EDAN INSTRUMENTS DUS 6 User manual

EDAN INSTRUMENTS, INC.
Digital Ultrasonic Diagnostic
Imaging System
Manual Ver: 1.4
Release Date: Jan. 2010
Part Number: MS1R-102299-1.4

II
Copyright
© Copyright EDAN INSTRUMENTS, INC. 2008-2010. All rights reserved.
Statement
This manual will help you understand the operation and maintenance of the product better. It is
reminded that the product shall be used strictly complying with this manual. User’s operation
failing to comply with this manual may result in malfunction or accident for which Edan
Instruments, Inc. (hereinafter called EDAN) can not be held liable.
EDAN owns the copyrights of this manual. Without prior written consent of EDAN, any
materials contained in this manual shall not be photocopied, reproduced or translated into other
languages.
Materials protected by the copyright law, including but not limited to confidential information
such as technical information and patent information are contained in this manual, the user shall
not disclose such information to any irrelevant third party.
The user shall understand that nothing in this manual grants him, expressly or implicitly, any
right or license to use any of the intellectual properties of EDAN.
EDAN holds the rights to modify, update, and ultimately explain this manual.
Responsibility of the Manufacturer
EDAN only considers itself responsible for any effects on safety, reliability and performance of
the equipment if:
Assembly operations, extensions, re-adjustments, modifications or repairs are carried out by
persons authorized by EDAN, and
The electrical installation of the relevant room complies with international standards, and
The equipment is used in accordance with the instructions for use.
Upon request, EDAN may provide, with compensation, necessary circuit diagrams, and other
information to help qualified technician to maintain and repair some parts, which EDAN may
define as user serviceable.
Using This Guide
This guide is designed to give key concepts on safety precautions.
P/N: MS1R-102299-1.4

III
WARNING :
A WARNING label advises against certain actions or situations that could result in personal
injury or death.
CAUTION :
A CAUTION label advises against actions or situations that could damage equipment, produce inaccurate data,
or invalidate a procedure.
NOTE:
A NOTE provides useful information regarding a function or a procedure.
Revision History
Date ECO# Version Description
2008/08/05 1.0 1st edition
2009/04/24 ECO-DUS -9003 1.3
Added the 3-Aixs (LWH) method, inputting focus, DICOM
function, file browsing, file sending functions, and
transducer power values.
Revised the preface and contact information, the ranges
of the image parameters and the Cleaning and
Disinfecting information.
Added two silicone pads.
2010/01/04 ECO-DUS-9009 1.4
Added two formats of files: AVI and FRM;
Add the function of moving a comment or a body mark;
Added a cable holder;
Added a reference line in the B mode;
Added the magnification function when freezing the
system;
Added the introduction to the guide line calibration;
Added the breakstone guide function;
Added measurement procedures of every supported
obstetrical items, displaying four growth curves of
obstetrical results and more information of obstetrical
reference formulas;
Added detailed information of presetting a report printer;
Added glossary table;
Revised the gain and dynamic range.

IV
Table of Contents
Chapter 1 Introduction .................................................................................................................... 1
1.1. Intended Use..................................................................................................................... 1
1.2. Features ............................................................................................................................ 1
1.3. Model ............................................................................................................................... 2
1.4. Contraindication............................................................................................................... 2
1.5. General Safety Precaution Information............................................................................ 2
1.5.1. General Information................................................................................................ 2
1.5.2. Biohazard Considerations ....................................................................................... 3
1.5.3. Electrical Safety ...................................................................................................... 3
1.6. Labeling Symbols............................................................................................................. 6
Chapter 2 System Overview............................................................................................................ 8
2.1. Appearance....................................................................................................................... 8
2.1.1. Front Panel ..............................................................................................................8
2.1.2. Rear Panel ............................................................................................................. 9
2.1.3. Right View ............................................................................................................ 10
2.2. Configuration ................................................................................................................. 11
2.2.1. Standard Configuration ......................................................................................... 11
2.2.2. Options ..................................................................................................................11
Chapter 3 Transportation and Storage........................................................................................... 13
3.1. Moving the System ........................................................................................................ 13
3.2. Storage............................................................................................................................ 13
3.3. Transportation ................................................................................................................ 13
Chapter 4 Installation Instructions ................................................................................................ 14
4.1. Environmental Requirements......................................................................................... 14
4.2. Unpacking Inspection..................................................................................................... 14
4.3. Connecting Procedure .................................................................................................... 14
4.4. Connecting a Cable Holder ............................................................................................ 14
4.5. Sticking Silicone Pads.................................................................................................... 15
4.6. Connecting or Disconnecting Transducers..................................................................... 16
4.7. Rear Panel Connections ................................................................................................. 17
Chapter 5 System Control ............................................................................................................. 21
5.1. Powering On/Off the Device.......................................................................................... 21
5.2. Examining ...................................................................................................................... 22
5.3. Screen Layout................................................................................................................. 22
5.4. Control Panel.................................................................................................................. 23
5.4.1. Trackball................................................................................................................ 23
5.4.2. “0~9” Numeric Keys............................................................................................. 24
5.4.3. Alphabetic Keys .................................................................................................... 24
5.4.4. Function Controls.................................................................................................. 24
5.4.5. Comment Function................................................................................................ 27

