Beneheart d6 Service Manual v80 en

BeneHeart D6
Defibrillator/Monitor
Service Manual

Intellectual Property Statement

SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called
Mindray) owns the intellectual property rights to this product and this manual. This manual
may refer to information protected by copyrights or patents and does not convey any license
under the patent rights of Mindray, nor the rights of others. Mindray does not assume any
liability arising out of any infringements of patents or other rights of third parties.
, , and are the registered trademarks or

trademarks owned by Mindray in China and other countries.
Revision History
This manual has a revision number. This revision number changes whenever the manual is
updated due to software or technical specification change. Contents of this manual are subject
to change without prior notice.
 Version number 7.0
 Release time: May 2011
© 2009-2011 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.
Company Contact
Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
E-mail Address: service@mindray.com
Tel: +86 755 26582479, +86 755 26582888
Fax: +86 755 26582934, +86 755 26582500
I

Preface
Manual Purpose
This manual provides detailed information about the assembling, dissembling, testing and
troubleshooting of the equipment to support effective troubleshooting and repair. It is not
intended to be a comprehensive, in-depth explanation of the product architecture or technical
implementation. Observance of the manual is a prerequisite for proper equipment
maintenance and prevents equipment damage and personnel injury.
Intended Audience
This manual is for biomedical engineers, authorized technicians or service representatives
responsible for troubleshooting, repairing and maintaining the defibrillator/ monitors
Passwords
Passwords may be required to access different modes. The passwords are listed below:
 Installation mode: 888888
 Service mode: 332888
 Configuration mode: 315666
II

Contents
1 Safety................................................................................................................................. 1-1
1.1 Safety Information .......................................................................................................... 1-1
1.1.1 Dangers .............................................................................................................. 1-2
1.1.2 Warnings............................................................................................................. 1-2
1.1.3 Cautions ............................................................................................................. 1-2
1.1.4 Notes .................................................................................................................. 1-3
1.2 Equipment Symbols ........................................................................................................ 1-3
2 Theory of Operation ........................................................................................................ 2-1

2.1 The Basics ....................................................................................................................... 2-1
2.1.1 Overview............................................................................................................ 2-1
2.1.2 Main Functions................................................................................................... 2-1
2.2 Components .................................................................................................................... 2-2
2.3 Main Unit ........................................................................................................................ 2-2
2.4 Front Housing Assembly................................................................................................. 2-4
2.5 Paddle Tray ..................................................................................................................... 2-6
2.6 Rear Housing Assembly.................................................................................................. 2-6
2.6.1 Power System..................................................................................................... 2-6
2.6.2 Main Control System ......................................................................................... 2-7
2.6.3 Therapy System.................................................................................................. 2-7
2.6.4 Parameter Measurement System ........................................................................ 2-7
2.7 External Device Connectors............................................................................................ 2-8
3 Unpacking and Installation ............................................................................................. 3-1

3.1 Unpacking the Equipment............................................................................................... 3-1
3.2 Preparation for Installation.............................................................................................. 3-2
3.2.1 Preparation for Installation Site.......................................................................... 3-2
3.2.2 Electrical Requirements ..................................................................................... 3-3
3.3 Vehicle Mount Kit Installation ........................................................................................ 3-3
3.4 Installing Hook Kit or Conductive Gel Container Kit..................................................... 3-3
3.5 Preparation for Power On................................................................................................ 3-3
3.6 User Test.......................................................................................................................... 3-4
4 Testing and Maintenance................................................................................................. 4-1

4.1 Introduction..................................................................................................................... 4-1
4.1.1 Test Report ......................................................................................................... 4-2
4.1.2 Preventative Maintenance .................................................................................. 4-2
4.1.3 Recommended Frequency.................................................................................. 4-3
4.2 Preventative Maintenance Procedures ............................................................................ 4-4
1

4.2.1 Visual Test .......................................................................................................... 4-4

4.2.2 NIBP Tests.......................................................................................................... 4-4
4.2.3 CO2 Module Tests............................................................................................... 4-7
4.2.4 Preventative maintenance test report.................................................................. 4-8
4.3 Power On Test ................................................................................................................. 4-9
4.4 User Test........................................................................................................................ 4-10
4.5 Password for Installation Mode .....................................................................................4-11
4.6 Module Performance Tests.............................................................................................4-11
4.6.1 Manual Defibrillation Test ................................................................................4-11
4.6.2 Pacing Test ....................................................................................................... 4-13
4.6.3 ECG Test .......................................................................................................... 4-14
4.6.4 Resp Test .......................................................................................................... 4-15
4.6.5 IBP Tests........................................................................................................... 4-15
4.6.6 SpO2 Test.......................................................................................................... 4-17
4.6.7 Temp Test ......................................................................................................... 4-17
4.7 Analogue Output Test.................................................................................................... 4-18
4.8 Electrical Safety Tests ................................................................................................... 4-18
4.9 Recorder Check............................................................................................................. 4-18
4.10 Factory Service ........................................................................................................... 4-18
4.10.1 Password for Service Mode............................................................................ 4-18
4.10.2 Accessing Service Mode Menu ...................................................................... 4-19
4.10.3 Calibrating NIBP............................................................................................ 4-19
4.10.4 Calibrating/Zeroing Impedance...................................................................... 4-19
4.10.5 Device Information ........................................................................................ 4-21
4.10.6 Checking Failure Code................................................................................... 4-21
4.10.7 Inputting Serial Number................................................................................. 4-22
4.10.8 Paddle Open Circuit Display.......................................................................... 4-22
4.10.9 Selecting Recorder Type ................................................................................ 4-22
5 Hardware and Software Upgrade................................................................................... 5-1

