EDAN Acclarix AX4 User manual

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文件名称(Document Name)：Acclarix AX4 使用说明书基础册-英文
文件编号(Number)：01.54.457698
版本(Version)：1.6
产品型号(Product Model)：Acclarix AX4
项目编码(Project Code)：2908G004
签批信息(Signature):
作者(Originator) : 谢 菊艳 (xiejuyan) 2019-12-25 09:51:01
审核人(Reviewers) : 李 娟 (lijuan) 2019-12-25 17:51:54
审核人(Reviewers) : 郭 伟娟 (guoweijuan) 2019-12-26 16:30:26
审核人(Reviewers) : 刘 恒 (liuheng) 2019-12-25 14:25:34
审核人(Reviewers) : 熊 文 (xiongwen) 2019-12-26 14:55:23
审核人(Reviewers) : 冀 伟 (jiwei) 2019-12-25 13:46:20
审核人(Reviewers) : 屈 培 (qupei) 2019-12-25 17:25:10
审核人(Reviewers) : 郭 亮 (guoliang) 2019-12-25 13:11:30
审核人(Reviewers) : 张 仁富 (zhangrenfu) 2019-12-26 11:13:53
审核人(Reviewers) : 鲁 应君 (luyingjun) 2019-12-26 10:34:54
批准人(Approvers) : 鲁 应君 (luyingjun) 2019-12-27 14:55:35
版权©深圳市理邦精密仪器股份有限公司 (Copyright©Edan Instrument,Inc.)

1

I
Preface
This User Manual Basic Volume together with the User Manual Advanced Volume
(P/N:01.54.457699) contain necessary and sufficient information to use the Acclarix AX4
Ultrasound Imaging Systems safely for the intended purposes and approved clinical applications.
This User Manual applies to the Acclarix AX4 1.2X releases.
Please read and make sure you understand all of the instructions in this manual prior to using the
system.
Not all measurements and features are available for all system models and configurations. This
manual is based on the complete set of transducers and features available. Therefore, some of the
contents may not apply to your product. If you have any questions, please contact your local
EDAN representative.
Disregarding instructions, particularly warnings and cautions, is considered abnormal use.
Caution: Federal law restricts this device to use by, or on the orders of a physician.
Contact Information:
For sales or service information, please contact your local distributor or the EDAN Service
Department at: [email protected]
P/N:01.54.457698
MPN: 01.54.457698016
Release Date: Dec. 2019
© Copyright EDAN INSTRUMENTS, INC. 2017-2019

II
RegulatoryApproval Remarks
Auto OB measurement IS NOT available in the USA and its territories.
The following features are not available in Canada at the time of release of this user manual.
Consult your local representatives for the availability of these features.
Auto IMT measurement
Anatomic M mode
TDI mode
Color One-key optimization
Auto OB measurement
MC9-3TQ transducer

III
Contents
1 Introduction..............................................................................................................................1
1.1 Intended Use/ Indications for Use..........................................................................................1
1.2 Contra-indications..................................................................................................................1
1.3 Device Description.................................................................................................................1
1.4 Labeling Symbols ..................................................................................................................2
2 Safety.........................................................................................................................................5
2.1 Warnings.................................................................................................................................5
2.2 Cautions .................................................................................................................................7
3 Getting Started....................................................................................................................... 11
3.1 System Configuration ..........................................................................................................11
3.2 System Overview.................................................................................................................13
3.3 Battery Use...........................................................................................................................15
3.4 Connecting and Disconnecting a Transducer.......................................................................16
3.5 Powering on/ off...................................................................................................................18
3.6 Screen Layout.......................................................................................................................20
3.7 Control Panel........................................................................................................................23
3.8 Touch Screen........................................................................................................................25
3.9 Trackpad...............................................................................................................................27
4 Exam Operation.....................................................................................................................28
4.1 How to Start an Exam..........................................................................................................28
4.2 How to End an Exam ...........................................................................................................28
4.3 How to Restart an Exam ......................................................................................................29
4.4 The Patient Information Page...............................................................................................29
4.5 Modality Worklist ................................................................................................................31
5 Imaging...................................................................................................................................33
5.1 B-mode.................................................................................................................................33
5.1.1. B-mode Touch Screen Controls.................................................................................33
5.1.2. Dual Imaging .............................................................................................................36
5.1.3. Quad Imaging ............................................................................................................36
5.1.4. Panorama ...................................................................................................................37
5.1.5. Zoom..........................................................................................................................37
5.2 PW-mode..............................................................................................................................38
5.2.1. PW Touch Screen Controls........................................................................................38
5.2.2. HPRF .........................................................................................................................40
5.2.3. Update........................................................................................................................40
5.3 CW-mode .............................................................................................................................40
5.3.1. CW Touch Screen Controls........................................................................................40
5.4 Color mode...........................................................................................................................42
5.4.1. Color Touch Screen Controls.....................................................................................42
5.4.2. Color Mode Variants..................................................................................................44
5.5 M-mode................................................................................................................................45
5.5.1. M-mode Touch Screen Controls................................................................................45
5.6 Anatomic M Mode ...............................................................................................................46
5.6.1. Anatomic M Touch Screen Controls..........................................................................46
5.6.2. Anatomic M Mode Operations..................................................................................46
5.7 TDI Mode.............................................................................................................................47

