MINDRAY
M9 Series and M8 Series Service Manual (Advanced) Rev 25.0
Service Manual
267 Pages
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Page 1
M9/M9T/M9CV/M9GI/M9Vet/ M8/M8CV/M8T/M8GI/M8 Elite
Diagnostic Ultrasound System
Service Manual (Advanced)
Revision 25.0
Table of Contents Table of Contents...i Version Information ...I Intellectual Property Statement ...III Applicability ...III Responsibility of Mindray ...III Warranty Statements ... IV Customer Service Department ... IV Descriptions Committed ... V 1
Safety Precautions ... 1-1 1.1 1.2
Meaning of Signal Words ... 1-1 Symbols ... 1-1 1.2.1 Meaning of Safety Symbols ... 1-1 1.2.2 Warning Labels ... 1-2 1.2.3 General Symbols ... 1-2 1.3 Safety Precautions ... 1-3 1.3.1 Electric Safety ... 1-4 1.3.2 Mechanical Safety ... 1-5 1.3.3 Personnel Safety ... 1-5 1.3.4 Others ... 1-5
2
Product Specifications ... 2-1 2.1
Introduction... 2-1 2.1.1 Intended Use ... 2-1 2.1.2 System Appearance ... 2-1 2.1.3 Trolley Appearance ... 2-10 2.1.4 Peripherals Supported ... 2-13 2.2 Specifications ... 2-14 2.2.1 External Dimensions and Weight ... 2-14 2.2.2 Electric Specifications ... 2-14 2.2.3 Environment Specifications ... 2-15 2.2.4 Monitor Specifications ... 2-15
3
System Installation ... 3-1 3.1
Installation Preparations ... 3-1 3.1.1 Electrical Requirements ... 3-1 3.1.2 Installation Condition ... 3-2 3.1.3 Installation Confirmation ... 3-2 3.2 Unpacking ... 3-2 3.2.1 Unpacking Process ... 3-2 3.2.2 Check ... 3-7 3.3 Installation of Whole Device ... 3-7 3.3.1 Connecting Power Cable ... 3-7 3.3.2 Connecting ECG ... 3-7 3.3.3 Connecting a Ultrasound Probe ... 3-7 3.4 Installing Peripherals ... 3-8 3.4.1 Connecting the Footswitch ... 3-8
i
3.4.2 Connecting/Removing a USB Memory Device... 3-8 3.4.3 Graph/Text Printer... 3-9 3.4.4 Video Printer ... 3-11 3.4.5 Barcode Reader... 3-12 3.5 Wired Network Connection ... 3-17 3.6 System Configuration ... 3-17 3.6.1 Power-on Running ... 3-17 3.6.2 Enter Doppler... 3-17 3.6.3 System Preset ... 3-18 3.6.4 Print Preset ... 3-19 3.6.5 Network Preset ... 3-20 3.6.6 Network Configure ... 3-24 3.6.7 DICOM/HL7 Preset ... 3-30 3.6.8 Security ... 3-32 3.6.9 System Information Verification ... 3-35
4
Product Principle ... 4-1 4.1 4.2
General Structure of Main Unit’s Hardware System ... 4-1 Main Board ... 4-2 4.2.1 Power Supply... 4-3 4.2.2 Backend ... 4-3 4.2.3 Front-end of Main Board ... 4-5 4.3 TR64 Board ... 4-6 4.4 Probe Board ... 4-6 4.5 PHV Power Supply Board ... 4-7 4.6 ECG Unit ... 4-7 4.7 Control Panel... 4-9 4.8 Main Display Unit ... 4-10 4.9 Probe Extension Board ... 4-11 4.10 Audio/Video Transfer Module ... 4-12 4.11 USB HUB Board ... 4-13 4.12 Trolley Power Supply ... 4-13 4.12.1 Connection Board of Trolley Power Supply ... 4-14 4.12.2 AC_DC Power Supply ... 4-14 4.12.3 Management Board of Trolley Battery ... 4-14 4.13 System Power-on Control ... 4-15 4.14 Internal Connection Diagram of Main Unit and Trolley ... 4-17 4.15 Details in Main Unit’s Power-on ... 4-17
5
Checking Performance and Functions ... 5-1 5.1 5.2
