertically and the direction changes
⑤ Check image selection menu (EE, DR, View Area, Tissue, Frame Rate, Sane
angle, Power) related operation.
⑥ Check whether there is abnormality to see if images change depending on
depth variation.
⑦ Check whether there is abnormality to see if images change by depth when
changing focus.
⑧ Check whether there is abnormality of information and speed changes
depending on speed conversion steps.
⑨ Check if image is inverted when Negative operates.
⑩ Check whether there is abnormality of Side by Side Format Image and Top
Down Format when selecting Loop Format.
⑪ Check whether there is abnormality to see if Format B-Mode and M Line area
size changes.
⑫ Check Freeze Cine (Image breaking, Auto run, Auto run Speed, Track ball
Cine) related operation.
4) C Mode & PD Mode
② Check image selection menu (Balance, Sensitivity, Color Mode, Display, CFR)
related operation
③ Check whether there is abnormality to see if images change depending on
depth variation.
④ Check Freeze Cine (Image breaking, Auto run, Auto run Speed, Track ball
Cine) related operation.
⑤ Check if the brightness of images changes when adjusting Color Gain.
⑥ When moving ROI Box, check whether there is abnormality to see if noise or
breaking problem occurs in images (B or C Mode Noise).
⑦ When adjusting ROI Box size check whether there is abnormality to see if

Service Manual
noise or breaking problem occurs in images (B or C Mode Noise).

⑧ Check if the velocity range of blood flow and conversion of frequency by
adjusting Scale vertically are adjusted (directly checking by scan).
⑨ Check if small signals are removed step by step by operating Filter.
⑩ Check if Color Bar is inverted when operating Invert key.
⑪ Check if the velocity range of blood flow moves to “+” or “-“ part by operating
Baseline vertically.
5) D Mode
② Check whether there is abnormality to see if PRF value of Doppler changes
depending on Simultaneous on/off.
③ Check whether Doppler spectrum is abnormal.
④ Check the change of velocity range by changing Scale.
⑤ Check if the range of spectrum moves to “+” or “-“ part by operating Baseline
vertically.
⑥ Check if low signal of Spectrum is changed when changing Filter.
⑦ Check if Doppler waveform is inverted when invert is operating.
⑧ Angle operates.
⑨ Change Size and the position of SV and check whether there is abnormality.
⑩ Check the image of Spectrum is changed depending on type variation
of Spectrum.
⑪ Check whether Sound Volume is abnormal.
⑫ Check if line is displayed without disconnection when Auto Calc is running and
check whether the resulting calculation values are operating automatically.
⑬ Check whether Side by Side Format Image and Top Down Format are
abnormal when selecting Loop Format.
⑭ Check Cine/Loop (Image breaking, Auto run, Auto run Speed, Track ball Cine)
related operation.
6) 3D Mode
① Check if loading is normal when skipping to Freeze and progressing with Free
Hand 3D SCAN and check whether there is noise or breaking of images during
progress.
② Check if loading is normal when progressing Static 3D Scan and whether there
is noise or breaking of images during progress. Check if Probe noise and
motor operation of probe are normal.

③ Check if loading is normal when progressing Live 3D Scan and whether there
is noise or breaking of images during progress. Check if Probe noise and
motor operation of probe are normal.
④ Check whether ROI 3D, ABC 3D, Full image is abnormal.
⑤ Check if changed to the selected angle of 3D image
⑥ Check if light and shade of 3D image is changed depending on selected
values.
⑦ Check whether images are abnormal when changing image size.
⑧ Check Display Format Image (ACB, Volume CT Image).
⑨ Select Step Angle, Rotation Angle, Rot. Axis and then check if Cine Loading is
done as items set when progressing Cine and check whether images are
broken or abnormal while Cine is operating.

Chapter 5
Product structure
Service Manual
Chapter 5 Product structure
5.1 Overview
Chapter 5 describes the behavior principle and internal structure of A30. You must read
this for maintenance and upgrade of the product. A30 is the ultrasound imaging diagnotor
to which Software DSC is applied. 21.5 inch LCD monitor was selected and high-
resolution ultrasound imaging as well as premium functions is included. To improve the
processing speed, Samsung Medison’s own new technology realized interface of the
ultrasound system and PC with the latest specifications. Improvement in processor speed
reduces the treatment time of users by speeding up processing speed. A30 can use up to
192 Element Probe and applied Digital Beam forming way of TX 128 Channel. Ultrasound
signals show ultrasound images in the LCD monitor through Front End Part and Back End
part (including PC Part). The resolution of LCD monitor is 1280 X 1024 and provides
the image formats of various shapes. There is no inconvenience while diagnosing images
due to large viewing angle of LCD panel. Also, the arm shaped monitor adjustment device
enables users to freely adjust it in varying degrees. By placing DVD RW Drive and USB
Port on the front of the product, we made Image Backup and software service convenient.
The convenient Upgrade environment is provided because you can variously use external
storage devices such as USB MO와 USB Flash Memory and external USB HDD etc.
The representative structures of A30 are as follows.
• Ultrasound System Part : PSA, AC Board , BF Board, CW Board, PCC Board,
DC to DC Power Module
• PC Part : VGA, Com-Express PC Module, Rear Board
• User Interface Part : LCD Monitor, Control Panel, Touch Panel, Track Ball,
Alphanumeric Keyboard.
• AC to DC Power Module
Chapter 5 Product structure 5-1

Contents
5.1 Overview .................................................................................................................. 5-1

5.2 System Block Diagram ........................................................................................... 5-3
5.3 Basic structure of ACCUVIX A30G ....................................................................... 5-4
5.3.1 Overview .................................................................................................... 5-4
5.3.2 Ultrasound System Part ........................................................................... 5-4
5.3.3 PC Part ...................................................................................................... 5-5
5.3.4 User Interface Part.................................................................................... 5-5
5.3.5 AC to DC Power Module ......................................................................... 5-5
5.4 PSA ........................................................................................................................... 5-6
5.5 Beam former Board................................................................................................. 5-8
5.6 CW Board............................................................................................................... 5-11
5.7 PC Carrier Board ................................................................................................... 5-14
5.8 PC Module ............................................................................................................. 5-22
5.12 Software DSC ........................................................................................................ 5-23
5.13 Rear Board............................................................................................................. 5-25
5.14 Control Panel ......................................................................................................... 5-27
5.15 Analog Control Board ........................................................................................... 5-30
5.16 Power Supply......................................................................................................... 5-31

Service Manual
5.2 System Block Diagram
[Figure 5-1] A30 System Block Diagram

5.3 Basic structure of ACCUVIX
5.3.1 Overview
A30 is composed of Ultrasound System Part, PC Part, User Interface Part and Power Part.
However, in terms of electronic structure, it can be divided into Front End Part and Back
End Part, User Interface Part, Power Part. The following is explanation on A30
of electronic structure. Front End Part is composed of AC(Analog Control),CW(Continuous
Wave) Board of Ultrasound System Part and PSA(Probe Select Assembly), BF(Beam
former) Board. The important behaviors of Front End Part are to generate by passing High
Voltage Pulse to probe and process Digital Beam forming by amplifying returned echo
signal. RF signal generated here is passed to Back End Part. Back End Part means
BE(Back End) Board and PC Part of Ultrasound System Part.
RF signal made in BF(Beam former) Board is made into various diagnostic images such
as BW, Color Doppler, PW Doppler, CW Doppler, Power Doppler etc. and displayed on
the monitor for users to see. Also, various diagnoses are possible by applying new
technologies such as SCI, DMR, AIO etc. User Interface Part means LCD monitor and
control panel (including touch panel). Power Part is divided into AC-DC Power Module and
DC-DC Power Module and AC-DC Power Module plays a role of supplying power to DC-
DC Power Module by converting AC voltage to DC voltage and supplying power to PC
Power of PC Part. DC-DC Power Module supplies voltage to Boards of Ultrasound
System Part and PC Power plays a role of supplying voltage of PC Part.
5.3.2 Ultrasound System Part

The main function is to process ultrasound data to the previous step of Scan converter.
It performs some functions of Front End Part and Back End Part
It recognizes probe and passes Application information and system information depending
on your environment to each board. Based on this information, TX Focusing and RX
Focusing are made and if passing high voltage Pulse to probe in TX Focusing process,
ultrasound waves are generated and echo signal returned from the body processes Digital
Beam forming through amplification circuit.
RF signal obtained here makes imaging signals such as BW, Color Doppler, PW Doppler,
CW Doppler, Power Doppler etc. through a variety of Filtering and Processing and is
passed to PC Part to monitor implementation. DC to DC Power Module supplies power to
Ultrasound System Part. Configuration of Ultrasound System Part is as follows.
• CW (Continuous Wave Board)
• PSA(Probe Select Assembly)

Service Manual
• AC(Analog Control)
• BF(Beam former Board)
• PCC(PC Carrier Board)
• DDM(DC to DC Power Module)
5.3.3 PC Part
The main function is composed of Scan Converter and image output circuit to display
ultrasound information made in Ultrasound System Part on the monitor. Also, it interface
between PC and Control panel. Ultrasound image information output in Ultrasound
System Part is connected from PCC to PC via DMA and implements ultrasound image
through software DSC and the existing video ultrasound imaging diagnostor
used Hardware DSC way but A30 implemented with Software DSC and shows ultrasound
image in LCD monitor. PC Power Supply uses Micro ATX as the standard and supplies
power to PC Part. Configuration of PC Part is as follows.
• PC : Com-Express PC (Samsung Embeded PC)

• CPU : Intel Core i7-3635QM
• RAM : DDR3 8GB Memory
• SDD : SATA HDD 500GB
• OS : WES(Windows Embedded Standard) 7
• VGA : General VGA Card(Nvidia GTX650)
• Monitor : 21.5” Full-HD(1924 Ⅹ1080) LED Display
• DVD
5.3.4 User Interface Part

You can diagnose ultrasound image in LCD monitor and operate A30 with control panel
and touch panel. Images output in PC Part are transmitted to LCD monitor and external
devices. Output images are VHS, S-VHS, Composite, DVI, VGA etc. and input images
are VHS, S-VHS. Also, control panel constructs various interface and users can operate
devices easily. Configuration of User Interface Part is as follows.
• LCD Monitor
• Control Panel Board
• Touch Panel
• Track Ball
• Alpha-Numeric Key Board

5.3.5 AC to DC Power Module
It converts 110/230V AC voltage coming from outside into DC voltage and then supplies it
to DDM (DC to DC Power Module) of Ultrasound System Part and supplies stabilized AC
voltage to PC Power Supply of PC Part. A power circuit breaker blocks problems caused
by overcurrent in advance.

Service Manual
5.4 PSA
5.4.1 Main function

PSA performs the functions needed to Interface System and Probe. Probe Connector has
4 260-pin Cannon Connectors and 1 LEMO Connector and HV mux is included to support
192element probe. For CW support, CW selection relay is included and in addition, each
pin is defined for 3D Probe Drive Path, Probe Insert Path, Port Select Path, CW Path,
Personality signal of probe etc. To select one from 4 probes, it is composed of Relay circuit.
5.4.2 Block Diagram
PROBE
VP_ VARA, VN_ VARA

+ HVF, - HVF
EL0~ 192
BF HV SW PROBE
Group
CONN
TX0~63 B
HV DATA[7..0]
/ HV LD
HV CLK BUFFER
MOTOR CONTROL , HALL SENSOR, XD[7..0],

XLD, XCLK, SNS[3..1] , +10REF, +HV, -HV
PROBE
CWRX0~28
H_EL163~ 191
C
EL163~ 191
CW H_EL0~28
CWTX0~28
CONN
PROBE
EL0~28
D
PRB_ SEL
PCWRX
STATIC CW
PCWTX PROBE
CWID0~3
[Figure 5-2] PSA Block Diagram
5.4.3 Specification
• 128 Channel BF Board Support
• 32 Channel CW Board Support
• 260 Pin Array Probe Connector 3ea
• Static CW Probe Connector 1ea
• High Voltage Switching (128 Channel : 192 Element)
• Probe Switching (from CW)
• Probe ID Reader (to CW)
• Board Version Reader

5.4.4 Principle of behavior
5.4.4.1 High Voltage Switching Process

A30 supports 128 Channel and uses up to 192 Element Probe. Since Pulser and
Receiver circuit configuration of BF(Beam former Board) exists only in 128
Channel, separate Element Selection is required. Element Selection uses 24 High Voltage
Switches and performs Switching with Control Signal transmitted from Control
Logic(CPLD) of BF(Beam former Board). Control Signal is connected through Mother
Board Connector. Inside of High Voltage Switch is composed of Shift Register and High
Voltage FET.
5.4.4.2 Probe Switching

It consists of the circuit to select one from 4 probes. It can select Probe ordered by User by
using Relay of Latched type. Relay is driven by Probe Select signal transmitted from
Control Logic(CPLD) of CW(Continuous Wave Board). Probe Select signal is connected
through Mother Board Connector.
5.4.4.3 CW Probe Switching

Steered CW switching
Since Steered CW has Tx 40CH and Rx 40CH separately from Beam former Board, it
converts signal line from Phased Array Probe into CW Board when steering CW Mode by
using Not latch Relay. Because it is 40CH, there are 20 AGN20012 for CW Tx and 20
AGN20012 are equipped for CW Rx.
Static CW switching
Separately from Beam former Board, Static CW has Tx 1CH and Rx 1CH. In Static CW
Mode, signal line from Pencil Probe is directly connected to CW board without Relay.