IV
5.7.1. TDI Mode Operations................................................................................................47
5.7.2. TDI Touch Screen Controls .......................................................................................47
5.8 3D/4D Mode ........................................................................................................................47
5.8.1. Pre-3D/Pre-4D ...........................................................................................................48
5.8.2. 3D Volume Sweeping ................................................................................................49
5.8.3. 3D Image Review ......................................................................................................49
5.8.4. 4D Volume Acquisition..............................................................................................54
5.8.5. 4D Live Volume.........................................................................................................55
5.8.6. 4D Cine......................................................................................................................55
5.8.7. 3D/4D Dataset............................................................................................................56
6 Transducers............................................................................................................................57
6.1 Transducer Model ................................................................................................................57
6.2 Name and Function of Each Part of the Transducer ............................................................58
6.3 Transducer Cleaning and Disinfecting.................................................................................58
6.3.1. Cleaning.....................................................................................................................58
6.3.2. Disinfection................................................................................................................59
6.3.3. Sterilization................................................................................................................62
6.3.4. Storage .......................................................................................................................62
6.3.5. Using Transducers......................................................................................................63
7 Features...................................................................................................................................65
7.1 Comments ............................................................................................................................65
7.2 Body Mark ...........................................................................................................................67
7.3 Measurements ......................................................................................................................68
7.3.1. Generic Measurements ..............................................................................................70
7.3.2. Application Measurements and Calculations ............................................................78
7.4 Patient Information Management.........................................................................................84
7.4.1. Storing Images...........................................................................................................84
7.4.2. Reviewing Images......................................................................................................84
7.4.3. Patient Database.........................................................................................................87
7.4.4. Archiving Studies ......................................................................................................88
7.4.5. Structured Report.......................................................................................................89
7.5 Needle Biopsy Guide ...........................................................................................................90
7.5.1. Installing Needle Guide Bracket................................................................................90
7.5.2. Activating Needle Guide Function ............................................................................94
7.5.3. To Adjust the Needle Guide Line ..............................................................................95
7.6 Needle Visualization ............................................................................................................95
8 Presets.....................................................................................................................................97
8.1 Preset Organization..............................................................................................................97
8.2 Selecting a Preset .................................................................................................................98
8.3 Storing a Preset ....................................................................................................................98
8.3.1. Presets........................................................................................................................99
8.3.2. Comments Presets....................................................................................................102
8.3.3. Bodymarker Presets.................................................................................................103
8.3.4. Measure Presets .......................................................................................................105
9 Utilities..................................................................................................................................109
9.1 Set-up .................................................................................................................................109
9.1.1. General Set-up .........................................................................................................110
9.1.2. Patient Set-up........................................................................................................... 111