Description ... 5-1 Checking System Status ... 5-1 5.2.1 Running Status ... 5-1 5.2.2 Working Condition ... 5-1 5.3 General Check ... 5-2 5.3.1 Check Flow ... 5-2 5.3.2 Check Content ... 5-2 5.4 Functions Checking ... 5-5 5.4.1 Checking Flow ... 5-5 5.4.2 Checking Content ... 5-5 5.5 Performance Test ... 5-11 5.5.1 Test Procedures ... 5-11
ii
5.5.2
6
Test Content... 5-12
Software Installation & Maintenance ... 6-1 6.1 6.2 6.4 6.5
Enter Maintenance ... 6-1 Software Installation/Restoration ... 6-2 Enter Windows ... 6-5 Software Maintenance... 6-6 6.5.1 Log Export ... 6-6 6.6 Data Backup and Storage ... 6-6 6.6.1 Preset Data Management ... 6-6 6.6.2 Patient Data Backup and Restoration ... 6-7 6.7 Introduction on HDD Partition Data ... 6-7
7
Field Replaceable Unit ... 7-1 7.1 7.2
8
Explosive View ... 7-2 Assembly Explosive View... 7-3 7.2.1 Monitor Assembly (A0) ... 7-3 7.2.2 Control Panel Assembly (B0)... 7-5 7.2.3 Main Unit Assembly (C0) ... 7-7 7.2.4 Cables (D0)... 7-12 7.2.5 Accessories (E0)... 7-13 7.2.6 UMT-500 Mobile Trolley (F0) ... 7-15
Structure and Assembly/Disassembly... 8-1 8.1
Structure of the Complete System ... 8-1 8.1.1 Main Unit... 8-1 8.1.2 Mobile Trolley... 8-2 8.2 Main Unit Assembly/Disassembly ... 8-3 8.2.1 Preparation ... 8-3 8.2.2 Battery ... 8-4 8.2.3 Dust-proof Mesh of Main Unit ... 8-5 8.2.4 Network Adaptor ... 8-6 8.2.5 SSD Card... 8-7 8.2.6 Control Panel and Monitor ... 8-8 8.2.7 ECG Assembly... 8-10 8.2.8 Fan ... 8-12 8.2.9 Probe Board Assembly ... 8-12 8.2.10 Machine Board Assembly ... 8-14 8.2.11 Control Panel Assembly ... 8-18 8.2.12 Display (monitor) Assembly ... 8-23 8.3 Trolley Assembly/Disassembly ... 8-27 8.3.1 Preparation ... 8-27 8.3.2 Storage Box ... 8-28 8.3.3 Power Supply Assembly ... 8-29 8.3.4 Trolley Panel Board Assembly ... 8-33 8.3.5 Spring Assembly ... 8-34 8.3.6 Cast-aluminum Base of Trolley Panel ... 8-40 8.3.7 Lifting Column ... 8-42 8.3.8 Trolley Base Assembly ... 8-43 8.3.9 Installation of probe holder ... 8-45 8.3.10 Disassembly of the probe holder ... 8-47 8.3.11 Disassembly of intracavity probe holder ... 8-47
9
Installation of Option Modules ... 9-1 iii
9.1 9.2
Installation of Optional Devices to Software... 9-1 Installation of the Accessory Kits and Optional Devices to Hardware ... 9-3 9.2.1 Storage Tray ... 9-4 9.2.2 Probe Extender Assembly ... 9-4 9.2.3 Audio/Video Extender Assembly ... 9-5 9.2.4 Trolley Installation ... 9-6
10 System Diagnosis and Support... 10-1 10.1 General Status Indicator ... 10-1 10.1.1 Indicators of Control Panel ... 10-1 10.1.2 Status of Whole Machine ... 10-2 10.2 Get Whole Machine Started ... 10-3 10.2.1 Power-on Process of Whole Machine Supplied by AC... 10-4 10.2.2 The Start-up Process of BIOS ... 10-4 10.2.3 Windows Start-up... 10-4 10.2.4 The Start-up of Doppler ... 10-5 10.3 Alarming and Abnormal Information ... 10-7 10.3.1 Power Error... 10-7 10.3.2 Abnormal Voltage of System Power ... 10-9 10.3.3 Abnormal Temperature ... 10-9 10.3.4 Fan Error... 10-10 10.3.5 PHV Error ... 10-10 10.3.6 Other Errors ... 10-11 10.4 Self-test ... 10-11 10.4.1 Self-test Introduction ... 10-11 10.4.2 Operation Procedure of Maintenance Self-test ... 10-12 10.4.3 User Self-test ... 10-16 10.4.4 Test Report ... 10-18