V
5.4.6. Body Mark Function ............................................................................................. 29
5.4.7. Adjustment Controls ............................................................................................. 31
5.4.8. Imaging Functions................................................................................................. 33
5.4.9. Additional Control Functions................................................................................ 35
5.5. Menu .............................................................................................................................. 35
5.6. Dialog Box Operation .................................................................................................... 37
5.7. Presetting........................................................................................................................ 38
5.7.1. Entering and Exiting ............................................................................................. 38
5.7.2. Displaying / Modifying the Preset Parameter ....................................................... 38
5.7.3. General Presetting ................................................................................................. 39
5.7.4. Presetting Examination ......................................................................................... 41
5.7.5. Presetting Formula ................................................................................................ 42
5.7.6. Presetting Post Processing..................................................................................... 44
5.7.7. Editing Comment Library ..................................................................................... 46
5.7.8. Presetting Data ...................................................................................................... 47
5.7.9. Presetting DICOM ................................................................................................ 47
5.7.10. Maintenance ........................................................................................................ 48
5.8. Printing........................................................................................................................... 48
Chapter 6 Operation ...................................................................................................................... 50
6.1. Selecting an Examination Type...................................................................................... 50
6.2. Entering New Patient ..................................................................................................... 50
6.3. Entering or Editing Patient Information......................................................................... 50
6.4. Activating a Transducer ................................................................................................. 51
6.5. Selecting an Imaging Mode ........................................................................................... 51
6.6. Measurement and Calculation........................................................................................ 51
6.6.1. Generic Measurements in B Mode........................................................................ 53
6.6.2. Generic Measurements in M Mode....................................................................... 61
6.6.3. General Report ...................................................................................................... 64
6.7. CINE Review ................................................................................................................. 64
6.8. File Management............................................................................................................ 65
6.8.1. Saving Files........................................................................................................... 66
6.8.2. Opening Files ........................................................................................................ 68
6.8.3. Browsing Images................................................................................................... 69
6.8.4. File Manager ......................................................................................................... 70
6.8.5. Sending Files......................................................................................................... 72
6.9. Puncture Function .......................................................................................................... 73
6.9.1. To Select the Angle of Needle Guide Line............................................................ 74
6.9.2. To Display or To Hide the Needle Guide Line...................................................... 75
6.9.3. To Adjust the Needle Guide Line.......................................................................... 75
6.9.4. Reference Line ...................................................................................................... 76
6.10. Breakstone Guide ........................................................................................................ 76
Chapter 7 Obstetric Measurement and Calculation ...................................................................... 77
7.1. Abbreviations ................................................................................................................. 77
7.2. Obstetric Measurement and Calculation ........................................................................ 77