V
9.1.3. Store/Print Set-up.....................................................................................................112
9.1.4. Miscellaneous Set-up............................................................................................... 114
9.1.5. User Set-up ..............................................................................................................115
9.2 Connectivity.......................................................................................................................116
9.2.1. TCP/IP .....................................................................................................................116
9.2.2. DICOM....................................................................................................................118
9.2.3. Network Store..........................................................................................................120
9.3 Maintenance.......................................................................................................................122
9.3.1. License.....................................................................................................................122
9.3.2. Version .....................................................................................................................122
9.3.3. Demo........................................................................................................................123
9.3.4. Export/Import...........................................................................................................124
9.4 Screen Adjust .....................................................................................................................125
10 In Between Exams................................................................................................................127
10.1 Unpacking........................................................................................................................127
10.2 Transport ..........................................................................................................................127
10.3 Storage .............................................................................................................................127
11 Order List.............................................................................................................................128
12 Troubleshooting and Maintenance.....................................................................................130
12.1 Daily Checklist.................................................................................................................130
12.2 Troubleshooting ...............................................................................................................130
12.3 Maintenance.....................................................................................................................131
12.4 Cleaning the System.........................................................................................................131
12.4.1. Cleaning the System Surface...................................................................................132
12.4.2. Needle Guide Bracket Cleaning and Sterilization...................................................132
13 Specifications........................................................................................................................134
13.1 Electrical Safety Classifications.......................................................................................134
13.2 Power Supply...................................................................................................................134
13.3 Machine Specifications....................................................................................................134
13.4 Display Specifications......................................................................................................135
13.5 General Technical Specifications.....................................................................................135
13.6 Operating, Storage and Transportation Environment.......................................................137
13.6.1.Operating Environment.............................................................................................137
13.6.2.Storage and Transportation Environment..................................................................137
14 EMC Information................................................................................................................138

AcclarixAX4 Diagnostic Ultrasound System User Manual Introduction
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1 Introduction
1.1 Intended Use/ Indications for Use
The Ultrasound system is intended for use by a qualified physician or allied health professional
for ultrasound evaluations. Specific clinical applications include:
Abdominal
Gynecology (including endovaginal)
Obstetric
Cardiac
Small Parts (Breast, Testes, Thyroid, etc.)
Urology
Musculoskeletal
Peripheral Vascular
Intra-operative
Pediatric
Neonatal (including abdominal and cephalic)
Adult Cephalic
1.2 Contra-indications
The ultrasound system is not intended for ophthalmic use or any use causing the acoustic beam to
pass the eye.
1.3 Device Description
The Acclarix Ultrasound Imaging System consists of a main system and associated ultrasound
transducers.
The system circuitry generates an electronic voltage pulse, which is transmitted to the
transducer. In the transducer, a piezoelectric array converts the electronic pulse into an
ultrasonic pressure wave. When coupled to the body, the pressure wave transmits through body
tissues. The waves are then reflected within the body and detected by the transducer, which
then converts the waves back to an electrical signal. The Acclarix system then analyzes the
returned signals and generates an ultrasound image or spectral Doppler display.
The Acclarix Ultrasound Imaging System provides the operator the ability to measure
anatomical structures, and offers analysis packages that provide information used by competent
health care professionals to make a diagnosis.
The system’s user interface provides both hard keys for functions frequently used throughout
an exam and touch screen controls for mode-specific functions.

AcclarixAX4 Diagnostic Ultrasound System User Manual Introduction
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1.4 Labeling Symbols
The following labels are used on the system:
No.
Symbol
Definition
1
Serial Number
2
P/N
Part Number
3
Date of Manufacture
4
Manufacturer
5
Operating instructions
6
Warning
(Background: Yellow; Symbol & outline: Black )
7
Refer to User Manual
(Background: Blue; Symbol: White)
8
Caution
9
Biological Risks
10
CE Marking
11
Authorized Representative in the European Community
12
Disposal method. Indicates that the equipment should be
sent to special agencies according to local regulations for
separate collection after its useful life.
13
General Symbol for Recovery / Recyclable
14
Caution: Federal (U.S.) law restricts this device to sale by or
on the order of a physician.
15
IPX7
No harm for short time immersion