Service Manual
5.5 Beam former Board
5.5.1 Main function

A30 has 2 Beam former Boards (hereinafter called as BF Board) and implements Active
aperture of 128 Channel. BF Board generates ultrasound waves by passing High Voltage
Pulse to probe and performs even Digital Beam forming by amplifying returned echo
signal. To construct Active aperture 128 Channel, it is composed of TX Pulser circuit and
Receiving circuit and Beam former ASIC(MCB124) and performs functions such as
Dynamic Apodization, Multi Beam Receiving, TGC etc. to improve ultrasound imaging.
5.5.2 Block Diagram
MS114 Front-End Flow Path Diagam

+1.8VD +1.2V +3.3VD
+1.8VA
MAX2034 MAX2037 +1.2V +3.3VD +2.5V
LNA VGA ADC
+5VA +5VA ADS5282 FPGA

+3.3VC
+HV +11.5V +3.3VC MCB124
+3.3VD
PULSER Latch
CPLD
MAX4811(2Ch
-HV -11.5V Pulser)
+5V_REF -5V_REF +11.5V -11.5V +3.3VC +3.3VD
Controller
Analog Clock
Reference Memory
Driver Driver
Buffer
[Figure 5-3] Front End Block Diagram
5.5.3 Specification
• TX Pulser 64ea (MAX4811 : 2channel)
• Limiter 64ea
• TGC Amp 16ea (4 channel)
• AD converter 8ea (16 channel)
• BF ASIC 4ea (MCB124)
• RX Dynamic Aperture function
• RX Apodization function
• Board version Reader

• BFIC behavior can be controlled
• PSA Probe Selecting function
• Synthetic Aperture support
• Trapezoidal imaging support
• Multi-line receiving support
• TX Focal point support
5.5.4.1 TX Pulser
Exciting pulse data provided in BF ASIC(MCB124) passes TX Pulse Buffer and then is
provided to TX Pulser(MAX4811). TX Pulser creates Bipolar Pulse by using Exciting pulse
data and High Voltage provided in DC-DC Power Module. Bipolar Pulse generates
ultrasound waves by being transmitted to Probe Element by using PSA (Probe Select
Assembly). Supporting up to 192Element with Active aperture 128 Channel, separate
Element Selection is needed and High Voltage Switch is used for this. High Voltage Switch
is configured in PSA(Probe Select Assembly).
5.5.4.2 Receive Channel

Receive Channel conducts the function of conversing Analog Digital with the part Beam
forming by amplifying Echo that is spread from human medium and reflected. It consists of
Limiter, Pre-Amp, TGC-Amp, Low-Pass Filter and A/D Converter.
1) Limiter
It removes unnecessary signals from Echo signals returned through High Voltage Switch
of PSA(Probe Select Assembly). Tx Pulse of up to 180 Vpp and Echo signal of a few mV
are mixed and RX data actually needed is Echo signal of a few mV which is very small
signal so Tx Pulse should be removed before sending it to Pre-Amp. After removing about
0.6V or more of signal, Limiter sends Echo signal to Pre-Amp.
2) Pre-Amp
Pre-Amp plays a role of amplifying Echo signal of a few mV which is untreated small
signal.
3) TGC-Amp
TGC(Time Gain Compensation) Amp is composed of 4 Channel per 1. Echo signal
spread and reflected in the medium has the characteristic of attenuating depending
on time or distance and it conducts the function to compensate it.
4) Anti-aliasing Filter (Low Pass Filter)

Service Manual
Low-Pass Filter filters Noise in Stop Band not bandwidth of ultrasound signal. It also plays
a role as Anti-aliasing Filter minimizing Aliasing phenomenon that may result from high-
frequency Probe such as 7.5MHz Probe etc. Aliasing phenomenon of high-
frequency Probe occurs due to limitation of Sampling Clock in BF ASIC.
5) A/D Converter
It plays a role of converting digital signal to be used in Digital Beam forming from analog.
5.5.4.3 Digital Beam forming

Ultrasound waves generated in Probe select Channel approach using several Elements
for TX Focusing. Ultrasound waves generated in Channel unit return as Echo signal
spread and reflected in the medium. However, since Echo is Probe Element and is not
returned at the same time, it comes back with time difference to each Element and the
way to compensate this time difference is required. The reason is for RX Focusing and it is
also very important part to configure ultrasound image. Digital Beam forming conducts
sampling for Data of the place where time axis and curve meet and Echo signal entered to
Probe Element and saves it in Memory. Data accumulated in Memory after Sampling is
finished means that when it is stored, time compensation is also finished and time
compensation is made in Sampling Clock itself. RX Focusing is finished only if reading
stored data in Memory and adding it. Since this way requires different Sampling Clock for
every Element, VSCG(Variable Sampling Clock Generator) is required. VSCG(Variable
Sampling Clock Generator) uses 61.6Mhz the same as A/D Sampling Clock and
necessary Data is made inside of BF ASIC(MCB124A).

5.6 CW Board
5.6.1 Main function

CW(Continuous Wave Board) is divided into CW Board including the function of
Continuous Wave Doppler and Non CW Board without the function of Continuous Wave
Doppler. Continuous Wave Doppler function is Option and in case of the product with Non-
CW, Board should be replaced. The function of Non-CW(Continuous Wave Board) is to
provide System Clock Drive and provide Beam former Sensing and High Voltage Sensing
function and PSA related signal.
5.6.2 Block Diagram
LTX0~28
To Probe
TX Pulser TX0~28
MAX4811 Latch 0
(0~15) /LTX0~28 /TX0~28
29 L_LO
Master Clock
LO Buffer LO Drive excepting
Delay Line CW TX/RX
Current BPF
Probe LNA 32x16
Buffer
(0~1)
(0~2)
MAX2034 X-point TX0~28
(0~15)
(0~3) Switch 30nS Tab
Selection Mixer Mixer
MT8816 Max.
29 X4.7
29 (0~3)
16 I/V Ratio = 16 450nS
by TX Drive (I/Q) /TX0~28 Master Clock
27.1mV/V Frequency for CW TX/RX
X3 X1/2 LO
FPGA
BPF 1st HPF 2nd HPF ADC
I LPF ADC
50Hz~50KHz Fc = 1K or Fc = Buffer
Fc = 24bit
200Hz 400Hz Fc =
48KHz Fs =
X9.3 100KHz
X1 137.5KHz
X5.7 X1.7 X3
BPF 1st HPF 2nd HPF ADC

Q LPF ADC
50Hz~50KHz Fc = 1K or Fc = Buffer
Fc = 24bit
200Hz 400Hz Fc =
48KHz Fs =
X9.3 100KHz
X1 137.5KHz
X5.7 X1.7 X3
[Figure 5-4] CW Board Block Diagram
5.6.3 Specification
• Master Clock : System Clock Drive
• Beam former Sensing
Beam former High Voltage(+) Sense
Beam former High Voltage(-) Sense
Beam former High Current(+) Sense
Beam former High Current(-) Sense
Beam former TX Control

Service Manual
• PSA-related
Probe ID Read
Probe Insert Check
Probe Port Select
• Continuous Wave Doppler (CW Option)
Static CW Doppler TX/RX
Steered CW Doppler TX/RX
• CW Sensing (CW Option)
CW TX Voltage Sense
CW TX Current Sense
CW TX Control (CW Option)
5.6.4.1 Master Clock

Each Board is synchronized by providing 61.6Mhz, Master Clock of Ultrasound System
Part, as CW(Continuous Wave Board), BF(Beam former Board) and BE(Back End Board).
5.6.4.2 Beam former Sensing

Beam former Sensing conducts the function controlling TX voltage and TX current of
BF(Beam forming Board) and this function is performed in CPLD.
1) If voltage of TX Pulser used in Beam former High Voltage(+) Sense and Beam
former High Voltage(-) Sense BF(Beam former Board) does not meet certain
criteria, System is stopped with Error Message.
2) If current of TX Pulser used in Beam former High Current(-)Sense BF(Beam
former Board) and Beam former High Current(+) Sense does not meet certain
criteria, System is stopped with Error Message.
5.6.4.3 Beam former TX Control

It is the function controlling the intensity of voltage of TX Pulser of BF(Beam former Board)
and is performs in CPLD.
5.6.4.4 PSA-related
Performed in PSA related control function CPLD.

1) Probe ID Read
You can read Probe ID from PSA(Probe Select Assembly) and check
information on Probe.
2) Probe Inset Check
You can check whether Probe was equipped from PSA(Probe Select
Assembly).
3) Probe Port Select
If a command to select Probe connected to PSA(Probe Select Assembly) is
given, probe is selected according to Probe Select signal.
˙O
N ˙T
˙E˙
• “5.6.4.1 ~ 5.6.4.4” described Non-CW(Continuous Wave Board). Continuous

Wave Doppler function is the function added to CW(Continuous Wave Board).
5.6.4.5 Continuous Wave Doppler

Continuous Wave Doppler is the function that can detect Doppler signal of the area that
cannot be detected in Pulse Wave Doppler by continuously processing TX and RX. A30
performs this function in CW(Continuous Wave Board) and configures the circuit of
Steered CW and Static CW.
1) Static CW Doppler circuit (TX/RX 1Channel)
CW Pulser driving probe
RF Pre-Amplifier to receive signals
Mixer to convert to quadrature phase (0 degree, 90 degrees) Base-bend signal
of 50KHz bandwidth from RF signal
Thump filter
Variable Wall filter
Variable gain
Variable low pass filter
16bit analog-to-digital converters
2) Steered CW Doppler circuit (TX/RX 29 Channel)
29 Channel CW Pulser driving Probe
29 Channel RF Pre-Amplifier to receive signals
TX/RX Beam former for Focusing at the time of sending and receiving
Mixer to convert to quadrature phase (0 degree, 90 degrees) Base-bend signal
of 50KHz bandwidth from RF signal
Thump filter
Variable Wall filter
Variable gain

Service Manual
Variable low pass filter

bit analog-to-analog converters
5.6.4.6 CW Sensing
This is the function controlling TX voltage and TX current of CW(Continuous Wave).
1) CW TX Voltage Sense: If voltage of TX Pulser used in CW(Continuous Wave) does
not meet certain criteria, System is stopped with Error Message.
2) CW TX Current Sense: If current of TX Pulser used in CW(Continuous Wave) does
not meet certain criteria, System is stopped with Error Message.
5.6.4.7 CW TX Control
This is the function controlling the intensity of voltage of TX Pulser of CW(Continuous
Wave).

5.7 PC Carrier Board
5.7.1 Main function

PC Carrier Board (hereinafter called as PCC Board) is divided into DSP(Digital Signal
Processing) Part and DMA & RTC Part and Analog Sound Part. DSP Part receives RF
Data and CW I/Q Data from BF Board and CW Board, respectively and processes them
to Image Data such as BW Image, PW Doppler, CW Doppler, Color Doppler, Power
Doppler etc. Image Data made like this performs Frame Average etc. in DMA & RTC Part
of PCC Board and then, are transferred to PC Part through PCI BUS and operated by
Software DSC. Analog Sound Part processes Doppler Sound Data received in DSP Part
to Digital Analog Converter and then, transfers to Speaker by amplifying it. PCC Board is
composed of ASIC(MCB028A), FPGA, Analog Sound part etc.
[A30 V2,0 BE Board] [A30 V3.0 PCC Board ]

Service Manual
5.7.2 Block Diagram
PSA Backend
SDRAM
Data Buffer
Local PEX8311
RF(21bit), 60MHz DMA FPGA PCI Express to PCIE
Bus
Beamformer Mid. Processing Local Bus Bridge
(MCB028A) - DMA Interface
ATGC(8 or 12), 30MHz
Host PC
Seq. Control
CPLD
- Address decoding
- ETC Control
- RTC
Analog Control Seq. Control - External Trigger MID FPGA
(CW / Motor) - MCB028 Interface Doppler Sound
PC Sound
CW I/Q(24x2), 60MHz
Sound Part
SDRAM
Data Buffer
Sound I/O Board
[Figure 5-5 PCC Board Diagram]
5.7.3 Specification
• Focused RF Data Interface
• RTC(Real Time Controller)
• PCI-express Interface
• BW Data Processing
• Spectral Doppler Data Processing
• Color Doppler Data Processing
• Motion Data Processing
• Digital Signal Processing(Pre Processing, Post Processing)
• Direct Memory Access
• Sound Control(Doppler, PC Wave)

5.7.4 Principle of behavior of DSP Part
5.7.4.1 Image Data processing of BW mode and M mode

RF Data made in BF Board is entered to FPGA Input. Entered RF Data is converted to RF
Data that operation is possible in FPGA Input and then, is entered to ASIC(MCB028A)
Input. ASIC(MCB028A) makes BW mode Image Data(hereinafter BW Data) and sends it
to FPGA. ASIC(MCB028A) not only make BW Data but treats the functions such as
FSI(Full Spectrum Image) and Spatial Compound Imaging (SCI), Trapezoidal imaging,
Synthetic aperture etc. In particular, BW Data is made by receiving RF Data and through
several filters and DTGC(Digital Time Gain Compensation), Decimation, Quadrature mixer,
Envelope detection, Log compression etc. Like this, BW Data made in ASIC(MCB028A) is
entered again to FPGA. Going through Lateral filter to remove Multi beam artifact and
FSI(Full Spectrum Image) processing, final BW Data is transferred to FPGA. For reference,
BW Data can be also used as Motion mode Image Data.
5.7.4.2 Doppler Image Data processing