5.1 Hardware Upgrade .......................................................................................................... 5-1
5.1.1 Upgrading MPM module ................................................................................... 5-1
5.1.2 MPM Module upgrade procedure ...................................................................... 5-5
5.1.3 Upgrade the Therapy Module............................................................................. 5-7
5.1.4 Upgrade the Equipment with CO2 Module........................................................ 5-8
5.1.5 Upgrade the Recorder ...................................................................................... 5-10
5.2 Software Upgrade through a PC.................................................................................... 5-10
5.2.1 Installing Mindray Patient Monitor Software Upgrade Tool.............................5-11
5.2.2 Software Upgrade Procedure ........................................................................... 5-13
5.3 Software Upgrade through a USB Memory .................................................................. 5-14
5.3.1 Precautions ....................................................................................................... 5-14
5.3.2 Software Upgrade Procedure ........................................................................... 5-14
6 Troubleshooting ................................................................................................................ 6-1
2

6.1 Overview......................................................................................................................... 6-1

6.2 Part Replacement ............................................................................................................ 6-1
6.3 Checking Defibrillator/Monitor Status............................................................................ 6-1
6.4 Checking Device Information......................................................................................... 6-2
6.5 Checking Technical Alarm .............................................................................................. 6-2
6.6 Troubleshooting Guide.................................................................................................... 6-3
6.6.1 Defibrillation Problems...................................................................................... 6-3
6.6.2 Pacing Problems................................................................................................. 6-5
6.6.3 Power On/Off Problems ..................................................................................... 6-5
6.6.4 Display Problems ............................................................................................... 6-6
6.6.5 Alarm Problems.................................................................................................. 6-7
6.6.6 Button and Knob Problems ................................................................................ 6-8
6.6.7 Recorder Problems............................................................................................. 6-9
6.6.8 Output Interface Problems ................................................................................. 6-9
6.6.9 CF Card Problems ............................................................................................ 6-10
6.6.10 Wireless Transmission Module Problems ...................................................... 6-10
6.6.11 Power Supply Problems ..................................................................................6-11
6.6.12 Software Upgrade Problems........................................................................... 6-12
6.7 Technical Alarm Messages............................................................................................ 6-12
6.8 Error Codes ................................................................................................................... 6-13
6.8.1 Therapy Module Error Codes........................................................................... 6-13
6.8.2 Power Module Error Codes.............................................................................. 6-14
6.8.3 Main Control Error Codes................................................................................ 6-15
6.8.4 MPM Error Codes ............................................................................................ 6-15
7 Disassembly and Repair .................................................................................................. 7-1

7.1 Tools Required ................................................................................................................ 7-1
7.2 Preparations for Disassembly.......................................................................................... 7-2
7.3 Disassembling the Main Unit.......................................................................................... 7-3
7.3.1 Removing Hook Mount...................................................................................... 7-3
7.3.2 Removing Paddle Tray....................................................................................... 7-4
7.3.3 Separating the Housing ...................................................................................... 7-5
7.3.4 Removing the Measurement Module Panel ....................................................... 7-6
7.3.5 Removing the Power Supply Assembly ............................................................. 7-8
7.3.6 Discharging the Capacitor.................................................................................. 7-9
7.3.7 Removing the Therapy Module High-voltage Board....................................... 7-10
7.3.8 Disassembling the MPM Module......................................................................7-11
7.3.9 Removing the CO2 Module ............................................................................. 7-12
7.3.10 Removing the CPU board Assembly.............................................................. 7-12
7.3.11 Removing the Therapy Port Assembly........................................................... 7-13
7.3.12 Checking Waterproof Material on the Rear Housing ..................................... 7-14
7.4 Disassembling the Front Housing Assembly................................................................. 7-15
7.4.1 Removing the Keypad board............................................................................ 7-15
7.4.2 Removing Display Assembly ........................................................................... 7-17
3

7.4.3 Removing the Speaker ..................................................................................... 7-20

7.4.4 Removing the Indicating Lamp Board and Alarm Lamp Board ...................... 7-20
7.4.5 Removing the Mode Select Knob .................................................................... 7-21
7.4.6 Removing the Rotary Encoder ......................................................................... 7-22
7.4.7 Removing the Recorder.................................................................................... 7-22
7.5 Disassembling the MPM Module.................................................................................. 7-23
7.5.1 Removing the Fan ............................................................................................ 7-23
7.5.2 Removing the SpO2 board ............................................................................... 7-24
7.5.3 Removing the MPM Module Analog Board .................................................... 7-25
7.5.4 Removing the MPM Module Digital Board..................................................... 7-26
7.5.5 Removing the NIBP Module............................................................................ 7-27
7.6 Disassembling the Power Supply Assembly ................................................................. 7-28
7.6.1 Removing the AC/DC board ............................................................................ 7-28
7.6.2 Removing the Power Supply Sheet Metal and the Grounding Terminal.......... 7-29
7.7 Disassembling the CO2 Module ................................................................................... 7-30
7.7.1 Disassembling the Microstream CO2 Module ................................................. 7-30
7.7.2 Disassembling Mindray CO2 Module.............................................................. 7-31
7.8 Disassembling the Measurement Module Panel Assembly........................................... 7-32
7.8.1 Disassembling the Measurement Module Panel with Mindray CO2 Module.. 7-32
7.8.2 Disassembling the Measurement Module Panel with Microstream CO2 Module
................................................................................................................................... 7-33
7.8.3 Disassembling the Measurement Module Panel without CO2 Module ........... 7-33
7.9 Disassembling the Recorder.......................................................................................... 7-34
7.9.1 Disassembling the TR6F Recorder................................................................... 7-34
7.9.2 Disassembling the TR8A Recorder .................................................................. 7-35
7.10 Disassembling the External Paddle............................................................................. 7-37
7.10.1 Disassembling the Adult Paddle..................................................................... 7-37
7.10.2 Disassembling the Apex Pediatric Paddle...................................................... 7-37
7.10.3 Disassembling the Sternum Pediatric Paddle................................................. 7-38
8 Parts .................................................................................................................................. 8-1