AcclarixAX4 Diagnostic Ultrasound System User Manual Introduction
- 3 -
16
Type BF Applied Part
17
Transducer connector
18
Pencil Transducer connector (reserved)
19
ECG signal input connector (reserved)
20
Transducer lock
21
Transducer unlock
22
Network port
23
Trademark
24
Direct current
25
Video Output port
26
USB 2.0 port
27
USB 3.0 port
28
Display port
29
Microphone input
30
Headphones
31
Non-ionizing electromagnetic radiation
32
FCC ID:SMQAX8EDAN
Federal Communications Commission:
FCC ID:SMQAX8EDAN

AcclarixAX4 Diagnostic Ultrasound System User Manual Introduction
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33
Non-sterile. Indicates a medical that has not been subjected
to a sterilization process.
34
Conforms to AAMI Std. ES 60601-1, IEC Std. 60601-2-37,
IEC Std. 60601-1-6
Certified to CSA Std. No. 60601-1, No 60601-2-37, No.
60601-1-6
The following labels are used on the packaging:
No.
Symbol
Definition
1
This way up
2
Fragile, handle with care
3
Keep dry
4
General Symbol for Recovery / Recyclable
5
Stacking limit by number
6
Do not step on!
7
Handle with care
NOTE:
The user manual is printed in black and white.

Acclarix AX4 Diagnostic Ultrasound System User Manual Safety
- 5 -
2 Safety
Throughout this document the following terms are used:
Warning: Advises against certain actions or situations that could result in personal injury
or death.
Caution: Advises against actions or situations that could damage equipment, produce
inaccurate data, or invalidate a procedure.
Note: Provides useful information regarding a function or a procedure.
Please read all warnings and cautions prior to using the system. For your convenience, all
warnings and cautions are provided in this section, but may be duplicated elsewhere in this
document in the context of the instructions for use.
2.1 Warnings
Only use an Edan supplied power adapter and power cord.
Only use an Edan supplied battery. Read and understand the battery installation
instructions prior to changing the battery.
Only use Edan supplied transducer. Use of other transducers may result in electric
shock or system malfunction.
Only use a hospital grade, grounded, power outlet and plug. Do not use with an
ungrounded outlet.
The system is ordinary equipment (sealed equipment without liquid proof).
However, the system console panel including touch screen, track pad and hard
keys are IPX1 certified. The transducers (not including transducer connector) is
IPX7 certified. The footswitch is IP68 certified. Do not immerse or expose any of
the parts to extended moisture. Splash resistance does not extend to transducer
connectors. Please keep connectors dry.
Do not use in a wet environment or when the relative humidity exceeds 95%.
Do not reverse the positive and negative poles when installing the battery.
Do not use the battery near heat sources or when the ambient temperature is over
40oC. Do not heat or dispose of in fire.
Do not destroy the battery; do not pierce or cause a strong impact to the battery.
Do not touch the connector pins on the transducer port.
Parts and accessories used must meet the requirements of the applicable
IEC/EN60601 series safety standards, and/or the system configuration must meet
the requirements of the IEC/EN60601-1.
Use protective barriers (gloves and transducer sheaths) whenever possible.
Follow sterile procedures when appropriate. Thoroughly clean Transducers and
reusable accessories after each patient examination and disinfect or sterilize as
needed. Refer to transducer use and care instructions. Follow all infection control
policies established by your office, department or institution as they apply to