Data that operation is possible in FPGA and then, is entered to input of ASIC(MCB028A).
Receiving RF Data and processed with DTGC(Digital Time Gain Compensation),
Decimation, Quadrature Mixer etc., ASIC(MCB028A) is made to I/Q data (In-phase &
Quadrature Data). I/Q Data is entered again to FPGA. I/Q Data is processed in FPGA and
makes Doppler Data and transfers it to DMA & RTC Part. Detailed descriptions are as
follows. FPGA taking over I/Q Data processes Filtering process and CW I/Q Data from
CW Board also transfers final Doppler Data to PC Part through the same processing.
Since PW and CW cannot be processed at the same time, all commands will follow
the internal control process. After going through Clutter Filter, I/Q Data is sent to FFT(Fast
Fourier Transform) circuit to make Doppler Spectrum and Doppler Data is made by
detecting Power, Velocity, Variance components which are Doppler basic elements. Again,
it is entered to DSP FPGA and delivered to DMA & RTC Part of BE Board. After going
through Filtering process in FPGA, I/Q Data goes through Clutter Filter to remove
Wall(wall of blood vessels) Noise in Doppler DSP and then makes Doppler Sound by
processing in Hilbert transform the separation of the direction of sound.
5.7.4.3 Color Image Data processing

Data that operation is possible in ASIC(MCB028A) and then, is entered to input of
ASIC(MCB028A). Receiving RF Data and processed with DTGC(Digital Time Gain
Compensation), Decimation, Quadrature Mixer etc., ASIC(MCB028A) is made to I/Q data
(In-phase & Quadrature Data). I/Q Data is entered again to FPGA. I/Q Data is processed
in ASIC(MCB028A) and makes Color Data and transfers it to PC

Service Manual
Part. Detailed descriptions are as follows. FPGA taking over I/Q Data is transferred to
ASIC(MCB028A) to detect Color component. However, Color component includes
Wall(wall of blood vessels) Noise so it is transferred again to FPGA to go through the
processes such as Rejection, Smooth Filter, Post filter etc. Color Data is completed in
these processes and then, is delivered to DMA & RTC Part of BE Board.
5.7.5 Principle of behavior of Analog Sound Part

It processes Doppler Sound and outputs it to Speaker. Doppler Sound is made in Doppler
Part and transferred to Analog Sound Part. Doppler Sound goes through Audio Digital
Analog Converter process because Speaker receives Analog waveforms. And then, it
removes Noise and amplifies Doppler Sound to transfer to Speaker.
5.7.6 Principle of behavior of DMA & RTC Part

(FPGA including function)
DMA Part of DMA & RTC Part (Direct Memory Access & Real Time Controller Part)
temporarily saves ECG Data from ECG Module and Image Data(BW, Doppler, Color) that
Signal Processing is completed in DSP Part and transfers them to PCI of PC
Part depending on the purpose of Image Data. RTC Part is responsible for the function
determining the order of behavior and reference signal of all Image Modes and also
processes Control of Audio Digital Analog Converter.
5.7.6.1 DMA Part

DMA(Direct Memory Access) is largely divided into FA(Frame Average), DMA and ECG
In/Out Part. FA(Frame Average) processes BW, Doppler, Color Data as the mean value of
Scan line of current Frame and Scan line Data of prior Frame. And DMA saves Frame
Averaged BW, Doppler, Color Data temporarily and transfers necessary Data through PCI
BUS when there is a request from PC Part .Also, it saves ECG Data and transfers it in the
same way. Since DMA processes by using PC Part and DMA Path, it plays a very
important function in improving the function of the product.
5.7.6.2 RTC Part

RTC(Real Time Controller) is the part that makes reference signal needed
for overall system behavior in real time and controls the behavior of the system. It is
responsible for making signals of PRF(Pulse Repeat Frequency), OF(One Frame),
RP(Rate Pulse), Linotype, Scan Line etc. needed in DSP Part of BE Board and BF Board
and controlling them. Also, internally, it conducts the function to control the flow of Data in

DMA FPGA.

Service Manual
5.8 PC Module
5.8.1 Main function

PC Mother Board of A30 used commercial PC Mother Board. Existing Hardware DSC
Board and Video Manager Board are implemented in PC Part. Since DSC Part is
implemented with Software Program, performance of PC Mother Board is very important
and it is designed to be compatible with commercial PC Mother Board by considering the
subsequent Up-Grade. However, if using anything other than PC Mother Board supplied
by Samsung Medison Co., Ltd., performance of the product cannot be guaranteed.
Configuration of PC Module is as follows.
• PC : Com-Express PC (Samsung Embeded PC)
• CPU : Intel Core i7-3635QM
• RAM : DDR3 8GB Memory
• SDD : SATA HDD 500GB
• OS : WES(Windows Embedded Standard) 7
• VGA : General VGA Card(Nvidia GTX650)
• Monitor : 21.5” Full-HD(1924 Ⅹ1080) LED Display
5.8.2 Figure
[Top Side] [PC Bottom] [ VGA Card]

[Figure 5-6] PC Module]

5.9 Software DSC
5.9.1 Main function

A30 processes existing Hardware DSC to Software DSC configured with Software
Program. Image signals made in PCC Board are directly copied to PC Memory by using
DMA and processed by Program needed for ultrasound imaging and Software DSC and
implemented to monitor images through VGA Card
5.9.2 Block Diagram
Main Monitor
(1920 X 1080)
Touch Screen
(800 X 480) Sub Monitor
(1920X1080)
ADVR
(1280 X 853)
[Figure 5-7] Software DSC Block Diagram
5.9.3 Specification
• Software DSC
• Cine for 5,140 frame
• Loop Review for 8,192 lines
• Zoom
• Edge Enhancement
• Multi-Slice View
• Dynamic MR (Optional)

Service Manual
• Quick Scan
• Real-Time Auto Calculation time Doppler Auto Trace
• Free Angle M-Mode
• Post measurement
• Post image optimizing process Arbitrary M mode
• Panoramic View(to be updated)
• Help function

Image Data made in DMA Part of BE Board directly copies to PC Memory in the DMA way
by using 100 Pin Cable connected to PCI Board and Mother Board. It is saved in Cine
Memory through UC Agency Buffer and at this time, it is processed as Software
DSC and Image Save. Software DSC processes all functions that can be processed
by Hardware DSC with Program and processes DSC with Filter and Rendering and
transfers Data to VGA Card. Also, the way directly saved from Cine Memory to HDD when
saving image improved inconvenience slowly saved.

5.10 Rear Board
5.10.1 Main function

It conducts the function of In/Out Interface with external devices
5.10.2 Block Diagram
[Figure 5-8] Rear Board Block Diagram
5.10.3 Specification
• Rear Left
- DVI Patient Monitor Port(Image Only)
- BW Video Out
- Audio Line Out
- S-Video Out
- Mic In

Service Manual
• Rear Right
- DVI Patient Monitor Port(Full-HD)
- Ext. Trigger In / Out
- LAN Port
- USB Port x4(A30 6Port)0
5.10.4 Figure
[V2.0 Rear Board] [V3.0 Rear Board]

5.11 Control Panel

The function of Interface between users and System. Key Matrix Board, Touch Panel,
Alpha-Numeric Keyboard, Track Ball etc. conduct the function of User Interface.
[Figure 5-9] Control Panel Block Diagram

Service Manual
• USB Host Support
• USB Alpha Numeric Board
• USB Track Ball
• USB Key Matrix Board
• TGC Control
• Lamp Board
• Power Control Support
• Printer Remote Support
• Foot Switch Support

It is connected to Key Matrix Board, Alpha Numeric Board, Track Ball through USB HUB
and is operated depending on the user's command. Since Power Control is simply
connected with Switch in Key Matrix Board, detailed information will be described in
principle of behavior of Power Module.

5.12 Analog Control Board

Analog Control Board(hereinafter called as AC Board) is composed of BF High Voltage
monitoring Part, System clock Part and Motor Part to drive 3D Probe.
[Figure 5-10] Analog Control Board Block Diagram
• MOTOR support
• PSA Power support [ HV Mux / Relay ]
• Probe의 High Voltage MUX support
• Probe control [ ID check / Port Selection / Insert ]
• Power Monitoring support
• BF TX Voltage support [ Control / TX filtering ]
• BF ATGC Curve support
• System Clock support

Service Manual

3D Probe implements 3D Mode as Stepping Motor drives. Motor Board does Feedback
o
Control with COS waveforms and SIN with 90 phase difference from 3D Probe. 3D Probe
herein provides Null Position signal to Motor Board and Motor Board provides One Frame
signal, reference signal to acquire 3D Image, to PCC Board.
It plays a role of monitoring HV Power voltage of BF Board and transferring it to PC. ATGC
Curve is supplied to BF Board.

5.16 Power Supply - corrected
5.16.1.1 Main function

ACCUVIX X A30 is designed to operate in 90V~ 264V of input voltage. It is Free Voltage
and power conversion switch adjustment of the product is not necessary before use.
INPUT Voltage Selector is used to set power and voltage of the product and OUTPUT
Voltage Selector is used to set external devices directly supplied from the product.
AC voltage and DC voltage are output and AC voltage is used for external devices and PC
Power Supply and DC voltage is used for Power of Ultrasound System Part.
[Figure 5-11] AC-DC Power Module
5.16.1.2 Input-output voltage

1) Input voltage
Rated voltage Input frequency Allowable range
Free Voltage 47Hz ~ 63 Hz AC 90V ~ 264 V

Service Manual
2) Output voltage
Voltage
Output voltage Use range
classification
DC OUT 48VDC(45VDC~52VDC) 15A
AUX OUTLET 100~120VAC MAX 150VA
PC POWER 200~240VDC MAX 200W
5.16.2 DC to DC Power Module
5.16.2.1 Output voltage & overvoltage & overcurrent behavior level

If current flows within the range of overcurrent beyond rated input and maximum output
current, protection circuit operates and does not output any power of DDM.
Over Voltage Over Current

Protection Protection
Output NAME
RANGE RANGE
P1.3VA 1.76V ~ 2.24V 11 ~ 15A
P2.1VA 2.42V ~ 3.22V 16 ~ 24A
P3.6VA 4.18V ~ 5.32V 15 ~ 25A
P3.3VD 3.63V ~ 4.62V 6 ~ 11A
P5.3VA
6.05V ~ 7.7V 15 ~ 25A
P5.3VD
N5.5VA
6.05V ~ -7.7V 2.4 ~ 8.5A
N5.5VD
P12VA
13.2V ~ 16.8V 6 ~ 10A
P12VD
N12VA
-13.2V ~ -16.8V 2.4 ~ 8.5A
N12VA
P12VF 13.2V ~ 16.8V 1.2 ~ 2.5A
P24VM 26V ~ 30V 5 ~ 10A
±BTHV ±95V ~ ±100V Short Protection
±CTHV ±77V ~ ±84V Short Protection

±SHV ±105V ~ ±110V Short Protection
Behavior at At the case of over-current protection, all outputs shut off.
protection At the case of over-voltage protection, all outputs shut off.
5.16.3 PC Power Supply

AC 220V voltage from ADM is used as internal power of PC Part. Also, it is used as DVD
RW Drive power and LCD Monitor power through connector connected to the outside
of PC Part. PC Power Supply uses Micro ATX Power Supply.
5.16.4 Power Control

It describes the behavior flow of Power when turning On/Off. If switching on power of
Control Panel, power of PC Part is on and Power On Signal is transferred from PCI Board
and operates Ultrasound power. Likewise, if pressing Power Off Switch of Control Panel,
power of PC Part is off and Power Off Signal Signal is transferred from PCI Board and
Ultrasound power is turned off.

Chapter 6
Basic Maintenance
Service Manual
Chapter 6 Basic Maintenance
6.1 Overview
Chapter 6 describes the basic method to service ACCUVIX A30. It explains the version
method and the use method of Admin Mode(Service Mode) etc.
Contents
6.1 Overview .................................................................................................................. 6-1

6.2 System information ................................................................................................. 6-2
6.3 Windows Mode ........................................................................................................ 6-3
6.4 Version up ................................................................................................................ 6-4
6.4.1 Software version up .................................................................................. 6-4
6.4.2 Hardware version up ................................................................................ 6-5
6.5 Admin Mode............................................................................................................. 6-6
6.5.1 Admin Mode entry method ...................................................................... 6-6
6.5.2 Function of Admin Mode .......................................................................... 6-6
6.6 Addition and deletion of Option............................................................................ 6-13
6.6.1 Kinds of Option........................................................................................ 6-13
6.6.2 Registration of Option............................................................................. 6-13
6.6.3 Deletion of Option ................................................................................... 6-16
6.7 Monitor Brightness/Contrast Control…………………………………………………6-18
Chapter 6 Basic Maintenance 6-1

6.2 System information
For system information, select [Information] tab in the Setting screen. It shows the S/W version
information of the product. If pressing [Detail], you can check detailed Version related to the
product.
[Figure 6-1] Setup-Information
．．．．
NO T E
• S/W version of the above figure may be different from Version of the actual system.

Service Manual
6.3 Windows Mode

Windows Mode is the mode to change into general Windows XP desktop in the ultrasound
system and is the function needed for version up.
1) Press [***] + [***] + [***] simultaneously in the keyboard.
2) If Windows Password windows pops up, enter “**********” and press enter.
3) If start button is created at the bottom of the monitor, you can check successful entry of
Windows mode.