11 Care and Maintenance...11-1 11.1 Overview ... 11-1 11.1.1 Tools, Measurement Devices and Consumables ... 11-1 11.1.2 Routine Maintenance Items ... 11-2 11.2 Cleaning ... 11-3 11.2.1 System Cleaning... 11-3 11.2.2 Peripherals Cleaning ... 11-7 11.3 Check ... 11-7 11.3.1 General Check ... 11-7 11.3.2 System Function Check ... 11-8 11.3.3 Check for Peripherals and Optional Functions ... 11-8 11.3.4 Mechanical Safety Inspection ... 11-9
12 Troubleshooting of Regular Malfunctions... 12-1 12.1 Troubleshooting as the System is Disabled to Power On ... 12-1 12.1.1 Related Modules or Boards ... 12-1 12.1.2 Key Points Supporting Troubleshooting ... 12-1 12.1.3 Troubleshooting as the System is Disabled to Power On ... 12-1 12.2 The System Cannot Perform Troubleshooting ... 12-2 12.2.1 Related Modules or Boards ... 12-2 12.2.2 Key Points Supporting Troubleshooting ... 12-2 12.2.3 The System Cannot Perform Troubleshooting ... 12-3 12.3 Image Troubleshooting ... 12-3 12.3.1 Related Modules or Boards ... 12-3
iv
12.3.2 Key Points Supporting Troubleshooting ... 12-3 12.3.3 Image Troubleshooting ... 12-4 12.4 Troubleshooting Control Panel ... 12-4 12.4.1 Related Modules or Boards ... 12-4 12.4.2 Key Points Supporting Troubleshooting ... 12-4 12.4.3 Troubleshooting Control Panel ... 12-5 12.5 Troubleshooting LCD Display... 12-5 12.5.1 Related Modules or Boards ... 12-5 12.5.2 Key Points Supporting Troubleshooting ... 12-6 12.5.3 Troubleshooting Monitor ... 12-6 12.6 Troubleshooting for ECG Module ... 12-6 12.6.1 Related Modules or Boards ... 12-6 12.6.2 Key Points Supporting Troubleshooting ... 12-6 12.6.3 Troubleshooting for ECG Module ... 12-7
Appendix A
Electrical Safety Inspection ... A-1
Appendix B
Phantom Usage Illustration... B-1
Appendix C
Description of Self-test Test Items ... C-1
v
Version Information Mindray may revise this publication from time to time without written notice. The detailed information is shown below: Version
Release Date
1.0
2013.12.30
Reason for Revision Initial release Add the picture of field replaceable unit in Chapter 7.1;
2.0
2014.1.27
3.0
2014.3.19
4.0
2014.6.12
Change the order number of the speaker and cable in Chapter 7.1; Change the disassembly method of the shield cover of PHV board in Chapter 8.2.10 Add the precaution of the disassembly of the CPU assembly; Update the content of the appendix C.1.25 Update figures in chapter 8.2.7 since a pressure plate is added for ECG cable; Update contents of Z0501 in appendix C.1.25 Change FRU materual No. in Chapter 7; Change iStorage screen picture in section 3.5.5.1;
5.0
2014.9.24
6.0
2015.2.15
Add section 3.5.6 Network Configure; Add in “4-protective grounding impedance” testing applies to M9 portable system with UMT-500Plus trolley (with power supply) only in Appendix A. Add SONY UP-D898MD, UP-X898MD printers in chapter 2.1.4 along with compatibility description. Section 7.1, add the part number of main board and SSD card used for CE M9GI
7.0
2015.5
Section 7.1, change the picture of SSD card Section C.1.27, change the picture of keyboard testing Add M9GI product model
8.0
2015.8
Section 3.5, add the wired network connection information.