VI
7.3. Fetus Growth Measurement ........................................................................................... 78
7.3.1. GS.......................................................................................................................... 79
7.3.2. CRL ....................................................................................................................... 79
7.3.3. BPD....................................................................................................................... 79
7.3.4. HC ......................................................................................................................... 80
7.3.5. AC ......................................................................................................................... 80
7.3.6. FL .......................................................................................................................... 81
7.3.7. AFI ........................................................................................................................ 81
7.3.8. TAD....................................................................................................................... 81
7.3.9. APAD .................................................................................................................... 82
7.3.10. CER..................................................................................................................... 82
7.3.11. FTA...................................................................................................................... 83
7.3.12. HUM ................................................................................................................... 83
7.3.13. OFD..................................................................................................................... 83
7.3.14. THD..................................................................................................................... 84
7.4. EDC Calculation ............................................................................................................ 84
7.4.1. EDC Calculation by Entering LMP ...................................................................... 84
7.4.2. EDC Calculation by Entering BBT....................................................................... 85
7.5. EFW Calculation............................................................................................................ 86
7.5.1. Select a Formula in Preset..................................................................................... 86
7.5.2. Measurement Items ............................................................................................... 86
7.6. Results............................................................................................................................ 87
7.6.1. Growth Curve........................................................................................................ 87
7.6.2. Obstetric Report .................................................................................................... 89
7.7. Others ............................................................................................................................. 90
Chapter 8 Cardiology Measurement and Calculation ................................................................... 91
8.1. M-mode Cardiac Measurement and Calculation............................................................ 91
8.1.1. LV.......................................................................................................................... 96
8.1.2. Mitral Valve........................................................................................................... 98
8.1.3. Aortia..................................................................................................................... 99
8.1.4. LVMW, LVMWI ................................................................................................. 100
8.2. B-mode Cardiac Measurement and Calculation .......................................................... 100
8.2.1. LV........................................................................................................................ 105
8.2.2. RV (Right ventricle internal diameter)................................................................ 107
8.2.3. PA (Aortic Pulmonary Artery)............................................................................. 107
8.3. Cardiac Report ............................................................................................................. 108
8.4. Others ........................................................................................................................... 109
Chapter 9 Gynecology Measurement and Calculation................................................................ 110
9.1. Measurement and Calculation...................................................................................... 110
9.1.1. UT ........................................................................................................................111
9.1.2. Endo .....................................................................................................................111
9.1.3. OV-V ....................................................................................................................111
9.1.4. FO........................................................................................................................ 112
9.1.5. CX-L ................................................................................................................... 112

VII
9.1.6. UT-L/CX-L.......................................................................................................... 112
9.2. Gynecologic Report ..................................................................................................... 112
9.3. Others ........................................................................................................................... 113
Chapter 10 Small Parts Measurement and Calculation............................................................... 114
10.1. Measurement and Calculation................................................................................... 114
10.2. Small Parts Report..................................................................................................... 115
10.3. Others ........................................................................................................................ 115
Chapter 11 Urology Measurement and Calculation.................................................................... 116
11.1.Measurement and Calculation...................................................................................... 116
11.2.Urologic Report............................................................................................................ 117
11.3.Others ........................................................................................................................... 118
Chapter 12 Orthopedics Measurement & Calculation ................................................................ 119
12.1. Measurement and Calculation................................................................................... 119
12.2. Orthopedics Report ................................................................................................... 119
12.3. Others ........................................................................................................................ 120
Chapter 13 Inspection and Maintenance ..................................................................................... 121
13.1. Daily Checklist.......................................................................................................... 121
13.2. Cleaning and Disinfection......................................................................................... 121
13.2.1. System Surface Cleaning ................................................................................. 123
13.2.2. Probe and Probe Holder Cleaning and Disinfection ........................................ 123
13.2.3. Needle Guide Cleaning and Disinfecting......................................................... 126
13.2.4. Trackball Cleaning ........................................................................................... 126
13.2.5. Disinfectants..................................................................................................... 127
13.3. Maintenance .............................................................................................................. 127
Chapter 14 Troubleshooting........................................................................................................ 129
14.1. Checkup..................................................................................................................... 129
14.2. Troubleshooting ........................................................................................................ 129
Chapter 15 Warranty and Service Policy .................................................................................... 130
15.1. Warranty...................................................................................................................... 130
15.2. Service Policy.............................................................................................................. 130
Appendix I: Specifications.......................................................................................................... 132
A1.1: Electrical Safety Classifications................................................................................. 132
A1.2: Standards Compliance................................................................................................ 132
A1.3: Power Supply ............................................................................................................. 132
A1.4: Machine Specifications .............................................................................................. 133
A1.5: General Technical Specifications ............................................................................... 133
A1.6: Probe Specifications................................................................................................... 134
A1.7: Operating, Storage and Transportation Environment................................................. 135
A1.7.1. Operating Environment:................................................................................... 135
A1.7.2. Storage and Transportation Environment:........................................................ 135
Appendix II: Ultrasound Intensity and Safety ............................................................................ 136