6.4 Version up
ACCUVIX A30 can perform version up of software and hardware. Version up is needed to
improve the performance of the product including the contents such as addition and improvement
etc. of the functions.
．．．．
NO T E
• Due to compatibility of software and hardware, if interoperability is unsuitable, problems occur
in functions and operation.
• Samsung Medison Global Service Group provides the compatibility table separately.
6.4.1 Software version up

Software version up uses the 3CD method.
3CD types are as follows:
st
1) 1 CD: OS Install
nd
2) 2 CD: Driver Install
rd
3) 3 CD: Application up-grade (Similar to Version Patch)
6.4.1.1 1st CD
st
1 CD is CD to install Windows XP Embedded(OS).
1) Prepare 1st CD provided by Samsung Medison Global Service Group.
2) Turn on the power of ACCVIX A30.
3) Insert 1 CD into the drive and then boot.
st
4) After 2 minutes, 1st CD program appears.

5) Select 1 or 2 of 1 CD (Default setting is Number1 )
st
① Partitioning And Formatting ALL:

② Deletes all Partitions, makes new Partition and formats all drives (including Back-Up, all
data stored in HDD are deleted).
③ No Partitioning, Formatting Only OS Partition: Formats only OS Drive(C:W). (D,E,F Drive
Data is not deleted.)
6) Problem during installation
① If “ Network ID “ input message appears, select “OK” or “Cancel” then installation goes on.
② Sometimes if Track-Ball or Key-Board is not recognized, turn Off/On the product again.
7) After installing by selecting No. 1,2, “XP” is installed and completed and then the message

Service Manual
appears after booting.

8) If software version up is completed, reboot ACCUVIX A30.
9) When booting, check if the software of the start-up screen is version up software.
6.4.1.2 2nd CD
nd
2 CD is CD to install PC Drive.
1) Prepare 2nd CD provided by Samsung Medison Global Service Group.
2) Turn on the power of ACCUVIX A30.
3) Once system booting is completed, exit to the Windows XP desktop by using
Windows mode.
4) Exit the ultrasound program.
To exit, press “Alt + F4” key of keyboard at the same time.
nd
1) Insert 2 CD into CD/DVD-ROM drive.
nd
2) 2 CD program runs automatically.
3) Select the product and press “OK” button and then, it is installed automatically
4) If the installation is completed, the product is turned “Off” automatically.
6.4.1.3 3rd CD
rd
3 CD is CD to install Application up-grade.
rd
1) Prepare 3 CD provided by Samsung Medison Global Service Group.
2) TURN ON THE POWER OF ACCVIX A30. .
3) Once system booting is completed, exit to the Windows XP desktop by using
Windows mode.
4) Exit the ultrasound program.
To exit, press “Alt + F4” key of keyboard at the same time.
rd
1) Insert 3 CD into CD/DVD-ROM drive.
rd
2) 3 CD program runs automatically.
3) Select the product and version and press “OK” button and then, it is installed
automatically
4) If the installation is completed, the product is turned “Off” automatically.

．．．．
NO T E
• For details on software version up, see “Technical Information”.
6.4.2 Hardware version up

It means replacement and addition of hardware.
．．．．
NO T E
• For hardware version up, see the service manual “Chapter 8 disassembling and assembling”

Service Manual
6.5 Admin Mode

Admin Mode is also called as Service mode and describes the function provided herein
This is the function needed to add, delete Option and important setup.
6.5.1 Admin Mode Entry Method

1) Press [***] on the keyboard.
2) Enter “**********” and press enter.
3) If entered password is correct, “Admin Mode” Tab is created in Setup Mode.
4) If selecting “Admin Mode”, entry to Admin Mode is completed as shown in [Figure 6-2].
[Figure 6-2] Admin Mode
6.5.2 Function of Admin Mode
6.5.2.1 Language
Select the language used in the product. It can be selected through the filter and 7 kinds of
languages can be selected such as English, German, French, Spanish, Italian, Russian,
Chinese.

6.5.2.2 Test Pattern
You can test the characteristics of the monitor.
Every time you select [Test Pattern] and press [Set] button of the keyboard, you can test the
monitor with three types of Test Pattern as shown in [Figure 6-3] below.
[Figure 6-3] Test Pattern
6.5.2.3 Restore
It is the function setting backed up User settings as the product and possible only in Admin
Mode.
1) If pressing [Restore], the ultrasound program is terminated and Restore function is
started.
If asked if you want to exit the ultrasound program before starting Restore, select [OK].
2) You can select User setup Item and Backup Media in [Restore] screen.
3) If pressing [Next], Backup function is performed.
4) If Restore is completed, rebooting is conducted.

Service Manual
[Figure 6-4] Restore
[Figure 6-5] Restore running
6.5.2.4 Backup
It is the function backing up User settings to external Media and possible only in Admin Mode.
1) If pressing [Backup], the ultrasound program is terminated and Backup function is
started.
If asked if you want to exit the ultrasound program before starting Backup, select
[OK].
2) You can select User setup Item and Backup Media in [Backup] screen.
3) If pressing [Next], Backup function is performed.
4) If Backup is completed, rebooting is conducted.

[Figure 6-6] Backup
[Figure 6-7] Backup running

Service Manual
6.5.2.5 Check and Fix OS Volume

You can check whether there is physical damage to HDD Drive where OS is installed.
6.5.2.6 Network Configuration

The screen moves to Network Configuration screen of Windows XP.
Network setup such as DICOM etc. is possible.
[Figure 6-8] Network Configuration
6.5.2.7 VGA
You can select scan mode of Video Out Format: Video Out output.
It can be selected through the filter and selectable scan modes are NTSC, PAL mode.

6.5.2.8 Printer
You can adjust Printer setup. You can adjust Printer setup by using the printer shaped icon.
[Figure 6-9] Printer
6.5.2.9 CP LCD Font

You can set Font appearing on LCD screen in CP. If selecting the font of the desired type, it is
applied to CP LCD. There are total 4 kinds such as Tahoma (7), Tahoma (8), Arial (7), Arial (8).
6.5.2.10 Display Information

You can modify information appearing on the screen. There are 4 kinds such as System name,
Patient Name, Freq. Display, Ref. Physician.
1) System name
You can change logo appearing on top left of the Image screen.
Medison: displayed as Medison Logo.
SonoAce: displayed as SonoAce Logo.
Model: displayed as Model Logo.
2) Patient Name
You can select how to show patient information.
Patient + Age: displays patient’s name and age.
Patient + Birth Date: displays patient’s name and date of birth.
3) Frequency Display

Service Manual
You can determine whether to display frequency.
4) Ref. Physician
You can set Diag. Physician, Ref. Physician, Sonographer name display on the screen.

6.6 Addition and deletion of Option
It describes the process of adding and deleting Option in ACCUVIX A30.
The add and delete process of Option means Unlock / Lock way and Unlock herein means the
state to use Option arbitrarily and Lock means the state that cannot use Option. Option is
classified into software way and hardware way and you can check the contents of Option in
Setting mode.
6.6.1 Kinds of Option

You can use Option of ACCUVIX A30 by entering Option Password or mounting hardware.
Options: Display the types of option software that can be installed in this product.
Option software of ACCUVIX A30 is as follows.
4D Auto IMT
3D XI ElastoScan
CW Function Panoramic
Cardiac Measurement 3DMXI Upgrade
DICOM HDVI
Spatial Compound VolumeNT
XI STIC ADVR
Status: Displays the current state of option software.

Lock_Not Installed: Hardware is not connected
Lock_Unregisterd: Use of software is unregistered.
Lock_Installed: Installation of hardware was completed but it cannot be used.
Unlock_Permanent: Can be used without restriction during the use period
Unlock_Restricted: Can be used during the specific use period.

Service Manual
6.6.2 Registration of Option
6.6.2.1 Input Option Password

You can describe the cases registering (Unlock) Option by entering Password
1) Switched to Admin Mode. See “6.5.1. Admin
entry method”
2) The key-shaped button is activated in the
upper right corner of Option Tab. Option
Password can be entered when this button is
activated.
3) Select Option to be added and press the key-
shaped button and then enter Password.
4) If Password is correct, press [OK] button and
reboot the product.
[[Figure 6-10] Option Tab deactivation

[Figure 6-11] Option Tab activation
[[Figure 6-12] Input Option Password
6.6.2.2 Option Password registration after replacing HDD

ACCUVIX A30 was designated to maintain Option Password even though bad HDD is
replaced.
You can describe the cases entering (Unlock) Option Password by replacing HDD.

Service Manual
1) Switched to Admin Mode. See “6.5.1. Admin entry method”

2) [Change HDD] button is created in the middle part of Option Tab.
3) If pressing [Change HDD] button, Option Password of the product is entered
(Unlock).
4) Check Option Unlock and reboot the product.
[Figure 6-13] Change HDD
6.6.3 Deletion of Option

It describes the cases of deleting option.
1) Switched to Admin Mode. See “6.5.1. Admin entry method”
2) The key-shaped button is activated in the upper right corner of Option Tab. Option
Password can be deleted when this button is activated.
3) Select Option to be deleted and press the key-shaped button and then delete
Password.
4) After deleting Password, press [OK] button and reboot the product.

6.7 Monitor Brightness/Contrast
The use of Brightness/Contrast menu of the Touch Screen is impossible by the

use of Windows7 in the A30 v3.00.00. So, we can adjust as below through the
separate setting.
1) Go into the window mode after the product booting.
2) If you press [SET] button, the following screen is displayed then click “ NVIDIA
Control Panel “ in the menu
[Figure 6-14] Display Control
3) If NVDIA Control Panel is performed, select the display-> Adjust desktop color
settings item of the left menu.

Service Manual
[Figure 6-15] Desktop Color Setting

Chapter 7
Diagnosis of failure
Chapter 7 Trouble Shooting
7.1 Overview
Chapter 7 describes basic troubleshooting procedures.
˙O
N ˙T
˙E˙
 Procedures for troubleshooting expected problems are described. Unexpected
situations may occur.
 Procedures for troubleshooting normal problems are described.
7.1 Overview ............................................................................................................... 7-1

7.2 Power .................................................................................................................... 7-2
7.2.1 Power Failure ........................................................................................... 7-2
7.2.2 Power cannot be turned off..................................................................... 7-2
7.2.3 Power is automatically turned off ........................................................... 7-3
7.3 Monitor..............................................................................................................7-4
7.3.1 Blank Screen.........................................................................................7-4
7.3.2 Screen Color is Abnormal................................................................... 7-4
7.4 Error Messages……………………………………………………………….7-5
7.4.1 System hangs after an error during booting…………………………7-5
7.4.2 System works even if error occurred…………………………………7-5
7.4.3 Error code……………………………………………………………….7-5
7.5 Image……………………………………………………………………………7-6
7.5.1 No BW Image Echo7-6………………………………………………...7-6
7.5.2 No BW Mode Image Format…………………………………………..7-6
7.5.3 Noise Link Rain over the BW Mode Image (Noise)………………… 7-6
7.5.4 PW Doppler Mode Trouble…………………………………………….7-7
7.5.5 CW Doppler Mode Trouble……………………………………………7-7
7.5.6 Color Doppler Mode Trouble………………………………………….7-7
7.5.7 Motion Mode Trouble………………………………………………….7-7
Chapter7 Troubleshooting 7-1

7.2 Power
7.2.1 Power Failure

This may occur if the power cord is not properly connected or the Power Supply is not working.
1) Check if the power cord is properly connected and if the cut-off switch of the ADM is
turned on.
2) Check the fuse status.
3) Connect another device to the wall outlet and check if it works.
If the device works, there is a Power Supply problem.
If the device does not work, the problem is down to the wall outlet.
4) Check if the system fan works.
If the fan works, the problem is not a power supply problem.
If the fan does not work, a PC Power problem is likely.
5) Check if the NOR Alarm LED of ADM is on.
If the NOR LED is on, DDM is normal.
If the OVP, OLP or OTP LED is on, there is a problem with the DDM.
6) Disconnect the power cord and connect it again after 1 or 2 minutes.
7) Check the output voltage of the ADM.
The input voltage for the PC Power Supply is 110V/220V.
The input voltage for the DDM is around 24V.
If the voltage is not within the normal range, an ADM problem is likely.
8) Check the PC Power Supply and DDM.
7.2.2 Power cannot be turned off

A software error or PCC board, PC Module problem is likely.
1) The power is automatically turned off when the Power Switch is pressed for more
than 3 seconds. If software such as printer software is running or an operating
system error occurs, the power is not turned off.
2) If you cannot turn the power off after completing the procedures in PCC board, PC
Module problem is likely.
7.2.3 Power is automatically turned off

Power cord, PCC board, PC Module trouble is expected.
1) Check if the power cord is properly connected and if the cut-off switch of ADM is
turned on.
2) Check the fuse status.
3) Connect another device to the wall outlet and check if it works.
If the device works, it is due to Power Supply problem.

If the device does not work, it is due to wall outlet problem.
4) If the power is automatically turned off after completing the procedures of “ 1), 2) and 3)”
PCC Board or PC Module trouble is expected.