11.0
2016.4.7
Section 7, change the wired network connection information.
12.0
2016.5.20
Section 7, the modification of the FRU.
13.0
2016.8.9
Update the labels in 1.2.2. Add M9Vet model. Add 4D and TEE related self-test items in C.1.16 – C.1.19 chapter
14.0
2017.1
Update trolley probe holder part number and add part number of intracavity probe holder in 7.2 chapter Add assembly/disassembly descriptions in 8.3.9 – 8.3.11 for probe holders.
15.0
2017.6
Update Monitor Assembly(eDP screen/FRU), Monitor Assembly(LVDS2eDP/FRU), CPU Module(6100 PC module/eDP output/FRU), CPU Module(6100 PC module/LVDS output/FRU), M9
I
Main Board(eDP output+M.2 port WiFi/FRU), M9 Main Board(M9GI/eDP output+M.2 port WiFi/FRU), Wireless net adapter(M.2 port), iDock51 Audio/Video Extend Module, SSD card FRU, Monitor front cover assembly FRU, control panel assembly FRU in chapter 7.1. Update Audio/Video extend module FRU in chapter 9.2. 16.0
2017.9
Add the FRU number of Russian keyboard.
17.0
2017.12
Change the FRU number of TR64 board in chapter 7.1. 1. Add M8 series product models.
18.0
2017.06
2. Add FRUs. 3. Add anti-virus, Q-Path, EAP network. 1. Update the unpacking information in section 3.2
19.0
2018.09
20.0
2018.10
21.0
2019.01
22.0
2019.7
23.0
2019.09
Change the FRU number of Control Panel Assembly and PC Keyboard in chapter 7.1.
24.0
2020.2
Change the FRU information of CPU module in chapter 7.1.
25.0
2020.3
Update EAP network management; add Windows 10 activation; Change the FRU information in chapter 7.1.
2. Update th screw type in section 8.3.3 1.
Add the lithium-ion Battery FRU
2.
Modify the screwdriver size.
Change the FRU number of Small keyboard assembly(FRU) in chapter 7.1. Change DS6707 to DS4308 in Chapter 2.1.4. Change the FRU number of Main Board, Control panel assembly (FRU) and Silicon keypad in chapter 7.1.
© 2013-2020 Shenzhen Mindray Bio-medical Electronics Co., Ltd. All Rights Reserved.
II
Intellectual Property Statement SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called “Mindray”) owns the intellectual property rights to this Mindray product and this manual. This manual may refer to information protected by copyright, trademark, or patents, and does not convey any license under the intellectual property rights of Mindray or of others. Mindray intends to maintain the contents of this manual as confidential information. Disclosure of the information in this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden. Release, amendment, reproduction, distribution, rental, adaptation, translation or any other derivative work of this manual in any manner whatsoever without the written permission of Mindray is strictly forbidden. is the trademark of Mindray. All other trademarks that appear in this manual are used only for informational or editorial purposes. They are the property of their respective owners.
Applicability This service manual is intended as a guide for technically qualified personnel during service procedures. This service manual describes the product according to the most complete configuration; some of the content may not apply to the specific product you are servicing. If you have any questions, please contact the Mindray Customer Service Department (contact information is below). Do not attempt to service this equipment unless this service manual has been consulted and is understood. Failure to do so may result in personal injury or product damage.