8.1 Introduction..................................................................................................................... 8-1
8.2 Main Unit ........................................................................................................................ 8-2
8.2.1 Exploded View ................................................................................................... 8-2
8.2.2 Parts List ............................................................................................................ 8-2
8.3 Front Housing Assembly................................................................................................. 8-4
8.3.1 Exploded View ................................................................................................... 8-4
8.3.2 Parts List ............................................................................................................ 8-4
8.4 Rear Housing Assembly.................................................................................................. 8-8
8.4.1 Exploded View ................................................................................................... 8-8
8.4.2 Parts List ............................................................................................................ 8-8
8.5 Rear Housing................................................................................................................. 8-10
8.5.1 Exploded View ................................................................................................. 8-10
8.5.2 Parts List ...........................................................................................................8-11
4

8.6 Measurement Module Panel Assembly ......................................................................... 8-12

8.6.1 Exploded View ................................................................................................. 8-12
8.6.2 Parts List .......................................................................................................... 8-12
8.7 Power Supply Assembly ............................................................................................... 8-14
8.7.1 Exploded View ................................................................................................. 8-14
8.7.2 Parts List .......................................................................................................... 8-15
8.8 MPM Module................................................................................................................ 8-16
8.8.1 Exploded View ................................................................................................. 8-16
8.8.2 Parts List .......................................................................................................... 8-17
8.9 Capacitor Assembly ...................................................................................................... 8-18
8.9.1 Exploded View ................................................................................................. 8-18
8.9.2 Parts List .......................................................................................................... 8-18
8.10 Sidestream CO2 Module Kit ....................................................................................... 8-19
8.10.1 Exploded View ............................................................................................... 8-19
8.10.2 Parts List ........................................................................................................ 8-19
8.11 Microstream CO2 Module Kit .................................................................................... 8-20
8.11.1 Exploded View ............................................................................................... 8-20
8.11.2 Parts List......................................................................................................... 8-20
8.12 Paddle Tray Assembly................................................................................................. 8-21
8.12.1 Exploded View ............................................................................................... 8-21
8.12.2 Parts List ........................................................................................................ 8-21
8.13 External Paddle ........................................................................................................... 8-22
8.13.1 Exploded View ............................................................................................... 8-22
8.13.2 Parts List ........................................................................................................ 8-22
8.14 Sternum Pediatric Paddle Kit ...................................................................................... 8-23
8.14.1 Exploded View ............................................................................................... 8-23
8.14.2 Parts List ........................................................................................................ 8-23
8.15 Sternum Adult Paddle Kit ........................................................................................... 8-24
8.15.1 Exploded View ............................................................................................... 8-24
8.15.2 Parts List ........................................................................................................ 8-24
8.16 Apex Pediatric Paddle Kit ........................................................................................... 8-25
8.16.1 Exploded View ............................................................................................... 8-25
8.16.2 Parts List ........................................................................................................ 8-25
8.17 Apex Adult Paddle Kit ................................................................................................ 8-26
8.17.1 Exploded View ............................................................................................... 8-26
8.17.2 Parts List ........................................................................................................ 8-26
8.18 External Paddle Cable ................................................................................................. 8-27
8.18.1 Exploded View ............................................................................................... 8-27
8.18.2 Parts List ........................................................................................................ 8-27
8.19 Hook Mount ................................................................................................................ 8-28
8.19.1 Exploded View ............................................................................................... 8-28
8.19.2 Parts List ........................................................................................................ 8-28
8.20 Replacement Parts....................................................................................................... 8-29
8.20.1 Main Unit ....................................................................................................... 8-29
5

8.20.2 Connecting Cables ......................................................................................... 8-32
6

1 Safety
1.1 Safety Informatio n
DANGER
 Indicates an imminent hazard that, if not avoided, will result in death, serious
personal injury or property damage.
WARNING
 Indicates a potential hazard or unsafe maintenance practice that, if not avoided,
could result in death, serious personal injury, product / property damage.
CAUTION
 Indicates a potential hazard or unsafe maintenance practice that, if not avoided,
could result in minor personal injury or product/property damage
NOTE
 Provides application tips or other useful information to ensure that you can better
service your product.
1-1

1.1.1 Dangers
WARNING
 Do not open the equipment cases to avoid shock hazard. All servicing and future
upgrades must be carried out by the personnel trained and authorized by our
company only.
1.1.2 Warnings
WARNING
 To avoid high voltage shock, disconnect the defibrillator/monitor from AC adapter
and remove the batteries before disassembly.
 The equipment must be connected to a properly installed power socket with

protective earth contacts only. If the installation does not provide a protective
earth conductor, do not use this socket and operate the equipment on rechargeable
batteries.
 When disposing of the packaging material, be sure to observe the applicable waste
control regulations and keep it out of children’s reach.
1.1.3 Cautions
CAUTION
 Make sure that no electromagnetic radiation interferes with the performance of the
equipment when preparing to carry out performance tests. Mobile phone, X-ray
equipment or MRI devices are a possible source of interference as they may emit
higher levels of electromagnetic radiation.
 Before connecting the equipment to the power line, check that the voltage and
frequency ratings of the power line are the same as those indicated on the
equipment’s label or in this manual.
 Protect the equipment from damage caused by drop, impact, strong vibration or
other mechanical force during servicing.
1-2

1.1.4 Notes
NOTE
 Refer to Operation Manual for detailed operation and other information.
1.2 Equip ment Symbols
Attention: Please read this

manual carefully before Equipotential terminal
servicing.
Danger: High-voltage Service indicator
Alternating current(AC) Network connector
Battery Video output
USB connector Analog input/out
ESD warning symbol for Electrostatic sensitive devices.
Type CF applied part. Defibrillator-proof protection against electric shock.
Type BF applied part. Defibrillator-proof protection against electric shock.
1-3

FOR YOUR NOTES
1-4

2 Theory of Operation
2.1 The Basics
2.1.1 Overview
BeneHeart D6 defibrillator/monitor (hereinafter called the equipment) provides four
operating modes: Manual Defib, AED, Pacer, and Monitor. The equipment is for use in
hospital and pre-hospital settings. It adopts the most advanced biphasic defibrillation
technology and can deliver up to 360J of defibrillation energy.
BeneHeart D6 has an 8.4" LCD display.
2.1.2 Main Functions