7.3 Monitor
7.3.1 Blank Screen

DVI Cable or VGA Cable is improperly connected or monitor or PC Part trouble is expected.
1) Try to print to check the product status.
If printing is normal, monitor or PC Part trouble is expected.
2) Check the cable is properly connected with the monitor.
Check the DVI Cable connection of the PC Part and LCD IF Board.
Check the DVI Cable connection of the LCD IF Board and monitor.
Check the DVI Cable and VGA Cable.
3) If no problem has been found in the above “1) and 2)”, monitor and PC Part trouble
is expected. Check the PC Module and VGA Card of the PC Part.
7.3.2 Screen Color is Abnormal

DVI Cable of the monitor or PC Part is improperly connected or monitor or PC Part trouble is
expected.
1) Check the monitor connection cable status.
Check the DVI Cable connection of the PC Part and LCDIF Board.
Check the DVI Cable connection of the LCDIF Board and monitor.
Check the DVI Cable and VGA Cable.
2) If no problem has been found in the above “1)”, monitor and PC Part trouble is
expected. Check the the PC Module and VGA Card of the PC Part.

7.4 Error Message
7.4.1 System hangs after an error during booting

Temporary software error or product trouble is expected.
1) Turn the power off by force and then turn it on again after 1 to 2 minutes.
2) If the symptom continues after completing “1)”, check when the error message
appears.
If the error message appears while Windows 7 is running, operating system or PC
Part trouble is expected.
If the error message appears after system logo appears, system software or
Ultrasound System Part trouble is expected.
7.4.2 System works even if an error occurred

Temporary software error or product trouble is expected.
1) Turn the power off by force and then turn it on again after 1 to 2 minutes.
2) If the symptom continues after completing “1)”, check when the error message
appears.
If the error message appears while Windows XP is running, operating system or
PC Part trouble is expected.
If the error message appears after system logo appears, system software or
Ultrasound System Part trouble is expected.

7.4.3 Error Code
Software error or Product trouble is expected. refer to `Table 7-1 Error code’.
Part Error Code Expected Trouble
0 FILE_NOT_FOUND
FILE and
1 DEMO_PERIOD_EXPIRED_ERROR
OTHERS
2 CRC32DLL_LOAD_FAIL
PC 10 PCI9054_OPENDMA_FAIL_IN_HWINIT
21 NO_MOTOR_CONTROL_FOUND
MOTOR 22 MOTOR_NULL_POSITION_LOST
Part
23 MOTOR_CONTROL_SEQUENCE_BROKEN
(AC
BOARD) 24 GAIAMOT_DLL_LOAD_ERROR
25 GAIAMOT_DLL_OLD_LOAD_ERROR
40 FPGA_DOWNLOAD_ERROR_BF
BF
163 BF_DMA_WRITE_CHECKSUM_ERROR
BE 100 FPGA_DOWNLOAD_ERROR_BE
CW 101 FPGA_DOWNLOAD_ERROR_DMA
BE 102 FPGA_DOWNLOAD_ERROR_DMA
BE 114 RTC_STOP_ERROR
Power 162 HV_HIGH
[Table 7-1] Error Code

7.5 Image
7.5.1 No BW Mode Image Echo

Probe and the system connection, BF Board or DDM trouble is expected.
1) Check the connection between the probe and the system.
2) Check if probe oscillation sound is heard.
If oscillation sound is heard, the problem may be DDM trouble.
If NOR LED is on, DDM is normal.
If OVP, OLP or OTP LED is on, the problem is DDM trouble.
4) If no problem has been found in the above “1), 2), and 3)”, BF Board trouble is
expected.
7.5.2 No BW Mode Image Format
Probe and the system connection, Ultrasound System Part or PC Part trouble is expected.
1) Check the connection between the probe and the system.
2) Check if probe oscillation sound is heard.
If oscillation sound is heard, the problem may be DDM trouble.
If NOR LED is on, DDM is normal.
If OVP, OLP or OTP LED is on, the problem is DDM trouble.
4) If no problem has been found in the above “1), 2), and 3)”, Ultrasound System Part
or PC Part trouble is expected.
7.5.3 Noise Like Rain over the BW Mode Image (Noise)
Power noise or BF Board trouble is expected.
1) Check if the system shares the wall outlet with another device.
If the system shares the wall outlet with a device that uses electric motor or
consumes high power, noise may be generated.
2) If the symptom continues when you connect the system to the wall outlet of another
room, the problem is power noise.
3) If no problem has been found in the above “1) and 2)”, BF Board trouble is
expected.
7.5.4 PW Doppler Mode Trouble
Ultrasound System trouble is expected.
1) If BW Mode is normal, BE Board trouble is expected.
2) If BW Mode has a problem, BF Board trouble is expected.
7.5.5 CW Doppler Mode Trouble
1) If PW Doppler Mode is normal, CW Board trouble is expected.
2) If PW Doppler Mode has a problem, BE Board trouble is expected.

7.5.6 Color Doppler Mode Trouble
7.5.7 Motion Mode Trouble

Chapter 8
Disassembling and assembling
Service Manual
Chapter 8 Disassembly
8.1 Overview
Chapter 8 describes the disassembling process of ACCUVIX A30.
Refer to it when repairing failure or upgrading hardware.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• Dangerous high voltage flows inside the product. Never disassemble the product.
Physical disability may be caused due to electrical shock.
• Only Samsung Medison Global Service Group or authorized engineers can repair the
product or replace parts.
• The manufacturer is not responsbible for material damages and physical disability
caused by ignoring this warning.
• If working while the product is on, do not use anti-static wristband. Physical disability may
be caused due to electrical shock.
˙O
N ˙ T˙ E˙
• When disassembling and assembling the product, use anti-static gloves and wristband.
• The industrial accidents of engineers can be prevented and defects in the product due to
static electricity can be reduced.
[Figure 8.1 Antistatic Gloves and Wrist Strap]
Chapter 8 Disassembling and assembling 8-1

Contents
8.1 Overview .................................................................................................................. 8-1

8.2 Disassembly Front Low Part ................................................................................ 8-4
8.2.1 Preparation .............................................................................................. 8-4
8.2.2 Front Low Cover ....................................................................................... 8-4
8.2.3 PSA ASSY ................................................................................................. 8-4
8.2.4 Main Board (BF, BE, CW, MTR) ............................................................. 8-4
8.2.5 ECG Module ............................................................................................ 8-5
8.3 Disassembly Rear Low Part Rear Low Part ........................................................ 8-6
8.3.1 Preparation ................................................................................................ 8-6
8.3.2 Rear Cover ASSY..................................................................................... 8-6
8.3.3 HDD .......................................................................................................... 8-9
8.3.4 DC to DC Power Module ....................................................................... 8-10
8.3.5 AC to DC Power Module ....................................................................... 8-11
8.3.6 Body Top Cover ...................................................................................... 8-12
8.3.7 Rear Fan .................................................................................................. 8-13
8.3.8 Rear Board ……………………………………………………………8-14
8.4 Disassembly User Interface Part ....................................................................... 8-15
8.4.1 Preparation ............................................................................................ 8-15
8.4.2 Control Panel ASSY ............................................................................... 8-15
8.4.3 Touch Panel............................................................................................. 8-16
8.4.4 Track Ball ................................................................................................. 8-17
8.4.5 Control Panel Board ............................................................................... 8-18
8.4.6 Alpha-Numeric Board............................................................................. 8-19
8.5 Disassembly Rear Upper Part .. .......................................................................... 8-20
8.5.1 Preparation ............................................................................................ 8-20
8.5.2 Handle AY ................................................................................................ 8-20
8.5.3 Body Arch Inner Right & Left Cover...................................................... 8-21
8.5.4 DVD .......................................................................................................... 8-22
8.5.5 Speaker Right & Left .............................................................................. 8-24
8.6 Disassembly LCD & ARM .................................................................................. 8-24
8.6.1 Preparation ............................................................................................ 8-24
8.6.2 LCD .......................................................................................................... 8-24
8.6.3 LCD ARM................................................................................................. 8-25

Service Manual
8.7 Disassembly Side Cover & Body Arch Front .................................................... 8-26
8.8.1 Preparation ............................................................................................ 8-26
8.8.2 Body Side Right & Left Cover................................................................ 8-27
8.8.3 Body Arch Front Cover........................................................................... 8-28

8.2 Disassembly Front Low Part
8.2.1 Preparation
- Prepare a (+) driver and anti-static gloves.
- Exit the product (See 3.7)
8.2.2 Front Low Cover

- Hold Front Low Cover and disassemble it in the direction of the arrow from the top.
You can disassemble Front Low Cover by holding and pulling the top of Front Low Cover
without separate Tools.

Service Manual
8.2.3 PSA ASSY

- Disassemble Front Low Cover. (See 8.2.2)
- Loosen 18 screws of PSA ASSY by using (+)a driver.
- Disassemble it by holding PSA ASSY handle with both hands and pulling it.

8.2.4 CW Board, BF Board, PCC Board, AC Board
- Disassemble Body Front Cover. (See 8.2.2)
- Disassemble PSA ASSY. (See 8.2.3)
- Disassemble it by holding the handle of CW Board with both hands and pulling it.
- Disassemble it by holding the handle of BF Board(2ea) with both hands and pulling it.
- Disassemble it by holding the handle of BE Board with both hands and pulling it.
- Disassemble it by holding the handle of MTR Board with both hands and pulling it.
[PCC Module]
[CW Board] [AC Board]
[BF Board]

Service Manual
8.2.5 ECG Module

- Loosen 1 screw of ECG module by using a (+) driver.
- Disassemble ECG Module by holing and pulling it.
- Disassemble Cable of ECG Module.
1 Screw
ECG Module

8.3 Disassembly Rear Low Part
8.3.1 Preparation
- Exit the product. (See 3.7)
8.3.2 Rear Cover ASSY

- Open Door Cover and seperate Cable connected to Rear Assy
- Remove 6 screws of Body Rear Cover by using a (+) driver.
- Hold Body Rear Cover and disassemble it in the direction of the arrow.
- Remove 4 Screws of Rear Cover and separate the rear cover.
6 Screw

Service Manual
8.3.3 HDD
- Disassemble Body Rear Cover. (See 8.3.2)
- Disassemble all cables connected to HDD.
- Loosen 4 screws by using a (+) driver and disassemble it.
Cable Connector
4 Screw

8.3.4 DC to DC Power Module
- Disassemble HDD. (See 8.3.4)
- Loosen 5 screws of DC to DC Power Module by using a (+) driver.
- Disassemble it by holding the handle of DC to DC Power Module with both hands and
pulling it.
4 Screw

Service Manual

- Separate all cables connected to AC to DC Power Module.
- Loosen 2 screws of AC to DC Power Module by using a (+) driver.
- Disassemble it by holding and pulling AC to DC Power Module.
2 Cable
2 Screw

8.3.6 Body Top Cover
- Loosen 8 screws of Body Top Cover by using a (+) driver
- Hold Body Top Cover and disassemble it in the direction of the arrow.
8 Screw

Service Manual
8.3.7 Rear Fan

- Loosen 14 screws of Rear Fan ASSY by using a (+) driver.
- Disassemble Cable of Rear Fan.
14 Screw
8 Screw
Rear Fan Cable

8.3.8 Rear Board
- Remove all cables connected to Rear Board.
- Remove 4 screws of Rear Board Cover by using a (+) driver.
- Separate Rear Board..
6 Screw

Service Manual
8.4 Disassembly of User Interface Part
8.4.1 Preparation
8.4.2 Control Panel ASSY

- Disassemble Cover of Control Panel and loosen screws by using a (+) driver.
- Loosen screws of Control Panel by using a (+) driver.
- Disassemble Cable of Control Panel Board.
- Disassemble the front panel of Control Panel.
2 Screw
12 Screw
Cable

8.4.3 Touch Panel
- Disassemble the front panel of Control Panel.(See 8.5.2)
- Disassemble all cables connected to Touch Panel.
- Loosen 5 screws of Control Panel by using a (+) driver and disassemble it.
5 Screw
6 Screw

Service Manual
8.4.4 Track Ball

- Disassemble the front panel of Control Panel. (See 8.5.2)
- Disassemble Touch Panel.(See 8.5.3)
- Disassemble Cable of Track Ball.
- Loosen 2 screws of Track Ball by using a (+) driver and disassemble it.
2 Screw
Cable

8.4.5 Control Panel Board
- Disassemble the front panel of Control Panel. (See 8.5.2)
- Disassemble Touch Panel. (See 8.5.3)
- Disassemble Track ball.(See 8.5.4)
- Disassemble Switch Cap of Control Panel.
Switch Cap
27 Screw

Service Manual
8.4.6 Alpha-Numeric Board

- Disassemble the front panel of Control Panel.(See 8.5.2)
- Disassemble KeyBoard Stopper.
- Disassemble Cable of Control Panel Board.
- Loosen 6 screws of Alpha-Numerical Keyboard by using a (+) driver and disassemble it.
Cable
2 Screw
6 Screw

8.5 Disassembly Rear Upper Part
8.5.1 Preparation
8.5.2 Handle AY
- Loosen 11 screws of Handle AY by using a (+) driver.
- Hold Handle AY and disassemble it.