Responsibility of Mindray Contents of this manual are subject to change without prior notice. Please check with the Mindray Customer Service Department for any updates or changes to this manual. All information contained in this manual is believed to be correct as of the date of its publication. Mindray shall not be liable for errors contained herein or for incidental or consequential damages in connection with the furnishing, performance, or use of this manual. Mindray shall not be responsible for the effects on safety, reliability, and performance of this product if:
Installation operations, expansions, changes, modifications and repairs of this product are conducted by personnel not authorized by Mindray;
The electrical installation of the relevant room does not comply with the applicable national and local requirements;
The product is not used in accordance with the instructions for use.
III
Warranty Statements Mindray warrants that components within the ultrasound system under warranty will be free from defects in workmanship and materials for the amount of time specified under Mindray’s then-current warranty policy (please check with the Mindray Customer Service Department for the applicable warranty period for each system). Under this warranty, Mindray will repair or replace (at Mindray’s option) any defective component at no charge for materials according to Mindray’s then-current warranty policy. This warranty does not cover consumable items such as, but not limited to, traveling carrying case, acoustic gel, paper, disposable or one-off materials, and sampling materials. Recommended preventative maintenance, as prescribed in the Service Manual, is the responsibility of the user, and is not covered by this warranty. Mindray will not be liable for any incidental, special, or consequential loss, damage, or expense directly or indirectly arising from the use of its products. Liability under this warranty and the buyer’s exclusive remedy under this warranty is limited to servicing or replacing the affected products, at Mindray’s option, at the factory or at an authorized Distributor, for any product which shall under normal use and service appear to Mindray to have been defective in material or workmanship. No agent, employee, or representative of Mindray has any authority to bind Mindray to any affirmation, representation, or warranty concerning its products, and any affirmation, representation, or warranty made by any agent, employee, or representative shall not be enforceable by buyer or user. THIS WARRANTY IS EXPRESSLY IN LIEU OF, AND MINDRAY EXPRESSLY DISCLAIMS, ANY OTHER EXPRESS OR IMPLIED WARRANTIES, INCLUDING ANY IMPLIED WARRANTY OF NON-INFRINGEMENT, MERCHANTABILITY, OR FITNESS FOR A PARTICULAR PURPOSE, AND OF ANY OTHER OBLIGATION ON THE PART OF MINDRAY. Damage to any product or parts through misuse, neglect, accident, or by affixing any non-standard accessory attachments or by any customer modification voids this warranty. Mindray makes no warranty whatever in regard to trade accessories, such being subject to the warranty of their respective manufacturers. A condition of this warranty is that the equipment or any accessories which are claimed to be defective be returned, when authorized, to the appropriate Mindray affiliate. Please contact the Mindray Customer Service Department for appropriate details for your region.
Customer Service Department Manufacturer:
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Address:
Mindray Building, Keji 12th Road South, High-tech industrial park, Nanshan, Shenzhen 518057,P.R.China
Website:
www.mindray.com
E-mail Address:
Tel:
+86 755 81888998
Fax:
+86 755 26582680
IV
Descriptions Committed The following marks are used for describing keys on the control panel, menu items, buttons on dialog boxes and other basic operations in the manual:
.
<Button>: the angle bracket for enclosing the button’s name refers to the buttons on the keyboard, rotation knobs, switches or controls. [Menu item or key]: the square bracket for enclosing menu item or key refers to the menu items or the keys on dialog boxes. Click [Menu item or key]: move the cursor to the menu item or the key on the dialog box, and then press <Set>. Or, click other optional keys on touch screen. [Menu item]-[Sub-menu item]: select sub-menu item based on the operation path
V
1
Safety Precautions
This chapter describes important issues related to safety precautions, as well as the labels and icons on the ultrasound machine.