The equipment has the following main functions:
 Manual Defib Mode
In Manual Defib Mode, the operator analyzes the patient’s ECG, and, if appropriate, follows
this procedure:
1 Select the Manual Defib mode, adjust the energy level if necessary
2 Charge; and
3 Deliver the shock.
Defibrillation may be performed through external paddles or multifunction electrode pads. In

Manual Defib Mode, you can also perform synchronized cardioversion.
 AED Mode
In AED mode, the equipment automatically analyzes the patient’s ECG rhythm and
indicates whether or not a shockable rhythm is detected. Voice prompts provide
easy-to-follow instructions and patient information to guide you through the
defibrillation process. Messages and flashing buttons are also presented to reinforce the
voice prompts.
 Pacer Mode
The Pacer Mode offers non-invasive transcutaneous pacing therapy. Pace pulses are
delivered through multifunction electrode pads using a monophasic square waveform.
2-1

 Monitor Mode
In Monitor Mode, the equipment is intended for monitoring, displaying, reviewing,

storing and printing multiple physiological parameters and waveforms including ECG,
pulse oximetry (SpO2), temperature (Temp), non-invasive blood pressure (NIBP),
invasive blood pressure (IBP) and carbon dioxide (CO2).
2.2 Components
The equipment consists of a main unit, accessories and PC software.
The main unit is the core of the equipment. It provides:
 Overall system control;
 System power supply;
 Display;
 Defibrillation and pacing;
 AED ;
 Man-mahcine interface;
 Audible and visible alarms;
 Multiple parameter measurements;
 External connectors and communication; and
 Recording, printing and data storage.
2.3 Main Unit
The main unit is composed of the front housing assembly, rear housing assembly and the
paddle tray assembly. External paddles are rested in the paddle tray.
 The front housing assembly mainly consists of LCD, keypad board, recorder, speaker,
microphone, Mode Select knob, navigation knob, backlight inverter, alarm lamp board,
indicating lamp board, front housing and front housing sheet metal, etc.
 The rear housing assembly consists of CPU board, therapy module, high voltage
capacitors, MPM module, CO2 module, power management board, wireless network
adapter, fan, measurement module panel, therapy port, and rear housing, etc.
 The paddle tray is for holding the external paddles.
2-2

The main unit consists of the following subsystem:
 Input subsystem: Its input includes keypad board, microphone, Mode Select knob,
navigation knob, and paddle handle controls.
 Output subsystem: includes display screen, alarm lamp board, recorder, and speaker
 Processing and communication subsystem: includes CPU board, therapy module, MPM
module, and CO2 module.
 Power management subsystem: includes batteries, AC/DC board and power

management board.
 External device connection subsystem: includes USB connector, network connector,

VGA connector and multifunction connector for analog output and synchronous input.
System Structure
2-3

System Signal Flow
2.4 Front Housing Assembly

The front housing assembly consists of display assembly (including the backlight inverter), a
keypad board, a recorder, a speaker, a microphone, a Mode Select knob, a navigation knob,
an alarm lamp board, an indicating lamp board, a front housing and front housing sheet metal,
etc.
Navigation Knob
You can rotate the knob clockwise or counterclockwise and then press it to confirm a
selection. The knob is connected to the keypad board.
Mode Select Knob

A 8-position encoder is used to select the operating mode (Monitor, Manual Defib, AED and
Pacer) and power-off. The unused positions are mechanically disabled.
Recorder
The recorder receives data from the CPU board and then sends the data to a thermal head for
printing. The recorder front panel has a key for starting/ stopping the recorder and a green
indicator which is lit when working normally. The recorder is connected to the keypad board
which board provides connection for the TR6F recorder. The block diagram and functional
modules of the recorder are shown as below.
2-4

Module Description
Power Interface Introduces DC power supply from the CPU board.

Recorder Power Module Adjusts input voltage to run each module.
Coordinates module communication, controls and processes module
Recorder CPU
status.
Serves as the data communication channel between the keypad board
Keypad board Interface
and the recorder CPU.
Receives control signals sent by the recorder CPU to drive the step
Motor Drive Circuit
motor.
Keypad and Indicator Sends keypad commands to CPU and receives CPU commands to
Interface control the indicator.
Sends print head information to CPU and receives CPU commands to
FPC Interface
control the print head.
Speaker
The speaker emits alarm tones, key-stroke tone, heart beats and PR sound. It supports the
functions of PITCH TONE and the multi-level volume. The speaker is connected to the
keypad board.
Microphone
It provides the function of voice recording.
Al arm Lamp B oar d

The keypad board interfaces with the alarm lamp board. The alarm lamp transmits signals to
drive the green and yellow alarm lamp.
Indicating Lamp Board

The keypad board interfaces with the indicating lamp board. On the equipment’s front panel,
there are 3 indicators: AC power indicator, battery indicator and service indicator, each has an
icon aside.
2-5

2.5 Paddle Tray

The paddle tray is used to hold paddles. It has a 50 Ω test load inside. When the equipment
runs self tests, test current will pass through the test load.
2.6 Rear Housin g Assembly

Rear housing assembly consists of the CPU board, the therapy module, high voltage
capacitors, a MPM module, a CO 2 module, a power management board, a fan, a rear housing,
a measurement module panel, and a therapy port, etc.
2.6.1 Power System
The power system consists of the following items:
 AC/DC board: The AC mains is the input, and the outputs is 18VDC.
 Battery: 14.8V, 4500mAh.
 Power Management Board
It is intended for power transform and battery charge control. The system outputs four
types of power supply: 18V (when AC mains is used) or 14.8V (when a battery is used),
12V, 5V, and 3.3V.
The priority of system power supply is rated in the order of AC mains, Battery 1 and
Battery 2. That is to say, when AC is not available, Battery 1 will be used; if Battery 1 is
defective or depleted, Battery 2 will be used.
2-6