Service Manual
8.5.3 Body Arch Inner Right & Left Cover

- Disassemble Body Top Cover. (See 8.3.7)
- Disassemble Handle AY.( See 8.6.2)
- Loosen 4 screws of Body Arch Inner Right Cover and Left Cover respectively by using a
(+) driver.
- Hold Body Arch Inner Right Cover and Left Cover and disassemble them in the direction
of the arrow.
disassemble

8.5.4 DVD
- Disassemble Handle AY. (See 8.6.2)
- Disassemble Cable of DVD.
- Loosen 2 screws of DVD by using a (+) driver.
- Disassemble DVD by holding and pulling it.
2 Screw & Cable

Service Manual
8.5.5 Speaker Right & Left

- Disassemble Body Arch Inner Left Cover.(See 8.6.3)
- Disassemble Cable of Speaker.
- Loosen 2 screws of Speaker Right and Left by using a (+) driver and disassemble it.
Cable
L R
4 Screw

8.6 Disassembly LCD & ARM
8.6.1 Preparation
8.6.2 LCD
- Loosen 2 screws of Lear Back LCD Cover.
- Loosen 4 screws of LCD Panel by using a (+) driver.
- Hold LCD Panel with both hands and disassemble it.
- Disassemble Cable connected to LCD.
2 Screw 4 Screw
Cable

Service Manual
8.6.3 LCD ARM

- Disassemble DVD. (See 8.6.4)
- Disassemble Cable of LCD.
- Hold both sides of Base Lower Back Cover and disassemble it
- Loosen 2 screws of Base Lower Front Cover by using a (+) driver and disassemble it
- Loosen 4 screws of LCD ARM by using a (+) driver and disassemble it
2 Screw
4 Screw

8.7 Disassembly Side Cover & Body Arch Body
8.7.1 Preparation

Service Manual
8.7.2 Body Side Right & Left Cover

- Disassemble Body Arch Inner Right Cover and Left Cover.(See 8.6.3)
- Remove 18 screws of Body Side Right Cover and Left Cover respectively
- Disassemble by holding and pulling Cover Body Side Right and Left
18 Screw

8.7.3 Body Arch Front Cover
- Loosen 3 screws of Body Arch Front Cover by using a (+) driver
- Disassemble Body Arch Front Cover by holding it
3 Screw 3 Screw

Chapter 9 Probe
Service Manual
Chapter 9 Probe
9.1 Overview
Probe is the device obtaining image data by transferring and receiving ultrasound waves
and is also called as Transducer or Scan head. This product limits the temperature that
patients can contact to 43 degrees Celsius and ultrasound output values comply with the
limit standards of U.S. FDA. The power protection fuse of this product protects the product
from overcurrent. If power monitoring protection circuit detects overcurrent, it prevents the
probe surface from overheating by immediately blocking current connected to probe and
limits ultrasound output.
Contents
9.1 Overview .................................................................................................................. 9-1

9.2 Probe list................................................................................................................... 9-2
9.3 Thermal index table (TI Table) ............................................................................... 9-5
9.4 Use of ultrasound gel ............................................................................................ 9-6
9.5 Probe safety matters ............................................................................................... 9-7
9.6 Use of protective cover (Sheaths) ......................................................................... 9-9
9.7 Cleaning and disinfection of probe ...................................................................... 9-11
Chapter 9 Probe 9-1

9.2 Probe list
The ultrasound imaging diagnostor displays image data inside the body obtained by using
probe on the screen. To obtain the best image, use probe suitable for diagnostic subjects.
Also, it is recommended for you to set probe according to the characteristics of organs that
you want to scan.
9.2.1 Diagnostic subject and setup of probe

Setup of diagnostic subjects and kinds of probe that can be used in this product are as
follows.
Diagnostic
Probe setup
subject
Small Parts Bowel, Breast, Testicle, Thyroid
Vascular Arterial, Carotid, Venous
L4-7
Abdomen General
MSK General
Small Parts Bowel, Breast, Testicle, Thyroid
L5-13IS Vascular Arterial, Carotid, Venous
MSK Shoulder/Knee, Hand/Foot, Elbow/Wrist
Small Parts Breast, Testicle, Thyroid
L7-16IS Vascular Superficial, Carotid
MSK Shoulder/Knee, Hand/Foot, Elbow/Wrist
Abdomen Aorta, General, Renal
st nd rd
OB 1 Trimester, 2 Trimester, 3 Trimester, Fetal Echo
C1-4
Gynecology General, Adnexa
Contrast Perfusion
st nd rd
C2-6IC OB 1 Trimester, 2 Trimester, 3 Trimester, Fetal Echo
Pediatric Abdomen, Neo Head
C5-8
Vascular Carotid, Arterial, Venous
st
OB 1 Trimester
EC4-9IS Gynecology General, Adnexa
Urology Prostate
st
OB 1 Trimester
VR5-9 Gynecology Uterus, Adnexa
Urology Prostate
P2-4BA Cardiac Aortic Arch, Adult Echo, Ped Echo
TCD General
st nd rd
V2-6 OB 1 Trimester, 2 Trimester, 3 Trimester, Fetal Echo
V4-8 Abdomen Aorta, General, Renal
Chapter 9 Probe 9-2

Service Manual
Diagnostic
Probe setup
subject
st nd rd
OB 1 Trimester, 2 Trimester, 3 Trimester, Fetal Echo
st
OB 1 Trimester
V5-9 Gynecology General, Adnexa
Urology Prostate
CW2.0 Cardiac Adult Echo
CW4.0 Cardiac Adult Echo, Ped Echo
Cardiac Ped Echo
CW6.0
Vascular Arterial, Venoous
˙O
N ˙ T˙ E˙
• In addition to setup pre-optimized in the system, you can select setup that you want from
User1 ~5. For the contents on setup and selection of probe, see ‘Chapter 3. Starting
diagnosis’.
9.2.2 List of functions

The functions that can be used according to diagnostic subject and probe in this product
are as follows.
Diagnostic Elasto
Probe Har PI SCI DMR+ Q Scan ECG Biopsy
subject Scan
Small Parts O X O O O O X O
Vascular O X O O O O X O
L4-7
Abdomen O X O O O O X O
MSK O X O O O O X O
X
Small Parts O X O O O O (Except O
L5-13IS Breast)
Vascular O X O O O O X O
MSK O X O O O O X O
Small Parts O X O O O O X O
L7-16IS Vascular O X O O O O X O
MSK O X O O O O X O
Abdomen O O X O O X X O
OB O O X O O X X O
C1-4
Gynecology O O X O O X X O
Contrast O O X O O X X O
C2-6IC OB O O X O O X X O
C5-8 Pediatric X X X O O X X X
Chapter 9 Probe 9-3

Diagnostic Elasto
Probe Har PI SCI DMR+ Q Scan ECG Biopsy
subject Scan
Vascular X X X O O X X X
OB O X X O O X X O
EC4-9IS Gynecology O X X O O X O O
Urology O X X O O X O O
OB O X X O O X X O
VR5-9 Gynecology O X X O O X O O
Urology O X X O O X O O
Abdomen O O X O O X X X
P2-4BA Cardiac O O X O O O X X
TCD O O X O O X X X
V2-6 OB O O X O O X X O
V4-8 OB O O X O O X X O
OB O X X O O X X O
V5-9 Gynecology O X X O O X X O
Urology O X X O O X X O
CW2.0 Cardiac X X X X X O X X
CW4.0 Cardiac X X X X X O X X
Cardiac X X X X X O X X
CW6.0
Vascular X X X X X O X X
˙O
N ˙ T˙ E˙
• The meanings of the signs shown in the table are as follows:

- Q Scan: Quick Scan
- Har: Harmonic imaging
- PI: PuIse Inversion
- PPI: Power Pulse Inversion
- TDI: Tissue Doppler Imaging
- CM: Color M mode
- ECG: Electro Cardio Graph
Chapter 9 Probe 9-4

Service Manual
9.3 Thermal index table (TI Table)

Thermal Index (TI) is displayed in the title area of the screen and represents the possibility
of temperature rise in certain parts of the body. It is divided into body tissue thermal index
(TIs), bone thermal index (TIb), skull thermal index (TIc) depending on the part..
This product is set for thermal index to be automatically displayed according to probe and
diagnostic subjects.
See the following table.
Diagnostic subject
Contrast Agent
Gynecology
Probe
Small Parts
Obstetrics
Abdomen
Pediatric
Vascular
Urology
Cardiac
MSK
TCD
L4-7 TIs TIs TIs TIs
L5-13IS TIs TIs TIs
L7-16IS TIs TIs TIs
C1-4 TIs TIb TIs TIs
C2-6IC TIs TIb TIs
TI
C5-8 TIs
s
EC4-9IS TIb TIs TIs
VR5-9 TIb TIs TIs
P2-4BA TIs TIs TIs
V2-6 TIs TIb TIs
V4-8 TIs TIb TIs
V5-9 TIb TIs TIs
CW2.0 TIs
CW4.0 TIs
CW6.0 TIs TIs
VR5-9 TIb TIs TIs
V4-8 TIs TIb TIs
Chapter 9 Probe 9-5

9.4 Use of ultrasound gel
Inappropriate ultrasound gel may damage probe. For transmission of appropriate acoustic
signals, use only ultrasound gel recommended by Samsung Medison.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• Mineral oil, coupling medium containing oil or unauthorized substances may damage
probe so do not use them. Do not use ultrasound gel containing the following chemical
substances.
- Acetone
- Methanol
- Denatured alcohol
- Mineral oil
- Iodine
- Lanolin
- Any lotion or gel containing aromatic substances
Chapter 9 Probe 9-6

Service Manual
9.5 Probe safety matters

Probe may be easily damaged by incorrect use or contact with certain chemicals. Check
before• after use of probe, probe cable, case and lens etc. in accordance with the manual.
Check if there are cracks on probe, splitting, leakage of solution, damage by sharp corner
etc. and if damage is detected, stop using probe and contact Samsung Medison service
team. Damaged probe may cause injury such as electrical shock etc. to patients or users.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Do not apply mechanical shock to probe.

• Do not let probe cable be stepped to the wheels and do not forcefully bend or pull.
• Do not immerse probe in inappropriate materials such as alcohol, bleach, ammonium
chloride, hydrogen peroxide etc. Do not expose it to more than 50℃.
9.5.1 Operation of probe and infection control

Probe used in ultrasound imaging diagnostor is directly contacted to patients. Depending
on the type of checkup, this kind of contact occurs in a wide range from the test of general
skin contact to reinfusion situation during surgery. The most effective way to prevent
infection among patients is to use disposable probe but probe is complicated to be made
and expensive equipment so it should be reused. Thus, by adhering to the instructions for
use, risk of infection should be minimized among patients.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• Neurological treatment or test should not be conducted for patients with Creutzfeldt-
Jakob disease (a fatal brain disease caused by virus) and if probe was used, it cannot be
disinfected in any way.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Adequate cleaning and disinfection is required to prevent inspection. This is the

responsibility of the user managing and maintaining the immune process of equipment.
Always use the cleaner authorized by law.
Chapter 9 Probe 9-7

9.5.2 Risk of electrical shock
Since probe uses electrical energy, when contacting with a conductive material, it may
cause damage such as electrical shock to patients or users.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• Get regular electrical short tests from Samsung Medison Service team.
• You should not immerse probe in liquid enough to be waterlogged.
• Do not drop probe or apply mechanical shock to probe. Before • after use, check
dysfunction or damage of seal and lens, strain relief, housing.
• If twisting, pulling or bending probe cable excessively, it may be disconnected. Power
protection fuse protects probe and product from over current.
• If power monitoring protection circuit detects overcurrent, prevent the surface of probe
from overheating by immediately blocking current connected to probe and limit
ultrasound power output.
• The product limits the temperature that patients can contact to less than 43 degrees
Celsius and ultrasound output values comply with the limit standards of U.S. FDA.
Chapter 9 Probe 9-8

Service Manual
9.6 Use of protective cover (sheaths)

Sheath is used in tansvaginal test or rectal test that probe is inserted into the body. Also, by
using Sheath, let foreign substances coming from the body not be stained with probe in
surgery or biopsy test. Medison does not provide protective cover (Sheaths) so select and
use appropriate Sheath.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Keep Sheath sterile. Sheath is disposable so do not reuse it. If Sheath that was used in
probe was cut or contaminated, clean and disinfect probe.
• To apply neurosurgery, be sure to use sterile gel and non-thermal Sheath together in
sterile probe.
• If Sheath was used for patients with Creutzfeldt-Jacob''s disease during neurosurgery
treatment, probe cannot be disinfected in any way.
• Some Sheath conclude talc and natural rubber latex that may cause allergic reactions.
See FDA Medical Alert reported on March 29, 1991.
9.6.1 Sheath application

1. Take out Sheath from the packaging and then fill ultrasound gel. At this time, be sure to
wear disinfected gloves.
2. Put probe in Sheath and then, cover probe completely by pulling latex tip. If possible,
cover the cable of probe.
3. Be careful that air bubbles are not formed in ultrasound gel. If necessary, tie sheath to
probe and probe cable tightly.
4. After completing the test, discard Sheath.
Chapter 9 Probe 9-9

9.7 Cleaning and disinfection of probe
Inadequate pre-cleaners, disinfectants etc. may cause damage to probe.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• Wear face saver and gloves when cleaning or disinfecting probe.
9.7.1 Information of ultrasound gel, cleaners and disinfectants