1.1
Meaning of Signal Words
In this service manual, the signal words DANGER, WARNING, CAUTION and NOTE are used regarding safety and other important instructions. The signal words and their meanings are defined as follows. Please be aware of the meaning of the signal words before reading this manual. Signal word
Description
DANGER
Indicates an imminently hazardous situation that, if not avoided, will result in death or serious injury.
WARNING
Indicates a potentially hazardous situation that, if not avoided, could result in death or serious injury.
CAUTION
Indicates a potentially hazardous situation that, if not avoided, may result in minor or moderate injury.
NOTE
Indicates a potentially hazardous situation that, if not avoided, may result in property damage.
Description
1.2
Important information that helps you to use the system more effectively.
Symbols
The following tables provide location and information of the safety symbols and warning labels, please read carefully.
1.2.1
Meaning of Safety Symbols
Symbol
Position
Description Type-BF applied part
Right side of main unit
Note: The ultrasound probes connected to this system are type-BF applied parts. The ECG module connected to this system is Type-BF applied part. Caution
Main unit
Safety Precautions 1-1
1.2.2 No.
Warning Labels Warning Labels
1.
The following labels are available when the system works with the mobile trolley.
2.
Description
Label Position
Read the manual carefully before using the system.
On the upper left corner of the control panel
a. Do not place the system on a sloped surface. Otherwise the system may slide, resulting in personal injury or the system malfunction. Two persons are required to move the system over a sloped surface.
On the left part of the trolley panel
b. Do not sit on the system. c. DO NOT push the system when the casters are locked.
Non-ionizing radiation 3
1.2.3
On the bottom part of the ultrasound system
General Symbols
This symbols used in the device are listed in the following table. Meanings are: No.
Symbol
Description
1
Type-BF applied part
2
To avoid safety accidents, refer to relevant content in the manual.
3
Dangerous voltage
4
No user serviceable parts (applied to the power adapter)
5
Indoor, dry location use only (applied to the power adapter)
6
Power button
7
Probe sockets
8
USB port
9
S-VIDEO signal port; VIDEO signal port
10
AC (Alternating current)
11
Battery Status Indicator
1-2 Safety Precautions
No.
Symbol
Description
12
Pencil probe port (reserved)
13
IO extend port
14
unlocked symbol
15
locked symbol
16
Battery installation position indicator
17
Connects serial port devices
18
ECG function
19
Connects a display monitor or projector
20
Audio signal
21
Microphone input jack
22
Remote control port
23
Product serial number
24
Manufacture date
25
This product is provided with a CE marking in accordance with the regulations stated in Council Directive 93 / 42 / EEC concerning Medical Devices. The number adjacent to the CE marking (0123) is the number of the EU-notified body certified for meeting the requirements of the Directive.
26
The environment-protective application period of the system is 20 years period.
27
Standby
1.3
Safety Precautions
Please read the following precautions carefully to ensure the safety of the patient and the operator when using the probes.
DANGER:
Do not operate this system in an atmosphere containing flammable or explosive gases such as anesthetic gases, oxygen, and hydrogen or explosive fluid such as ethanol because an explosion may occur.
Safety Precautions 1-3
1.3.1
Electric Safety
WARNING:
1. Connect the power plug of this system and power plugs of the peripherals to wall receptacles that meet the ratings indicated on the rating nameplate. Using a multifunctional receptacle may affect the system grounding performance, and cause the leakage current to exceed safety requirements. Use the power cord accompanied with the system provided by Mindray. 2.
Disconnect the AC power before you clean or uninstall the ultrasound machine, otherwise, electric shock may result.
3. When using peripherals not powered by the auxiliary output of the ultrasound system, or using peripherals other than permitted by Mindray, make sure the overall leakage current of peripherals and the ultrasound system meets the requirement of the local medical device electrical regulation (like enclosure leakage current should be no more than 500uA of IEC 60601-1-1), and the responsibility is held by the user. 4. In maintenance or assembly/disassembly, make sure other cables are connected well before the battery connecting cable is connected, otherwise the system may be damaged due to hot-plug. 5. Do not use this system simultaneously with equipment such as an electrosurgical unit, high-frequency therapy equipment, or a defibrillator, etc.; otherwise electric shock may result. 6. This system is not water-proof. If any water is sprayed on or into the system, electric shock may result.