2.6.2 Main Con tr ol System

The CPU board is connected with the power management board with stacking connectors, as
shown below.
The main control module mainly consists of the CPU and FPGA. CPU is used to provide
least required internal storage, program memory, large capacity non-volatile storage, and the
watch dog. It connects EEPROM and other peripheral ICs such as Ethernet PHY chip. FPGA
performs the main functions of display and audio. Besides, it has the function of adapting
interfaces from CPU to MPM module, the keypad board and the recorder. CPU controls
FPGA via Flexbus.
2.6.3 Therapy System

The therapy system provides the functions of defibrillation, pacing and AED analysis. The
therapy module is an unseparated assembly.
The therapy module adopts DSP+MCU framework. MCU is responsible for therapy control
while DSP for ECG and impedance detection, AED algorithm, monitoring algorithm, pacing
algorithm, auxiliary therapy control, etc.
2.6.4 Parameter Measurement System

MPM modules and the CO2 module are used to provide parameter monitoring. However,
ECG monitoring can also be implemented by the therapy module. .
2-7

2.7 External Device Connectors
6
7
2
3 9
4 5
1. Hook
2. Battery 2
3. Battery 1
4. External power input: It connects an AC power cord or a DC/AC adapter to run the
equipment respectively on the external AC mains or DC power supply.
5. Equipotential grounding terminal: When the defibrillator/monitor and other devices are
to be used together, their equipotential grounding terminals should be connected
together to eliminate the potential difference between them.
6. USB connector: It connects the USB memory for data export. Data stored in the internal
CF card can be transferred to the USB memory and then export to a PC via the data
management software.
7. Network connector: It is a standard RJ45 connector, through which software can be

upgraded.
8. Multifunctional connector: provides ECG analog output and defibrillation

synchronization input.
9. VGA connector: connects an external VGA display.
2-8

3 Unpacking and Installation

This chapter provides information you need to install a defibrillator/monitor ready for use.
3.1 Unpackin g t he Equipment

Open the package and take out the packing list. Check that all the articles included in the
packing list are available and the quantity and specification are correct.
 All the optional parts purchased by the customer shall also be checked.
 Notify the supplier if provided components are not correct as compared to the packing
list.
 In case of damage during transportation, keep the packing material and notify the
supplier immediately.
 Keep the packing material till new equipment is accepted.
The following pictures show the defibrillator/monitor and accessory packing.
Accessory packing Main unit
Main unit packing
Accessory packing
3-1

3.2 Preparation for Installation
3.2.1 Preparation for Installation Site
1. Ensure that the site meets all safety, environmental and power requirements
2. Check that required power sockets are available.
3. Check that a network connector is available if the defibrillator/monitor needs to be

connected to network.
WARNING
 Only power cables provided with the system may be used. For reasons of safety,
power (mains) extension cables or adapters shall not be used.
Environmental Requirements
WARNING
 To avoid explosion hazard, do not use the equipment in the presence of flammable
anaesthetics, vapours or liquids.
CAUTION
 The environment where the defibrillator/monitor will be used should be reasonably

free from vibration, dust and corrosive substances. If these conditions are not met,
the accuracy of the system may be affected and damage may occur.
The environmental specification is as follows:
0 to 45℃ (without CO2 module)

Operating Temperature 5 to 35℃ (with sidestream CO2 module)
0 to 40ºC (with microstream CO2 module)
Operating humidity 15% to 95%, (non-condensing)
Operating altitude -381m to +4575 m (-1250 ft to 15000 ft, or 106.2kPa to 57kPa)
Storage temperature -30 to 70℃
Storage humidity 10% to 95%, (non-condensing)
Storage altitude -381m to +4575 m (-1250 ft to 15000 ft, or 106.2kPa to 57kPa)
3-2

3.2.2 Electrical Requirements

Check cables and power cords. Make sure that:
1. All system cables, power cords and power plugs are not damaged, and pins are not loose.
Otherwise, remove it from use.
2. The insulation of patient cables and leadwires is not damaged, and connectors are not
loose.
WARNING
 Only power sockets with protective grounding can be used.
The electrical specification is as follows:

Line voltage: 100 to 240VAC
Current: 1.8 to 0.8 A
Frequency: 50/60Hz
3.3 Vehicle Mount Kit Installation

Refer to BeneHeart D6/D5 Vehicle Mount Kit Instructions for Use for the detailed
information on how to install the equipment on the vehicle mount kit.
3.4 Installing Hook Kit o r Conductive Gel Container Kit

Refer to Hook Kit and Conductive Gel Container Kit Installation Guide to install the hook
kit or conductive gel container kit.
3.5 Preparation fo r Power On

Before connecting the power cord to the defibrillator/monitor's power input, check that
 The mains voltage meets the requirement.
 3-wire power cord is used. The power socket should be 3-wire also. This ensures that the
defibrillator/monitor is properly grounded. Do not use 2-wire power cord or socket.
 The equipotential grounding terminals should be connected together when the

defibrillator/monitor and other devices are to be used together.
 The defibrillator/monitor is not placed under the infusion bag or placed where their
might be liquid spillage. This protects the defibrillator/monitor from liquid ingress.
3-3

3.6 User Test

A user test shall be performed after the defibrillator/monitor is installed. Follow this
procedure:
1. Connect AC mains or install the battery.
2. Connect the external paddles. If pads are used, connect the test load.
3. Select the Main Menu button on the equipment’s front panel and select [User Test >>].
Select all test items and press [ Start] to perform user test.
NOTE
 Install the battery and properly place the external paddles in the paddle tray or
connect the pads cable and 50 Ω test load. Otherwise the User Test will fail.
Refer to BeneHeart D6 Operating Manual for the detailed information on user test.
3-4