VIII
A2.1: Ultrasound in Medicine.............................................................................................. 136
A2.2: Ultrasound Safety and the ALARA Principle ............................................................ 136
A2.3: Probe Acoustic Output Parameters List ..................................................................... 138
A2.3.1 : Test of Probe C363-1 ..................................................................................... 138
A2.3.2 : Test of Probe L743/E743 ............................................................................... 139
A2.3.3 : Test of Probe C321......................................................................................... 140
A2.3.4 : Test of Probe E613 ......................................................................................... 141
A2.3.5 : Test of Probe C343-1 ..................................................................................... 142
A2.4: Transducer Power Values ........................................................................................... 143
A2.5: Low Output Summary Table ...................................................................................... 149
Appendix III: Obstetrical References.......................................................................................... 150
A3.1: Application Table of Obstetrical Reference Formulas ............................................... 150
A3.2: GS............................................................................................................................... 151
A3.3: CRL ............................................................................................................................ 153
A3.4: BPD............................................................................................................................ 155
A3.5: HC .............................................................................................................................. 158
A3.6: AC .............................................................................................................................. 159
A3.7: FL ............................................................................................................................... 161
A3.8: FTA ............................................................................................................................ 163
A3.9: HUM .......................................................................................................................... 165
A3.10: CER.......................................................................................................................... 165
A3.11: THD.......................................................................................................................... 165
A3.12: Estimated Fetal Weight ............................................................................................ 165
Appendix IV: Measurement Accuracy ........................................................................................ 166
Appendix V: EMC Information-Guidance and Manufacture’s Declaration ............................... 167
Appendix VI: Order List ............................................................................................................. 171
Appendix VII: Glossary .............................................................................................................. 172

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Chapter 1 Introduction
1.1. Intended Use
The DUS 6 Digital Ultrasonic Diagnostic Imaging System is intended for diagnostic ultrasound
imaging analysis in gynecology rooms, obstetrics rooms, examination rooms, intensive care units,
and emergency rooms. The DUS 6 is intended for use by or on the order of a physician or
similarly qualified health care professional for ultrasound evaluation of Fetus; Abdomen;
Pediatrics; Small Organ; Neonatal head; Cardiology; Peripheral Vessel; Musculo-skeleton (both
Conventional and Superficial); Urology (including prostate); Transrecta and Transvagina.
1.2. Features
This portable device, Digital Ultrasonic Diagnostic Imaging System (DUS 6), is a high-resolution
linear/convex scanning diagnostic apparatus.
Applied technologies:
Tissue Specific Imaging (TSI), Tissue Harmonic Image (THI), Digital Beam-Forming (DBF),
Dynamic Receiving Focusing (DRF), Real-time Dynamic Aperture (RDA), Dynamic Frequency
Scanning (DFS), and Dynamic Apodization.
Display modes:
B, B+B, 4B, B+M, and M.
Measurement and calculation functions:
B-mode generic measurement and calculation: Distance, circumference, area, volume, ratio, %
stenosis, and angle;
M-mode generic measurement and calculation: Time, slope, and heart rate.
File management:
It supports local disk and removable disk storage. USB 1.1 interface enables fast image uploading
to your computer in the real-time mode. It has a 56 MB storage capacity.
Operation:
The folding keyboard designed with trackball is easy and convenient for various types of
operation.
In addition, 10" non-interlaced progressive display and diverse probes are adopted to provide a
clear and stable image.