CAUTION:
1. DO NOT connect or disconnect the system’s power cord or its accessories (e.g., a printer or a recorder) without turning OFF the power first. This may damage the system and its accessories or cause electric shock. 2. Avoid electromagnetic radiation when perform performance test on the ultrasound system. 3. In an electrostatic sensitive environment, don’t touch the device directly. Please wear electrostatic protecting gloves if necessary. 4. You should use the ECG leads provided with the ECG module. Otherwise it may result in electric shock.5. Maximum output power of the trolley is 240 VA.
1-4 Safety Precautions
1.3.2
Mechanical Safety
WARNING:
1. When moving the system, you should first power off the system, fold the LCD display, disconnect the system from other devices (including probes) and disconnect the system from the power supply. 2. Do not subject the transducers to knocks or drops. Use of a defective probe may cause electric shock to the patient.
CAUTION:
1. Do not expose the system to excessive vibration (during the transportation) to avoid device dropping, collision, or mechanical damage. 2. When you place the system on the mobile trolley and move them together, you must secure all objects on the mobile trolley to prevent them from falling. Otherwise you should separate the system from the mobile trolley and move them individually. When you have to move the system with the mobile trolley upward or downward the stairs, you must separate them first and then move them individually. 3. Do not move the ultrasound system if the HDD indicator is green, sudden shake may cause the HDD in damage.4 When moving the trolley with mounted system, please take care of the connector of the power adapter in case of damage.
1.3.3 Note:
Personnel Safety 1. 2. 3.
1.3.4 Note:
The user is not allowed to open the covers and panel of the system, neither device disassemble is allowed. To ensure the system performance and safety, only Mindray engineers or engineers authorized by Mindray can perform maintenance. Only technical professionals from Mindray or engineers authorized by Mindray after training can perform maintenance.
Others For detailed operation and other information about the ultrasound system, please refer to the operator’s manual.
Safety Precautions 1-5
2
Product Specifications
2.1
Introduction
2.1.1
Intended Use
The diagnostic ultrasound system is intended for use in clinical ultrasonic diagnosis.
2.1.2
System Appearance
Product Specifications 2-1
No.
Name
Function
1
Monitor
Displays the images and parameters during the scan.
2
Control Panel
Operator-system interface or control
3
Handle
Used for carrying the system
Power input port
4
Connects the power adapter
5
HDMI port
Outputs high definition multimedia signals
6
USB port
Connects USB devices (2 ports)
7
ECG port
Connects ECG lead or DC-IN cable
8
Probe port
Connects a probe to the main unit; or connects a probe extend module Locks or unlocks the probe connected with the main unit
9
Probe locking lever
:locked symbol :unlocked symbol
10
2.1.2.1
Pencil probe port
Connects to a pencil probe.
Extend Modules
Extend modules to the system are: probe extend module, video/audio extend module.
Probe extend module
No.
Name
Function
<1>
Connector
Connects to the probe port of the main unit, and extends the probe port to three.
<2>
Probe port
To extend ports for connecting probes
2-2 Product Specifications
Note:
1.
Perform the plug and unplug of the probe module. To reduce the wastage of probe module, the operation should be conducted under frozen status of the system.
2.
If you use the probe extend module to connect a probe, the image quality may be degraded.
Audio/Video extend module
Panel introduction
No. <1>
Indicator
Function Used for connecting to main unit. The green indicator is on.
<2>
Used for audio signal output.
<3>
Used for separate video output.
<4>
Symbol
VGA
VGA signal output
Connection
Connect the V/A extend module to the main unit via an HDMI port. As shown in the following figure.
Product Specifications 2-3
2.1.2.2
Control Panel
2-4 Product Specifications