4 Testing and Maintenance

4.1 Introductio n
To ensure the equipment always functions normally, qualified service personnel should
perform regular inspection, maintenance and test. This chapter provides a checklist of the
testing procedures for the equipment with recommended test equipment and frequency. The
service personnel should perform the testing and maintenance procedures as required and use
appropriate test equipment.
The testing procedures provided in this chapter are intended to verify that the equipment
meets the performance specifications. If the equipment or a module fails to perform as
specified in any test, repairs or replacement must be done to correct the problem. If the
problem persists, contact our Customer Service Department.
CAUTION
 All tests should be performed by qualified service personnel only.
 Care should be taken to change the settings in [Installation Mode] and [Service
Mode] menus to avoid loss of data.
 Before testing, service personnel should acquaint themselves with the test tools and
make sure that test tools and cables are applicable.
 When testing monitoring parameters, move the Mode Select knob to Monitor to
access the Monitor Mode.
 When performing therapy function tests, move the Mode Select knob to
corresponding mode.
4-1

4.1.1 Test Report

After completing the tests, service personnel are required to record test results and report
them to Mindray Customer Service Department.
See the
Test Report at the end of this chapter.
4.1.2 Preventative Maint enance

Below are preventative maintenance tests which need to be performed on the
defibrillator/monitor. See the following sections for detailed maintenance procedures.
 Visual inspection
 NIBP test and calibration
 Microsteam and Sidestram CO2 test and calibration.
4-2

4.1.3 Recommended Frequenc y

After Function 6 12 24
Test item
repair suspected months months months
Visual inspection ×
Power-on Test ×
User test ×
Recorder check ×
Charge/
Manual discharge
defibrillation Energy disarming
× × ×
tests Synchronous
defibrillation
Pacing test
Performance test × × ×
ECG
Module calibration × ×
Resp Performance test × × ×
SpO2 Performance test × × ×
Temp Performance test × × ×
Accuracy test
NIBP Leakage test × × ×
Module calibration
Performance test
IBP
Pressure calibration
Leakage test × × ×
CO2
Module calibration × × ×
NIBP overpressure protection test × × ×
Analog out test ×
Earth leakage current

Electrical
safety tests as Patient leakage
× ×
per current
IEC60601-1 Patient auxiliary
current
4-3

4.2 Preventative Maintenance Procedur es
4.2.1 Visual Test

Inspect the equipment for obvious signs of damage. The test is passed if the equipment has no
obvious signs of damage. Follow these guidelines when inspecting the equipment:
 Carefully inspect the housing, the display screen and the buttons for physical damage.
 Inspect accessories for signs of damage.
 Inspect all external connections for loose connectors, bent pins or frayed cables.
 Inspect all connectors on the equipment for loose connectors or bent pins.
 Make sure that safety labels and data plates on the equipment are clearly legible.
4.2.2 NIBP Test s

Ac cu rac y Test
Tools required:
 T-shape connector
 Tubing
 Balloon pump
 Metal Vessel, volume 500±25 ml
 Calibrated manometer for reference, accuracy not lower than 1 mmHg
To perform the accuracy test:
1. Connect the equipment as shown below.
Defibrillator/monitor
Manometer
Connector for Tubing
NIBP cuff
Balloon pump Metal vessel
2. Before inflation, the reading of the manometer should be 0. If not, disconnect the airway
and reconnect it until the readings is 0.
3. Press the Main menu button on the equipment’s front panel. Select
[Others>> ]→[Installation Mode>>]→ enter the required password→[Maintain
NIBP]→ [Start Accuracy Test].
4-4

4. Compare the value of manometer with the value displayed on the equipment’s screen.
The difference should be no greater than 3 mmHg.
5. Raise the pressure in the metal vessel to 50 mmHg with the balloon pump. Repeat steps
3 and 4.
6. Raise the pressure in the metal vessel to 200 mmHg with the balloon pump. Repeat steps
3 and 4.
Note
 You can replace the balloon pump and manometer with a blood pressure simulator
to form a test system.
NIBP Leakage Test

Tools required:
 An adult cuff
 An air tubing
 A correct sized cylinder
To perform the leakage test:
1. Connect the cuff to the equipment’s NIBP connector.
2. Wrap the cuff around the cylinder as shown below.
Cylinder
Defibrillator/monitor
Connector for
Tubing
NIBP cuf Cuff
3. Press the Main menu button on the equipment’s front panel. Select [Others>> ]→
[Installation Mode>>]→ enter the required password →[Maintain NIBP]→ [Start
Leakage Test].
After about 20 seconds, the equipment automatically deflates. This means the leakage test
finishes.
When the accuracy test is completed, the result will be displayed. If the message [NIBP
Pneumatic Leak ] is displayed, it indicates that the NIBP airway may have leakages. Check
the tubing and connections for leakages, and then perform a leakage test again.
4-5

Calib rating NIBP

Tools required:
 Tubing
 Balloon pump
 Metal Vessel, volume 500±25 ml
 Calibrated manometer, accuracy higher than 1 mmHg
1. Connect the equipment as shown below
Defibrillator/monitor Manometer
Connector for Tubing

NIBP cuff
Balloon pump
Metal vessel
2. Before inflation, the reading of the manometer should be 0. If not, disconnect the
airway and reconnect it until the readings is 0
[Service Mode>>]→ enter the required password→[Calibrate NIBP].
4. Calibrate pressure. To do so, set the calibration value to 150 mmHg and adjust the pump
output pressure to 150 mmHg. After the system is stable, click the [Calibrate] button to
start calibration.
5. Calibrate overpressure. To do so,
 set [Patient Cat.] to [Adu/Ped] and adjust pump output pressure to 330 mmHg.
Click the [Calibrate] button and start calibration. Or
 set [Patient Cat.] to [Neo] and adjust pump output pressure to 165 mmHg. Click
the [Calibrate] button and start calibration.
All the calibration results will be displayed in the [Calibrating NIBP] screen. If the
calibration fails, please check the connections and then perform a calibration again.
4-6