Use appropriate cleaners and disinfectants, ultrasound gel by referring to the following
table. All probes were tested under IPX 7 condition.
Disinfectants
Sani-Cloth Active
Cleanisept Wipes
Trasneptic Spray
Super Sani-Cloth
Sani-Cloth Plus
Asepti-Wipes II
Sani-Cloth HB
Asepti-Wipes
Incidin Foam
Ster-Bac Blu
Setptiwipes
MetriWipes
Germicidal
CaviWipes
Sani-Cloth
T-Spray II
Cidex 2%
T-Spray
Names
Type S S W W W W W L S S W W W W W W L
Ammonium
Quaternary
(N-Alkyl)
IPA
NA
Active Ingredient
L4-7 ◆ ◆ ◎ ▣ ▲ ▣
L5-13IS ● ● ●
L7-16IS ● ● ●
C1-4 ◆ ◆ ◎ ▣ ▲ ▣
C2-6IC ● ● ●
C5-8 ◆ ◆ ◎ ▣ ▲ ▣
EC4-9IS ● ● ●
VR5-9 ◆ ◆ ◎ ▣ ▲ ▣
P2-4BA ● ● ● ● ●
V2-6 ◆ ◆ ◎ ▲ ▲ ▣ ▣
V4-8 ◆ ◆ ◎ ▲ ▲ ▣ ▣
V5-9 ◆ ◆ ◎ ▲ ▲ ▲ ▣ ▲ ■ ▲ ▲ ▲ ▣
CW2.0 ● ● ●
Chapter 9 Probe 9-10

L4-7
C5-8
C1-4
Type
Type
VR5-9
CW6.0
CW4.0
C2-6IC
Active
P2-4BA
L7-16IS
L5-13IS
Names
Names
EC4-9IS
Ingredient
Active Ingredient
S
T-Spray II
●
●
●
▲
▲
▲
▲
★
★
Cidex OPA 2,3)
S
T-Spray
●
●
●
●
●
Cidex Plus 2)
◇ ▣
◇ ▣
◇ ▣
◇ ▣
W
●
●
Metricide 2) Sani-Cloth HB
Quaternary
●
●
W
Omnicide (28) Sani-Cloth Plus

Ammonium
●
W
Omnicide 14NS Sani-Cloth Active

(N-Alkyl)
L
W
Omnicide - FG2 Setptiwipes

Glutaraldehyde
L
W
Nuclean Cleanisept Wipes

3)
●
●
L
▣
▣
▣
▣
Wavicide-01 Ster-Bac Blu
●
S
Sekusept Extra Trasneptic Spray
L
S
Disinfectants
Disinfectants
Salvanios pH 7 Incidin Foam
●
W
Salvanios pH10 Super Sani-Cloth

Sani-Cloth
●
W
Steranios 2% Germicidal
IPA
S
W
Surfaces Hautes Asepti-Wipes

Nonionic
L
W
Sekusept Plus Asepti-Wipes II

surfactant
W
CaviWipes
●
●
●
●
★
Milton
Sodium
Chapter 9 Probe
W
Hypochlorite MetriWipes
L Bleach 5.25%
L
NA Cidex 2%
Service Manual
9-11
Chapter 9 Probe
L4-7
V5-9
V4-8
V2-6
C5-8
C1-4
Type
VR5-9
CW6.0
CW4.0
CW2.0
C2-6IC
Active
V5-9
V4-8
V2-6
P2-4BA
L7-16IS
L5-13IS
Names
EC4-9IS
CW6.0
CW4.0
CW2.0
Ingredient
9-12
x
L
●
●
●
●
NA Virkon
●
▲
▲
▲
L
Sporox
Hydrogen Peroxide
x
x
x
●
●
●
Sporox Ⅱ
◇ ▣
▣
▣
◎
Gigasept
Succindialdehyde,
formaldehyde
x
x
x
L
◎
◎
◎
◎
◎
Gigasept AF 3)
●
●
Disinfectants
◎
◎
◎
◎
◎
★
◎
◎
Bersteinsaure Gigasept FF
Chlorhexidine gluconate
●
◎
◎
◎
◎
solution Hibitane
●
▣
▣
▣
▲
▲
▲
▲
▲
▲
▲
Peracetic Acid PeraSafe
Dodecylphenolethoxylat
●
●
●
●
●
e, Sodium Xylene Enzol

Sulfonate
●
NA Alkazyme
●
Cidezyme
Proteolytic Enzymes
L
●
●
●
●
●
◐
Klenzyme
Cleaner
◎
Isopropyl
x
x
L
●
●
alcohol(70%)
Alcohol
Isopropyl
L
alcohol(80%)
L4-7
V5-9
V4-8
V2-6
C5-8
C1-4
Type
VR5-9
CW6.0
CW4.0
CW2.0
C2-6IC
Active
P2-4BA
L7-16IS
L5-13IS
Names
EC4-9IS
Ingredient
x
L
●
●
●
●
NA Virkon
L
Sporox
Hydrogen Peroxide
x
x
x
L
●
●
Sporox Ⅱ
L
◎
Gigasept
Succindialdehyde,
formaldehyde
x
x
x
L
◎
◎
◎
◎
◎
Gigasept AF 3)
L
●
●
Disinfectants
◎
◎
◎
◎
◎
★
◎
◎
Bersteinsaure Gigasept FF
Chlorhexidine gluconate
L
●
◎
◎
◎
◎
solution Hibitane
P
▲
▲
▲
▲
▲
▲
▲
Peracetic Acid PeraSafe
Dodecylphenolethoxylat
●
●
●
e, Sodium Xylene Enzol
Sulfonate
●
NA Alkazyme
L
Cidezyme
Proteolytic Enzymes
L
●
●
●
●
●
◐
Klenzyme
Cleaner
Isopropyl
x
x
x
L
●
alcohol(70%)
Chapter 9 Probe
Alcohol
Isopropyl
L
alcohol(80%)
Service Manual
9-13
Chapter 9 Probe
L4-7
V5-9
V4-8
V2-6
C5-8
C1-4
Type
VR5-9
CW6.0
CW4.0
CW2.0
C2-6IC
Active
P2-4BA
L7-16IS
L5-13IS
Names
EC4-9IS
9-14
Ingredient
Alcohol L
L Ethanol 75%
●
●
●
●
Propylene Glycol Metrizyme
Cleaner
PCMX McKesson
L
(Chloroxylenol)
Ammonium
G
Chlorides Natural Image

G
●
●
●
●
●
●
●
●
●
●
●
●
●
●
●
Aquasonics 100 3)
GE Ultrasound
G
Contact Gel
●
●
●
G
Clear Image
Gel
Kendall
NA
G
Scan
●
●
●
●
●
●
G
Wavelength
G
Sonogel
●
●
●
●
●
●
Service Manual
※ Meanings of symbols
The meanings of the symbols shown in the table are as follows:
(1) Compatible but no EPA Registration
(2) FDA 510(k) qualified
(3) Has CE mark
(4) Discontinued
(5) Under Development
S Spray
W Wipe
L Liquid
P Powder
G Gel
x Not compatible(DO NOT USE)
● Compatible
Staining may occur on housing parts; however, the acoustic performance
★
and image quality are not affected.
■ Must not be used longer than 5 minutes.
◐ Must not be used longer than 10 minutes.
▲ Must not be used longer than 15 minutes.
◆ Must not be used longer than 20 minutes.
◇ Must not be used longer than 25 minutes.
◎ Must not be used longer than 30 minutes.
▣ Must not be used longer than 50minutes.
Blank Untested (DO NOT USE)
Manufacturer information of cleaners and disinfectants, ultrasound gel is as follows.
Product Manufacturer or Distributor Telephone number
Aquasonics Parker Co. +1-800-631-8888(USA)

+1-800-445-6741(USA)
Cidex CIVCO Co.
+1-319-656-4447(Worldwide)
+1-800-445-6741(USA)
Enzol CIVCO Co.
+1-319-656-4447(Worldwide)
GIgasept AF S&M(Schulke&Mayr) Co. +44-114-254-3500(UK)
Gigasept FF S&M(Schulke&Mayr) Co. +44-114-254-3500(UK)
Isoproppyl alcohol (70%) Local drugstore None
Klenzyme Steris Co. +1-800-548-4873(USA)
+1-800-445-6741(USA)
Metricide CIVCO Co.
+1-319-656-4447(Worldwide)
Metrizyme Metrex Research Corp. +1-800-841-1428(USA)

Product Manufacturer or Distributor Telephone number
Procter & Gamble Australia Pty.

Milton +61-1800-028-280(Australia)
Ltd.
+1-800-526-3867(USA)
Nuclean National Diagnostics Co.
+44(0)-148-264-6020(UK)
Omnicide Cottrell Ltd. +1-800-843-3343 (USA)
Sani-cloth PDI/Nice-Pak Products Co. +1-914-365-1602(USA)
Sekusept Extra Henkel Hygiene GmbH. +49-0211-797-0(Germany)
Sporox II Sultan Chemist Inc. +1-800-637-8582(USA)
+1-800-445-6741(USA)
T-Spray CIVCO Co.
+1-319-656-4447(Worldwide)
Virkon Antec International LTD. +1-403-286-1771(USA)
Wavicide Wave Energy System Inc. +1-800-252-1125(USA)
9.7.2 Cleaning
Cleaning of probe is the important step done prior to disinfection and be sure to clean
probe after use it.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Do not use surgical brush to clean probe. Be careful because even soft brush may
cause damage to probe.
• When cleaning and disinfecting, dry with set area faced down so that liquid ingredient
cannot come into probe.
1. Separate probe from the system.
2. Separate Needle guide and adapter for biopsy (adapter can be reused through
disinfection)
3. Separate Sheath. (Sheath is disposable.)
4. Wipe foreign substances left in cable and probe with soft cloth dampened with soap
or cleaning fluid.
5. To clean remaining foreign substances, dip even the waterproof part in water and
rinse it.
6. Wipe water with dry cloth.
7. If soap remains, wipe with cloth moistened with water and wipe again with dry cloth.

Service Manual
9.7.3 Disinfection
To reduce Pathogens to 10-6, disinfect probe by using disinfectant recommended by
Medison.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• If using a mixed solution, note the expiry date of the solution.

• The level of disinfectant differs depending on body tissues where probe is contacted so
note intensity and disinfection time of disinfectant.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• If using not recommended disinfectant or not disinfecting with the presented disinfecting
method, probe may be damaged or discolored. The product cannot be guaranteed.
• Do not immerse probe that cannot be disinfected in disinfectant for more than one hour.
Use only liquid solution. Disinfection using Autoclave, EtO gas etc. is prohibited.
1) For storage, use, disposal etc. of disinfectant, see the user’s manual of
disinfectant.
2) Mix disinfectant appropriate for probe to be used depending on the intensity of the
solution set forth in the manual of disinfectant.
3) Immerse the probe in the disinfecting solution in the way of the following figure.
4) Rinse probe after dipping work according to the instructions written in disinfectant
solution.
5) Dry probe in the air or wipe it with dry cloth.
[Figure 9-1] How to disinfect probe

Chapter 10
Maintenance and Management
Service Manual
Chapter 10 Maintenance and Management
10.1 Overview
Chapter 10 describes the contents to improve the life of ACCUVIX A30. It provides how to
store the product and how to back up information etc.
Be sure to read it for proper maintenance and management.
Contents
10.1 Overview ................................................................................................................ 10-1

10.2 Product management ........................................................................................... 10-2
10.2.1 Use environment..................................................................................... 10-2
10.2.2 Cleaning and disinfection....................................................................... 10-2
10.2.3 Air Filter management ............................................................................ 10-4
10.2.4 Accuracy test ........................................................................................... 10-5
10.3 Information management ..................................................................................... 10-5
10.3.1 User Setting Back-up ............................................................................. 10-5
10.3.2 Patient information Restore ................................................................... 10-5
10.3.3 Software ................................................................................................... 10-5
Chapter 10 Maintenance and Management 10-1

10.2 Product management
10.2.1 Use environment

Consider the followings when installing the product.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙

broadcasting station, abnormal screen due to noise may occur. Also, using the same
power with other electric appliances can cause noise.
■ Avoid watery places

■ Keep the product out of the direct rays of the sun.
■ Avoid places showing drastic temperature fluctuations.
■ For normal operation, 10 OC ~ 35 OC of temperature and 30% ~ 75% of humidity
should be maintained.
■ Avoid installing the product in places where heating appliances are close.
■ Avoid dusty or poorly ventilated places.
■ Avoid places with frequent vibrations.
■ Avoid places where there are chemicals or gases
10.2.2 Cleaning and disinfection

Inadequate detergent or disinfectant etc. may damage the product.
Read the following.
˙A
W ˙R
˙N˙ ˙IN
˙G˙
• Before cleaning or disinfecting, be sure to turn off power of the product or unplug the
power cord. It may cause electrical shock or fire.
• When cleaning or disinfecting the product, always wear face saver and gloves.
10.2.2.1 Cleaning

Service Manual
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Do not spray cleaner directly on the outside of the product.

• Components may be discolored or cracked.
• Do not use chemicals such as wax, benzene, alcohol, thinner, mosquitocide, air
freshener, lubricant, cleaner etc.
 Console
Wipe the external surface of the product with soft cloth dampened with detergent or mild
soap.
 Monitor cleaning
Wipe the LCD surface with soft and dry cloth.
If LCD panel is smeared with foreign substances, wipe it gently more than 2-3 times in the
same direction.
˙O
N ˙ T˙ E˙
• For cleaning and disinfection of probe, see ‘Chapter 9 probe’ of this manual.
10.2.2.2 Disinfection
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Be sure to disinfect the surface with disinfectant presented by Samsung Medision.
We recommend you to disinfect the product with disinfectant approved by U.S FDA 510(k).
The followings are the products approved by U.S FDA 510(k) and disinfectants suitable for
this product.
Manufacturin FDA
Disinfectant Form solution
g country 510(k)
Cidex USA Liquid GLUTARALDEHYDE K934434
Cidex Plus USA Liquid GLUTARALDEHYDE K923744
1. Turn off the power of the product and unplug the power cord.