Acclarix AX4 Diagnostic Ultrasound System User Manual Safety
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personnel and equipment.
Not intended for Ophthalmic use.
If a sterile transducer cover becomes compromised during an intra-operative
application involving a patient with transmissible spongiform encephalopathy, such
as Creutzfeldt-Jakob disease, follow the guidelines of the U.S. Disease Control
Center and this document from the World Health Organization:
WHO/CDS/APH/2000/3, WHO Infection Control Guidelines for Transmissible
Spongiform Encephalopathies. The transducers for your system cannot be
decontaminated using a heat process.
Contact with natural rubber latex may lead to a severe anaphylactic reaction in
persons sensitive to the natural latex protein, Sensitive users and patients must
avoid contact with these items. EDAN strongly recommends that health-care
professionals identify their latex-sensitive patients, and refer to the March 29, 1991
Medical Alert on Latex products. Be prepared to treat allergic reactions
immediately.
Improper operation may cause the internal lithium battery (hereinafter called
battery) to become hot, ignited or possibly explode, and it may lead to decreased
battery capacity. It is necessary to read the user manual instructions and warning
messages carefully.
Do not touch accessible contacts of electrical equipment and the patient
simultaneously.
This device is not suitable for intra-cardiac use or direct cardiac contact.
The system shall not be serviced or maintained while in use during an exam.
Install the system according the EMC guidance provided in Chapter 14.
Do not stack the system on other electronic equipment.
The use of transducer and connecting cable not supplied by EDAN may result in
increased emissions or decreased immunity of the equipment.
Refer to Chapter 14 for recommended separation distances from other equipment,
including portable and RF communication devices.
The power adapter is used to isolate the system from main power. Position the
system so that it is easy to disconnect the device.
No modification of this equipment is allowed.
The system should be maintained regularly, at least annually, by a qualified
technician who has adequate training, knowledge and experience. That person
should be familiar with the Service Manual (P/N: 01.54.002483), available from
your Edan representative.
Keep non-medical equipment out of the vicinity of the patient. (1.5m/6ft.)
Use of an extension cord or multi-socket outlet setup to provide power to the

Acclarix AX4 Diagnostic Ultrasound System User Manual Safety
- 7 -
ultrasound system or to the system’s peripheral devices, may compromise the
system grounding and cause the system to exceed current leakage limits.
SHOCK HAZARD –Do not connect non-isolated electrical equipment to the same
circuit being used to power the system.
Edan recommends the use of isolated connectors on any electrical equipment
attached to the system, and/or using isolation transformers that comply with
IEC60601-1 to power that electrical equipment.
Always use sterile technique during a biopsy procedure. Sterilize the needle
guide assembly between uses.
Use a sterile needle with each use.
Always confirm the IMT is correctly traced prior to entering the IMT result into the
report.
The system may be interfered with by other equipment, even if that other
equipment complies with CISPR EMISSION requirements.
The system cannot be used together with high-frequency surgical equipment.
Transducer Warnings
To avoid infection, always use protective gloves when cleaning or disinfecting
Read and follow all manufacturer instructions for disinfection agents.
To avoid infection, ensure that expiration date of the disinfecting solution has not
passed.
Disinfect the transducer after each intra-cavity or intra-operative procedure. Use a
new sterile sheath for each such procedure.
Use a pyrogen-free transducer sheath for intra-operative procedures.
The system is not intended to come into contact with the central nervous system
and the central cardiovascular system.
Unplug the transducer from the system prior to cleaning or disinfecting.
Do not immerse the transducer beyond the point indicated in Figure 6-2.
Do not allow the transducer connector to get wet.
2.2 Cautions
The system contains no user serviceable components other than the battery. Do
not remove any covers.
Excessive dust and dirt could clog internal airflow and cause overheating. Do not
use in a dusty environment.
Do not use a battery that leaks, emits an odor, appears deformed, or discolored.
Immediately replace it with a new Edan-supplied battery and dispose of the old
battery according to local regulations. Replace a battery that has reached the end