4.2.3 CO2 Module Tests

Leakage Check
1. Access the [CO2 Setup] menu and set [Operating Mode] to [Measure]. Wait for CO2
warm-up.
2. Block the CO2 module gas inlet completely. This will cause different reactions from the
Sidestream and Microstream CO2 modules.
 Sidestream: Check that alarm message [ CO2 Filter Line Err] is displayed on the
screen in 3s. Block the gas inlet for another 30s, if the alarm message does not
disappear, the module does not leak.
 Microstream CO2 module: [CO2 Purging…] is displayed in 3s. Block the gas inlet

for another 30s, if the alarm message [ CO2 Tubing Err] appears, the module does
not leak.
Module Calibration
Test tools
 Gas cylinder, with 6% of CO 2 and balance gas N 2.
 Tubing
For sidestream CO2 module, zeroing is required before calibration. Enter [ CO2 Setup] menu
and select [Zero] to perform zeroing.
To calibrate the CO2 module, follow this procedure:
1. Make sure that the CO2 module has been warmed up or started up.
2. Connect the gas cylinder with the tubing using a T-shape connector as shown below.
Check the airway and make sure there are no leaks.
To the air
Tubing
Gas valve
Defibrillator
/monitor
Gas cylinder
4-7

3. Vent the tubing to the CO2 by opening the gas valve.
4. Access the [Maintain CO2] menu. To do so, Press the Main Menu button on the
equipment’s front panel. Select [Others>> ]→[Installation Mode>>] →enter the
required password→ [Maintain CO2].
5. In the [Maintain CO2] menu, select a CO2 value equal to the vented CO2
concentration.
6. In the [Calibrate CO2] menu, the measured CO2 concentration is displayed. Wait till
the measured CO2 concentration becomes stable; select [Calibrate] to start CO2
calibrate.
The message [Calibration Completed!] is displayed after a successful calibration. If the

calibration failed, the prompt [Calibration Failed!] will be displayed. In this case, perform
another calibration.
4.2.4 Preventativ e maintenance t est r eport

Customer name
Customer address
Servicing person
Servicing company
Equipment under test

(EUT)
Model of EUT
SN of EUT
Hardware version
Software version
Test equipment Model/No. Effective date of calibration
4-8

Test items Test records Test results

(Pass/Failed)
Visual inspection
The case, display screen, buttons, knob, SMR, modules, power

cord, wall-mount bracket and accessories have no obvious signs
of damage.
The external connecting cables are not frayed and the connector
pins are not loose and bent.
The external connectors are not loose or their pins are not bent.
The safety labels and data plate are clearly legible.
NIBP test
The difference is within ±3 mm when 0, 50 or 200 mmHg is set

for NIBP accuracy test.
There is no leakage with NIBP, or the manual leakage test result

does not exceed 6mmHg/min.
Sidestream CO2 test
Block the gas inlet of the module or watertrap. The sidestream

CO2 flowrate is slower than 10ml/min and an alarm of CO2
Filterline Err is given. It indicates that there is no leakage.
The displayed CO2 value is within 6 ±0.05％.
Microstream CO2 test
Block the gas inlet of the module or watertrap. An alarm of CO2

4.3 Power On Test

This test is to verify that the defibrillator/ monitor can power on normally. The test is passed if the
defibrillator/ monitor starts up by following this procedure:
1. Place the external paddles on paddle tray, insert the battery (install both if two batteries
are configured) in the battery compartment, and then connect the equipment with AC
mains. In this case, both the AC indicator and battery indicator shall light.
2. Turn the Mode Select knob to Monitor. Check that the equipment passes the self test and
is turned on properly.
3. Check the display of technical alarm area, prompt area and battery status indicator on
the upper right corner of the main screen to judge whether the equipment runs normally.
4-9

4.4 User Test

Follow this procedure to perform user test:
1. If you use external paddles, place them on the paddle tray; if you use a pads cable,
connect it to the 50 Ω test load.
2. Insert the battery (2 if configured) into the equipment. Connect the AC mains if no
battery is available.
3. Select the Main Menu button on the equipment’s front panel. In the Main Menu, select
[User Test>>]. Then a prompt “Enter user test?” pops up. Select “Yes” to enter the User
Test screen.
4. Check the test items you want to perform and select [Start] to start user test
The test results indicate the condition of the system. If any item fails, the service indicator
flashes.
If you cannot pass User Test or the message “Connect paddles cable, and place paddles in
paddle tray” is shown when paddle cable is connected and paddles are placed in paddle tray,
check paddles status.
Select the Monitor mode. Press and hold the [ Event] hardkey, and then press the [ Lead
Select ] hardkey on the front panel, the following screen appears.
Observe the reading of “Lead Stat”:
 0 x 382: Paddles are properly placed in paddle tray.
 0 x 182: The travel switch indicating paddle status may fail, but impedance is correct.
 0 x 102 :Paddles are not properly placed in paddle tray and the impedance value is not
correct.
4-10

4.5 Password for Installation Mode

Accessing installation mode is password protected. The required password is set to 888888
before the equipment leaves the factory.
4.6 Module Performance Tests
4.6.1 Manual Defibrill ation Test

Test tools:
 Defibrillator/pacer analyzer
Charge/Discharge
1. Remove the batteries and connect the equipment with AC mains. Turn the Mode Select
knob to Manual Defib.
2. Connect the external paddles to the equipment and place the paddles on the
defibrillator/pacer analyzer.
3. Enter the Configuration-Main screen. From the Record Setup menu set [Shock Event]
to [On] so that shock events can be recorded automatically if happened.
4. Set the analyzer to Energy Measurement mode. In this case, the energy value should be
displayed as 0 or blank.
5. Select the energy level to 1J.
6. Charge/discharge the equipment to verify the energies measured by the analyzer meet
the following accuracy:
Selected Energy (J) Measured Value (J)

1 0 to 3
100 85 to 115
360 306 to 414
7． Set the energy to 100J and 360J respectively. Repeat Step 6.
8. Disconnect the equipment from the AC mains. Run the equipment on fully charged
battery. Move the Mode Select knob to Manual Defib. Repeat Steps 5 to 7.
9. Use multifunctional electrode pads. Repeat Step 5 to Step 7.
10. Verify that the equipment records the shock events automatically and correctly.
4-11