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1.3. Model
DUS 6
1.4. Contraindication
The equipment is not applicable to the diagnosis of the pneumatic organs that contain gas
such as lung, stomach, intestines, etc.
It is recommended not to examine the parts with wounds or acute inflammation to avoid
cross infection.
Patients in the following situations are not allowed to be examined with E613 probe: vaginal
infection (such as trichomonal vaginitis, colpomycosis, venereal disease etc.), the unmarried,
vagina deformity, menstrual period, postmenopausal vagina atrophy, difficulty in per vagina
ultrasonic examination, colporrhagia, Pyrilamine placenta previa, etc.
1.5. General Safety Precaution Information
1.5.1. General Information
WARNING :
This equipment is not intended for treatment.
CAUTION :
1. Federal (U.S.) law restricts this device to sale by or on the order of a physician.
2. The pictures and interfaces in this manual are for reference only.
NOTE:
This equipment is not intended for home use.
The reliability of the device and the safety of operators and patients are considered during
product design and production. The following safety and preventive measures should be carried
out:
1. The device should be operated by qualified operators or under their instructions.
2. DO NOT alter parameters of the device at will. If it is necessary, please consult EDAN or
authorized representatives for service.
3. The device has already been adjusted to its optimum performance. DO NOT adjust any
pre-set control or switch, unless it is listed in this manual.
4. If the device breaks down, please shut down the machine immediately and contact EDAN or

DUS 6 Digital Ultrasonic Diagnostic Imaging System User Manual
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authorized representatives.
5. Only accessories supplied or recommended by EDAN can be used. Otherwise, the
performance and electric shock protection can not be guaranteed. If electrical or mechanical
equipment from other companies need to be connected to the device, please contact EDAN or
authorized representatives before connection.
6. EXPLOSION HAZARD-Equipment is not suitable for use in the presence of a flammable
anesthetic mixture with air or with oxygen or nitrous oxide.
1.5.2. Biohazard Considerations
WARNING :
1. This device is not suitable for intracardiac use or direct cardiac contact.
2. For neonatal head imaging, EDAN recommends that you exercise special care
during neonatal cephalic scanning to avoid possible damage to the posterior region
of the eye. The ultrasound energy emitted by the transducer easily penetrates the
fontanels of the infant.
3. EDAN makes every effort to manufacture safe and effective transducers. You must
take all necessary precautions to eliminate the possibility of exposing patients,
operators, or third parties to hazardous or infectious materials. These precautions
should be considered in the use of any application that may indicate the need for
such care, and during endocavity scanning; or when scanning patients with open
wounds.
Ultrasound may be harmful to human body. This device should be used for valid reasons,
for the shortest period of time, and at the lowest mechanical and thermal indices necessary to
produce clinically acceptable images. According to the ALARA (As Low As Reasonably
Achievable) principles, acoustic output should be set to the lowest level required to satisfactorily
perform the examination. Long time exposure should be avoided. For the parameters of sound
output, please refer to appendix A.
The DUS 6 complies with the requirements of applicable International Electrotechnical
Commission (IEC) standards in terms of safety and acoustic output levels.
1.5.3. Electrical Safety
WARNING :
1. To ensure grounding reliability, only connect the system to a hospital-grade power

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receptacle.
2. The AC power connector plug for the ultrasound system is a three-prong grounded
plug and should never be adapted to any two-prong (non-grounded) outlet, either by
modifying the plug or by using an adapter.
3. To avoid electrical shock, never modify the ultrasound system’s AC power circuits.
To ensure grounding reliability, connect the system only to an equivalent outlet.
4. SHOCK HAZARD-Do not attempt to connect or disconnect a power cord with wet
hands. Make certain that your hands are clean and dry before touching a power
cord.
5. The equipment should be installed by a qualified service engineer. Do not try to
access the interior of the main unit. Only authorized service personnel could remove
the unit cover.
6. Before use, you must make sure that there is no visible evidence of damage on the
equipment, cables and probes which may affect patient safety or diagnostic
capability. The recommended inspection interval is once per week or less. If damage
is evident, replacement is recommended before use.
7. Equipment connected to the DUS 6 and located in the patient zone must be
powered from a medically-isolated power source or must be a medically-isolated
device. Equipment powered from a non-isolated source can cause your system to
exceed leakage current limits. Enclosure leakage current created by an accessory or
device connected to a non-isolated outlet may add to the enclosure leakage current
of the imaging system.
8. Use an extension cord or multi-socket outlet setup to provide power to the
ultrasound system or to the system’s peripheral devices, may compromise the
system grounding and cause your system to exceed leakage current limits.
9. To avoid electrical shock and damage to the system, turn off and disconnect the
device from the AC power source before cleaning and disinfecting.
10. When more than one medical device is connected to the patient, leakage current of
the devices is summed together. Take caution.
11. Don’t touch the signal input or output connector and the patient simultaneously.
12. Periodically have the integrity of the system ground checked by a qualified service
engineer.