2. Mix according to the percentage indicated in the manual of disinfectant.
3. Wipe the surface of the product by referring to the instructions written in the manual of
disinfectant.
4. Wipe with dry cloth indoors according to the instructions written in the manual of
disinfectant.
10.2.3 Air Filter management

Air filter minimizes dust from entering the product. Dust-filled filters cause product
overheating or noise. Also, it may be the cause of reducing reliability and performance of
the system. Keep your system optimized by cleaning the filter every three months.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Before removing or installing a filter, be sure to check the moving locking device. You
may get injured due to unexpected movement of the product.
[Figure 10.1 Removing air filter]
1. Remove the filter from the product by pulling it under the console front
2. Remove dust by beating the filter and then clean it by using with mild detergent.
3. Wipe moisture with a dry towel and then dry the filter in the shady and well-ventilated
area.

Service Manual
4. Complete installation by pushing the filter fully.
˙O
N ˙ T˙ E˙
• If installing a moistful filter, it may cause malfunction of the product.

• Be sure to install a fully dried filter
10.2.4 Accuracy test
˙O
N ˙ T˙ E˙
• A user should conduct safety inspection every two years according to EN60601-1, safety
standards requirement. Only professional staff can perform safety inspection.
Measured values obtained by this product are affected by the management status of the
product. Manage the product in the optimal state for reliable measured values. Perform
the measurement accuracy test annually to maintain optimal product state.
Equations related to measurement accuracy and related tables are included in ‘Chapter 5.
Measurement’ of this manual.

10.3 Information management
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• Back up periodically because stored information may be lost due to external shocks or its
own error.
10.3.1 User Setting Back-up

Record User Setting related information in case data is lost. A user cannot directly perform
the work backing up User Setting of the product and a service department employee
should conduct Back-up at the request of customers.
10.3.2 Patient information Back up

Patients’ basic information and scanned images can be backed up through SONOVIEW
program. They can be directly saved by a user and basically saved in the system. If
System needs to be reinstalled due to the problems of the product, a service department
employee restores saved patients’ basic information and images. For more information,
see ‘Chapter 6 image management’.
10.3.3 Software
Software may be changed to improve the functions of the product. A user cannot
independently change software and should change it according to cooperation of Medison
Co., Ltd employees.
˙A
C ˙U
˙ T˙ ˙IO
˙N˙
• The small changes of software are subject to change without notice of the manufacturer.
TM
When there is a problem with operating system (Windows ) or it needs to be upgraded,
you should follow the manufacturer standards of the operating system.

Chapter 11
Service parts list
Service Manual
Chapter 11 Service parts list

11.1 Overview
Chapter 11 provides information on service parts of ACCUVIX A30. Before ordering
service parts, be sure to check compatibility of software version and service parts. See
ACCUVIX A30 Part Catalogue provided by Samsung Medison Co. Ltd, Global Service
Group for the checking method.
Contents
11.1 Overview ................................................................................................................ 11-1

11.2 Body Cover ............................................................................................................ 11-2
11.3 Ultrasound System Part ...................................................................................... 11-4
11.4 LCD & ARM ........................................................................................................... 11-5
11.5 PC Part ................................................................................................................... 11-6
11.6 Power Part ............................................................................................................. 11-8
11.7 User Interface Part ................................................................................................ 11-9
11.8 ETC Part............................................................................................................... 11-10
11.9 Options ................................................................................................................. 11-11
[Figure 11-1] ACCUVIX A30 Views
Chapter 11 Service parts list 11-1

11.2 Body Cover
4
8
1 7
9
18
14
17
13
19 11
16 15
10
[Figure 11-2] Body Cover

Service Manual
PART NAME PART NUMBER DESCRIPTION
1 COVER FRONT LOWER MI97-01465B COVER FRONT LOWER ACCUVIX A30
2 HANDLE UPPER ACCUVIX XG MI64-01659A HANDLE UPPER ACCUVIX XG
3 COVER PALM REST MI63-01372A COVER PALM REST ACCUVIX A30
4 CP ASSY EXP MI95-01203A CP ASSY EXP ACCUVIX A30
5 LED 21.5Inch Monitor ASSY MI96-01002E LED 21.5 MNT AY ACCUVIX A30
6 COVER REAR BACK LCD MI63-01333A COVER REAR BACK LCD EKO7
7 COVER HANDLE AY MI97-01464B COVER HANDLE AY ACCUVIX A30
8 COVER TOP SIDE L MI63-01356A COVER TOP SIDE L ACCUVIX A30
9 COVER SIDE L MI63-01360A COVER SIDE L ACCUVIX A30
10 COVER REAR MI97-01466B COVER REAR AY ACCUVIX A30
11 CLAMP GROUNDING 6502-001247 CLAMP GROUNDING CABLE KTCC 5
12 SHIELD REAR MI97-01253B SHIELD REAR ACCUVIX A30
13 BRACKET DDM AY MI97-02057A BRACKET DDM AY ACCUVIX A30
14 COVER MID MI97-01499B COVER MID AY ACCUVIX A30
15 FILTER AY MI97-01318A FILTER AY ACCUVIX A30
16 COVER SIDE R MI63-01361A COVER SIDE R ACCUVIX A30
17 COVER TOP SIDE R MI63-01357A COVER TOP SIDE R ACCUVIX A30
18 COVER CP BOTTOM MI97-01460C COVER CP BOTTOM AY ACCUVIX A30
19 COVER PSA AY MI97-01462A COVER PSA AY ACCUVIXA30
[Table 11-1] ACCUVIX A30 Cover

11.3 Ultrasound System PCB Part
1 2
3 4 5
6
[그림 11-3] Ultrasound System Part
No PART NAME PART NUMBER DESCRIPTION
1 PSA Board MI92-01640C PSA Board ACCUVIX A30
2 Analog Control BD MI92-01762A Analog Control BD ACCUVIX A30
3 CW Board MI92-01640C CW Board ACCUVIX A30
4 BF Board MI92-01766A BF Board ACCUVIX A30

ASSY BOARD-PCC;A30,PCC,0A,PC-
5 PCC Module MI92-02290A
BACKEND
6 Rear Board _ Right MI92-02299A ASSY BOARD-RR;A30 V3.0,,REAR
6 Rear Board _ Left MI92-02314A ASSY BOARD-RL;A30 V3.0,RL,1A,REAR

ASSY SMD-PCC;A30,PCC,0A,PC-
7 PCC Board MI92-02292A
BACKEND
8 PCC VGA 5902-005111 CARD VGA;N650GTX-1G
[Table 11-2] Ultrasound System Part

Service Manual
11.4 LCD & ARM Part
4 5
[Figure 11-4] LCD & ARM Part
1 LED 21.5Inch Monitor ASSY MI96-01002E LED 21.5 MNT AY ACCUVIX A30
2 COVER REAR BACK LCD MI63-01333A COVER REAR BACK LCD ACCUVIX A30
3 Arm ASSY MI97-01029A UNIV ARM AY ACCUVIX A30
4 Base Lower Back Unit Arm Cover MI63-01244A Base Lower Back Unit Arm Cover
5 Base Lower Front Unit Arm Cover MI63-01245A Base Lower Front Unit Arm Cover
[Table 11-3] LCD & ARM Part

11.5 PC Part
1 2
[그림 11-5] PC Part
1 PC Module MI96-01303B ASSY PC-MODULE;A30 V3.0
2 PCC VGA 5902-005111 CARD VGA;N650GTX-1G
3 Seagate 500G HDD 5903-004129 HDD;ST3500312CS
[Table 11-4] PC Part

Service Manual
11.6 Power Part
[Figure 11-6] Power Part
1 DDM Power MI96-01300B Power ASSY DC to DC Module ACCUVIX A30
2 ADM Power MI97-01236C Power ASSY AC to DC Module ACCUVIX A30
[Table 11-5] Power Part

11.7 User Interface Part
1 2 3
5 6
4
[Figure 11-7] User Interface Part
1 Control Panel Board MI92-02305A Control Panel Board ACCUVIX A30

Alpha-numeric
2 MI95-01240B ALPHA KBD ASSY ACCUVIX A30
Keyboard
3 Touch Panel MI96-01184D TOUCH PANEL AY ACCUVIX A30
4 Track Ball Unit 58mm MI59-01060B Track Ball Unit 58mm
5 Speaker ASSY 3001-002724 Speaker Left ASSY
6 ECG USB ASSY USO-UA3EA00/WR ECG ASSY ACCUVIX A30
7 ODD 5903-005017 SUPER MULTI 22X SATA ODD BLACK
[Table 11-6] User Interface Part

Service Manual
11.8 ETC Part
1 2
3 4
[Figure 11-8] ETC Part
1 Rear Fan ASSY MI96-01075A Rear Fan ASSY ACCUVIX A30
2 System Fan ASSY MI97-01589B System Fan ASSY ACCUVIX A30
3 RUBBER CENTER MI64-01608A RUBBER CENTER ACCUVIX A30
4 RUBBER LEFT MI64-01609A RUBBER LEFT ACCUVIX A30
[Table 11-7] ETC Part

11.9 Options
1 4D USO-UA3S400/WR 4D
2 3DMXI USO-UA33X00/WR 3D XI
3 3DXI USO-UA33D00/WR 3DXI, XI STIC
4 3DXIST USO-UA3ST00/WR 3DXIST
5 AUTO IMT USO-UA3AT00/WR AUTOIMT
6 ADVR USO-U0NAUS0/WR ADVR
7 CARDIAC USO-UA3CA00/WR CARDIAC MEASURMENT
8 CW USO-UA3CWP0/WR CW PACKAGE OPTION
9 DICOM USO-UA3DI00/WR DICOM
10 ECG USO-UA3EI00/WR ECG MODULE OPTION
11 ELASTOSCAN USO-UA3ES00/WR ELASTOSCAN
12 PANORAMIC USO-UA3PN00/WR PANORAMIC
13 SCI USO-UA3SI00/WR SCI
14 VOLUMENT USO-UA3VI00/WR VOLUME NT
[Table 11-8] Options

A30 SERVICE MANUAL
Publisher SAMSUINGMEDISON Co., Ltd

Address SAMSUNGMEDISON Bldg., 42 Teheran-ro 108-gil, Gangnamm-gu,
Seoul 135-280 Korea
Homepage http://www.samsungmedison.com

Accuvix A30 SVM V3.0 Rev2 Eng

Uploaded by

Document Information

Original Title

Copyright

Available Formats

Share this document

Share or Embed Document

Sharing Options

Did you find this document useful?

Is this content inappropriate?

Copyright:

Available Formats

Accuvix A30 SVM V3.0 Rev2 Eng

Uploaded by

Copyright:

Available Formats

A30 Service Manual

Recovery S/W Compatibility

Copyright©2012 by Samsung Medison

▶ Type of protection against electrical shock: Class I

Electromechanical safety standards met:

This is CSA symbol for Canada and United States of America

This is manufacturer’s declaration of product compliance

This is manufacturer’s declaration of product compliance

This is GMP symbol for Good Manufacturing Practice of

Certificate of Excellent Service Quality is to certify that the

1. Refer to the service manual when repairing the product.

 This is warning to prevent damage of property or serious accidents.

 This is caution to prevent minor accidents and property damage.

 This is information for users such as installation requiring attention, operation or

Chapter 1 About product

3.17 DICOM Setup (option) ...................................................................................................3-36

Chapter 4 Product inspection

Chapter 5 Product Structure

Chapter 6 Basic maintenance

Chapter 7 Diagnosis of failure

7.4 Error message .................................................................................................................. 7-5

Chapter 10 Maintenance and management

10.2.3 Air Filter management ....................................................................................10-4

Chapter 11 Service Parts List

1.1 Overview .................................................................................................................. 1-1

Chapter 1 Safety 1-1

1.2.1 Safety symbols

Warning on the danger of electrical shock

Classification according to the degree of protection on

Classification according to the degree of protection on

Power switch (Supplying/shutting off power to products)

OFF(Shutting off power supply to part of the product)

WARNING: This is the warning to prevent serious

CAUTION: This is the attention to prevent minor accidents

See the service manual

ON (Supplying power to part of the product)

Chapter 1 Safety 1-2

High-tension part greater than alternating 1000 V or direct

Protective earth terminal

Data output port

Data input port

Data input and output port

Left and right audio / Video input port

Left and right audio / Video output port

Print remote output

Foot switch connector

Flood proof type device

Drip proof type device

Chapter 1 Safety 1-3

ESD related warning sign

Do not sit on control panel.

Follow the service manual

Chapter 1 Safety 1-4

[Label 2. Caution attached to the bottom of OUTLET]

[Label 3. ‘TIP-OVER’ related attention]

Chapter 1 Safety 1-5

[Label 5. Probe ID Label]

Chapter 1 Safety 1-6

1.3 Electrical Safety

1.3.1 Prevention of electrical shock

[Figure 2-6] Connection of equipotential terminal

Connected peripheral devices should comply with IEC standards (Data

Chapter 1 Safety 1-7