Acclarix AX4 Diagnostic Ultrasound System User Manual Safety
- 8 -
of its service life.
Use care when storing or disposing of batteries. Do not allow the leakage from one
battery to come in contact with other batteries. Batteries (including button cell on
the main board) are hazardous waste. Do not dispose of them together with
household garbage. At the end of their life hand the batteries over to the
applicable collection points for the recycling of waste batteries. Inappropriate
disposal of waste may contaminate the environment.
Inspect the system regularly, at least weekly. Before use, ensure there is no visible
evidence of damage to the equipment, cables, and transducers. If a component is
damaged, replace it before use.
Do not use in locations subject to vibration.
Read and understand the section A1.2 Ultrasound Safety and the ALARA
Principle of Advanced User Manual before using the system. Do not expose a
patient to ultrasound energy longer than clinically reasonable.
Practice ALARA principle when operating ultrasound system. Minimize the
acoustic power without compromising the image quality.
Do not use in the presence of a flammable anesthetic.
The system generates radio frequency energy, which may cause interference with
other devices in the vicinity. If interference is suspected, try re-orienting or
relocating the equipment.
The use of electrosurgical units or other devices that generate radio frequency
interference may cause image distortion or other malfunctions.
During long term storage, the battery should be charged at least once every 3
months to ensure battery capacity.
The system should only be used by a qualified physician or allied health
professional for ultrasound evaluations.
Use only Edan supplied or recommended parts and accessories.
Verify measurement results prior to entering them into a report.
Contact your local distributor or Edan Service if there is excessive noise from the
system speaker or fans.
Please read and understand cleaning instructions prior to use.
Please read and understand maintenance instructions prior to use.
Please read and understand instructions for system operation prior to use.
Studies stored on the system hard drive should be archived regularly. The system
is not intended for long term storage of patient information. Confirm successful
archiving before deleting a study from the hard drive.
Ensure that the system vents are clear and unobstructed.
Confirm patient identification information prior to storing or printing any exam

Acclarix AX4 Diagnostic Ultrasound System User Manual Safety
- 9 -
information.
If you have any questions about maintenance, technical specifications, or system
functionality, please contact your local distributor or Edan Service at:
[email protected]
Ultrasound images occasionally have artifacts, and should only be used as one
part of an overall clinical assessment.
To avoid electrical shock, turn off and disconnect the device from the AC power
source before cleaning and disinfecting.
The device and accessories are to be disposed of according to local regulations
after their useful lives. Alternatively, they can be returned to the dealer or the
manufacturer for recycling or proper disposal.
The packaging is to be disposed of according to local or hospital’s regulations;
otherwise, it may cause environmental contamination. Place the packaging at a
location that is inaccessible to children.
The system does not need calibration as part of routine maintenance.
Transducer Cautions
Do not use disinfection agents beyond their expiration date.
Do not use sterile sheaths beyond their expiration date.
Inspect the transducer connector, cable, and head periodically. Do not use if there
is evidence of excessive wear or damage.
Do not operate the transducer to temperatures in excess of 40°C or store the
transducer in temperatures in excess of 55°C.
Do not kink or pull on the transducer cable.
Broken or bent connector pins can cause image artifacts. Do not use a transducer
with broken or bent pins.
Properly dispose of used cleaning agents or disinfectants according to your
hospital's regulations.
Network Security Cautions
Keep your ultrasound system safe to protect the patient information and data from
being modified, damaged or disclosed caused by unauthorized disassembly.
Always ensure the privacy of patient information and data displayed/stored in the
ultrasound system or exported to external storage devices.
The software upgrade can only be performed by EDAN-qualified service
professionals with upgrade files of known provenance. Confirm that the system
boots to imaging after an upgrade.
Make sure the ultrasound system is used under secure network environment, and
all the approved devices connecting with the ultrasound system are physically
secure.

Acclarix AX4 Diagnostic Ultrasound System User Manual Safety
- 10 -
Anti-virus measures such as USB device virus scanning should be carried out
prior to using the USB flash drive.
Do not connect an USB device with unknown provenance to the ultrasound
system.
When the ultrasound system is returned for maintenance, disposed of, or removed
from the medical institution for other reasons, ensure all patient data are removed
from the ultrasound system.
NOTE:
The pictures and interfaces in this manual are for reference only.
Federal Communications Commission (FCC) Statement:
This device complies with Part 15 of the FCC Rules. Operation is subject to the
following two conditions:
This device may not cause harmful interference, and
This device must accept any interference received, including interference that
may cause undesired operation.