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CAUTION :
1. To avoid the possibility of electrostatic shock and damage to the system, avoid using
aerosol spray cleaners on the monitor screens.
2. DO NOT use spray cleaners on the system, as this may force cleaning fluid into the
system and damage electronic components. It is also possible for the solvent fumes
to build up and form flammable gases or damage internal components.
3. DO NOT use any fluid onto the system surface, as fluid seepage into the electrical
circuitry may cause excessive leakage current or system failure.
4. To ensure proper grounding and leakage current levels, it is the policy of EDAN to
have an authorized EDAN representative or an EDAN approved third party performs
all on-board connections of documentation and storage devices to the DUS 6.
5. 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. Batteries are hazardous waste. Do not dispose them
together with house-hold garbage. At the end of their life hand the batteries over to
the applicable collection points for the recycling of waste batteries. For more detailed
information about recycling of this product or battery, please contact your local Civic
Office, or the shop where you purchased the product.
NOTE:
Please use the standard power cord as the input line of the network power supply for the
adapter to reduce risk.
Electromagnetic Compatibility (EMC)
Operating the DUS 6 in close proximity to sources of strong electromagnetic fields, such
as radio transmitter stations or similar installations may lead to interference visible on the
monitor screen. However, the device has been designed and tested to withstand such
interference and will not be permanently damaged.
EMI Limitations
Ultrasound machines are susceptible to Electromagnetic Interference (EMI) from radio
frequencies, magnetic fields, and transients in the air of wiring. Ultrasound machines also
generate EMI. The DUS 6 complies with limits as stated on the EMC label. However, there is no
guarantee that interference will not occur in a particular installation.
Possible EMI sources should be identified before the unit is installed.
Electrical and electronic equipment may produce EMI unintentionally due to one of the following
defects:
¾High frequency electrotome

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¾Transformer
¾Defibrillator
¾Wireless LAN equipment
¾Medical lasers
¾Scanners
¾Cauterizing guns
¾Computers
¾Monitors
¾Fans
¾Gel warmers
¾Microwave ovens
¾Light dimmers
¾Portable phones
The presence of a broadcast station or broadcast van may also cause interference.
If you find strong interference shows on the screen, please check the sources.
1.6. Labeling Symbols
Descriptions of symbols of the device are shown in table 1-1.
No. Symbol Definition
1 Serial Number
2 P/N Part Number
3 Date of Manufacture
4 Manufacturer
5 Consult Instructions for Use
6 Symbol for “Caution”
7 Biological Risks
8
It indicates that the equipment should be sent to special agencies
according to local regulations for separate collection after its useful life.
9
It indicates that the equipment should be sent to special agencies
according to local regulations for separate collection after its useful life and
that this equipment is put on the market after 13 August 2005.

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10
General Symbol for Recovery / Recyclable
11 Federal (U.S.) law restricts this device to sale by or on the order of a
physician.
12 Authorized Representative in the European Community
13
The symbol indicates that the device complies with the European Council
Directive 93/42/EEC concerning medical devices.
14 Type B, Applied Part
15 Alternating Current (a.c.)
16 ON (AC power supply)
17 OFF (AC power supply)
18
Equipotentiality
19 VGA
VGA output, External Monitor
20 Fuse
21 Probe socket
22 Net work port
23
Foots witch
To identify a foot switch or the connection for a foot switch.
24 Protective earth (ground)
25 Recording on an information carrier
26 Trademark
27 USB (Universal Serial Bus) Connection
28 Dangerous voltage
29
Variability, for rotating movement
Rotate clockwise to increase the value, and counterclockwise to decrease
the value.
30
Variability
Adjust right to increase the value, and left to decrease the value.
Table 1-1 Descriptions of Symbols

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Chapter 2 System Overview
2.1. Appearance
2.1.1. Front Panel
Figure 2-1 Front Panel Schematic Diagram
1. Probe holders
2. Display screen
3. Contrast adjustment knob
4. Brightness adjustment knob
5. Acoustic power adjustment knob
6. Control panel
7. Power switch
8. Trough for the coupling gel
9. Handle
1
3
4
5
2
6
7
8
9 1
2
3
4
5
6
9
8
7

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2.1.2. Rear Panel
Figure 2-2 Rear Panel Schematic Diagram
1 Footswitch port
2 Network port
3 Fuse
4 Power supply input port
5 Equipotential earth terminal
6 VGA output port
7 Remote port
8 Video output port
CAUTION :
To have good aeration performance and be able to operate normally, please don’t cover
or plug the air fan or heat dissipation orifice partly or wholly by using any object.
Air Fan:
Heat emission fan
7
8
1
2
3
4
5
6
1
2
3
4
5
8
7
6

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2.1.3. Right View
Figure 2-3 Right View Schematic Diagram
Peripheral ports:
2 transducer ports (dual sockets)
2 USB ports
1 probe holder (for two probes)
Transducer PortsProbe Holder

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2.2. Configuration
2.2.1. Standard Configuration
1 DUS 6 main unit
1 convex array transducer: C363-1
1 power cord (European Standard)
1 ground wire
1 probe holder
1 cable holder
2 pieces of fuse, φ5×20, T1.6AL/250V
1 bottle of coupling gel 250mL
1 user manual
2 packing lists
2 silicone pads
2.2.2. Options
The Digital Ultrasonic Diagnostic Imaging System supports the following options:
(1) Transducers
Convex array transducer: C343-1;
Linear array transducer: L743;
Endorecta transducer: E743;
Endocavity transducer: E613;
Micro-convex array transducer: C321.
(2) Others
Ultrasonic Imaging Management System software specifications
Operating system: support WINDOWS XP, and WINDOWS VISTA.
Video printer and USB printer are as shown in table 2-1.

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Options Recommended Models
Video printer SONY UP-895MD, SONY UP-897MD, MITSUBISHI P93W
USB printer
HP DeskJet D2368, HP DeskJet D2468, HP DeskJet D2568
HP DeskJet D4368, HP LaserJet P2015, HP LaserJet P2035
Table 2-1 Printers
Video printer output: 110 mm× 82 mm; USB printer output: A4 paper, 210 mm× 297 mm.
Puncture frames
Model Name Description
BGK-CR60 Needle Guide Bracket Kit For the R60 probe, 4 vessels: 14G, 18G, 20G, 22G
BGK-CR40 Needle Guide Bracket Kit For the R40 probe, 4 vessels: 14G, 18G, 20G, 22G
BGK-CR20 Needle Guide Bracket Kit For the R20 probe, 4 vessels: 14G, 18G, 20G, 22G
BGK-CR10 Needle Guide Bracket Kit For the R10 probe, 4 vessels: 14G, 18G, 20G, 22G
BGK-LA43 Needle Guide Bracket Kit For the L43 probe, 4 vessels: 14G, 18G, 20G, 22G
Table 2-2 Needle Guide Bracket Kits
The puncture frame of BGK-CR60 is as shown in figure 2-4.
Figure 2-4 Puncture Frame of BGK-CR60
DICOM 3.0
Single-pedal footswitch
MT-802 Mobile trolley
The mobile trolley has a compact and mobile console with four wheels and four brakes
for safe and convenient transport. It can be assembled or disassembled easily, refer to
MT-802 Trolley Assembling Instruction. The external structure complies with usability
engineering. It has two holders for the probes and one holder for the coupling gel.
Hand carried bag
The bag is portable and it can be carried over the shoulder. It can contain not only the
main unit but also two probes (an array transducer R60/3.5MHz and an endocavity
transducer R10/6.5MHz) and one bottle of coupling gel. It is watertight.
KINGSTON U disk: DT1 G2 (2G) Kingston