Acclarix AX4 Diagnostic Ultrasound System User Manual Getting Started
- 11 -
3 Getting Started
3.1 System Configuration
The system is shipped with the following components:
1 main unit
1 rechargeable lithium battery
1 AC adapter
1 power cord
1 bottle of coupling gel
1 basic user manual and 1 advanced user manual
The following options are also available (please see the Order ListAppendix for details)
Transducers: C5-2Q, L12-5Q, E8-4Q, MC8-4Q, L17-7SQ, C5-2MQ, P5-1Q, MC9-3TQ.
1 Trolley MT-807
Footswitch
Suitcase
Multi-Transducer Connector (MTC)
Needle Guide Bracket Kit
Model
Name
Description
BGK-C5-2
BGK-C5-2Needle Guide Bracket Kit
For use with the C5-2Q,
Supports: 16G, 18G, 20G, 22G
BGK-L40UB
BGK-L40UB Needle Guide Bracket Kit
For use with the L12-5Q,
Supports: 16G, 18G, 20G, 22G
BGK-CR10UA
BGK-CR10UA Needle Guide Bracket
Kit
For use with the E8-4Q,
Supports: 16G
BGK-R15UB
BGK-R15UB Needle Guide Bracket Kit
For use with the MC8-4Q,
Supports: 16G, 18G, 20G, 22G
Table 3-1 Needle Guide Bracket Kits

Acclarix AX4 Diagnostic Ultrasound System User Manual Getting Started
- 12 -
Supported Peripheral Accessories：
The recommended printers are listed as follows:
Printer Model
Printer Type
Interface
SONY UP-25MD
Color Image
S-Video
SONY UP-D25MD
Color Image
USB
SONY UP-X898MD
B/W Image
USB
HP OfficeJet Pro 251dw
Color Report
USB
HP LaserJet Pro 200 M251n
Color Report
USB
HP Laserjet CP1525n Color
Color Report
USB
HP Deskjet Ink Advantage 2010
Color Report
USB
HP Deskjet 1010 Color
Color Report
USB
HP Deskjet 1510 Color
Color Report
USB
HP LaserJet 400 M401d
B/W Report
USB
HP DeskJet Ink Advantage Ultra 2029
Color Report
USB
HP DeskJet 1112
Color Report
USB
Canon E518
Color Report
USB
Canon iP2780
Color Report
USB
HP LaserJet Pro MFP m126nw
Color Report
USB
EPSON L310
Color Report
USB
HP DeskJet 1050
Color Report
USB
HP DeskJet 2050
Color Report
USB
HP LaserJet M252n
Color Report
USB
Table 3-2 Printer List
Many other printers may also work with Acclarix systems. To check if your printer
works, connect it to the system, go to Set-up->Store/Print, and click the Add
button. Once it is added, confirm correct operation by clicking the Test button.
If that does not work, you may need to download a printer ppd file from the printer
supplier. In that case download the ppd file to your local computer, and then copy it
to a USB stick inside a directory named “ppd”. Insert that USB stick into the Acclarix
system along with the printer and try again. Most, but not all, printers will work with
the Acclarix systems. A list of printers that should be compatible can be found at
https://developers.hp.com/hp-linux-imaging-and-printing/supported_devices/index,
or at http://gimp-print.sourceforge.net/p_Supported_Printers.php.
WARNING
Only the recommended printers listed above are verified by EDAN. Therefore, it is
suggested to only use these printers. Use of other printers should comply with IEC 60950
or standard IEC 60601-1. Edan is not responsible for the accuracy of other printers.

Acclarix AX4 Diagnostic Ultrasound System User Manual Getting Started
- 13 -
The ultrasound system supports the following external DVD drives: SAMSUNG
SE-218GN, SAMSUNG SE-208GN, LENOVO DB75, ASUS SDRW-08D2S-U,
LITEON eBAU108-11 and PIONEER DVR-XU01C.
The system supports the following DVD disks: Philips CD-R 700MB 80min 52x,
Sony CD-RW 700MB 1x-4x,Sony DVD-RW 4.7GB 120min 2x/1x,
Verbatim DVD+RW 4.7GB 120min 4x.
Note: Only support DVD disk single burning.
3.2 System Overview
Figure 3-1Appearance of the System
No.
Name
Description
1
Monitor
Display the images and parameters during scanning.
2
Touch Screen
Use to control operation and activate functions
3
Control panel
Use to control the operation
4
Handle
Used for carrying the system
10
1
2
3
4
3
5
6
7
8
9
3