Energy Disarming
1. Run the equipment on fully charged battery. Move the Mode Select knob to Manual
Defib.
2. Connect the external paddles to the equipment and place the paddles on the
5. Charge the equipment.
6. Verify that the charge tone is issued during charging.
7. Press the “Disarm” soft key to discharge the energy internally.
8. Verify that a prompt “Charge Removed” appears and the charge done tone stops.
9. Verify that the value measured by the analyzer is 0J or blank.
10. Enter the Configuration-Main menu, select [Manual Therapy Setup] and set [Time to
Auto Disarm] to [60s].
11. Exit “Configuration Management”. The equipment restarts automatically.
14. Charge the equipment. Count time after charging is completed.. Verify that the prompt
“Shock Removed” appears on the equipment and the energy measured by the analyzer is
0J or blank after 60 seconds.
15. Use multifunctional electrode pads. Repeat Step 3 to Step 14.
Synchronous Defibri llation

1. Connect the external paddles and ECG cable to the equipment. Place the paddles ECG
electrodes on the defibrillator/pacer analyzer.
2. Set the analyzer to Measurement Mode and output normal sinus rhythms, e.g. amplitude
value 1mV and HR 60bpm.
3. Enter Configuration Management. In the [Manual Therapy Setup] menu, set [Sync
After Shock ] to [On].
4. Adjust the energy setting of the equipment to be 10J.
5. Press the [Sync On] soft key to start synchronous defibrillation. If Remote Sync is
switched on, press the [ Sync On] soft key and select [ Local] to start synchronous
defibrillation
6. Select [Pads] or [Paddles] as the ECG source and begin charging.
4-12

7. When charging finishes, press and hold the “Shock” button to deliver a shock.
8. Verify that synchronous discharge succeeds and the delivery energy measured by the
analyzer is 10J±2J.
9. Verify that the delay time of synchronous defibrillation measured by the analyzer is less
than 60ms.
10. Verify that the synchronous discharge mark appears on the R wave.
11. Verify that the prompt messages are correct during testing.
12. Select lead II as ECG source and perform charging. Repeat steps 7 to 11.
13. Use multifunctional electrode pads. Repeat steps 2 to 12.
4.6.2 Pacing Test

Test tools:
 Defibrillator/pacer analyzer
1. Run the equipment on fully charged battery. Move the Mode Select knob to Pacer. Set
[Pacer Mode] to [Fixed].
2. Connect the pads cable to the equipment and properly place the pads on the
3. Set the analyzer to Pacing Measurement mode. Use test load of 50 Ω.
4. On the equipment, set [Pacer rate] to [70ppm] and [Pacer Output] to [30mA].
5. Press the [Start Pacing] soft key. Verify that the pacer rate measured by the analyzer is
70 ppm±1ppm and the pacer output measured is 30 mA±5mA.
6. Press the “Stop Pacing” soft key, and then set [ Pacer rate] to [170ppm] and [Pacer
Output] to [200mA].
7. Press the [Start Pacing] soft key. Verify that the pacer rate measured by the analyzer is
170 ppm±2ppm, and the measured current is 200 mA±10mA.
4-13

4.6.3 ECG Test

Perfo rmance Test
Test tools
 ECG simulator
1. Connect the simulator to the equipment’s ECG connector.
2. Configure the simulator as HR=80 bmp.
3. The displayed HR should not exceed 80±1 bmp;
ECG Calib ration
1. Select the ECG parameter area to enter the [ ECG Setup] menu.
2. Select [Others>> ]→[Calibrate]. A waveform signals appear on the screen and the
message [ECG Calibrating] is displayed in the prompt information area in the lower
left corner of the screen.
3. Compare the amplitude of the waveform with the wave scale. The difference should be
within 5%. If needed, you can also print out the waveform and the wave scale.
4. After ECG calibration is completed, select [Stop Calibrating].
4-14

4.6.4 Resp Test

Test tools
 Resp Patient simulator
1. Connect the patient simulator to the Resp connector on the module.
2. On the defibrillator/monitor, select the Resp widow to enter the Resp Setup menu. Set
[Lead] to [II].
3. Configure the simulator as follows: set Lead to II, base impedance line to 1500 Ω; delta
impedance to 0.5 Ω, and respiration rate to 40 rpm.
4. Check that respiration waveform is not distorted and the displayed Resp value does not
exceed 40±2 rpm.
4.6.5 IBP Tests

Perfo rmance Test
Test tools
 Patient simulator
1. Connect the patient simulator to any of the equipment’s IBP connector.
2. Set the pressure value of patient simulator to 0.
3. Zero the transducer. To do so, vent the transducer to atmospheric pressure by turning on
the stopcock to the air. Select an IBP parameter window, e.g. Art, to enter [ Art Setup]
menu. Select [Art Zero>>]→[Zero] to start a zero calibration. After the completion of
zero calibration, close the stopcock to the air and open the stopcock to the patient.
4. Set the static pressure of the simulator to P=200 mmHg.
5. The displayed value should not exceed 200±2 mmHg.
6. If the difference exceeds ±2 mmHg, calibrate IBP.
4-15

Pressure Calibration
Tools required:
 Standard sphygmomanometer
 Balloon pump
 Tubing
To perform a calibration:
1. Connect the 3-way stopcock, the sphygmomanometer and the balloon pump through a
T-shape connector, as shown below.
2. Zero the transducer. Then open the stopcock to the sphygmomanometer.
[Installation Mode>>]→ enter the required password→[Maintain IBP]. Then
configure IBP calibration value.
4. Inflate using the balloon pump until the reading of sphygmomanometer approximates
the preset calibration value.
Pressure transducer
3-way stopcock
Pressure adapter cable

T-shape connector
IBP Module
Sphygmomanometer
5. Adjust the calibration value in the [Maintain IBP] menu until it is equal to the reading
of sphygmomanometer
6. Select the [Calibrate] button to start a calibration
7. The message [Calibration Completed!] is displayed after a successful calibration. If

the calibration failed, the prompt [Calibration Failed!] will be displayed.
4-16

4.6.6 SpO2 Test
Test tool
 Patient simulator.
1. Connect the patient simulator to the equipment’s SpO2 connector .
2. Select the model and manufacturer of the SpO2 module under test. Configure the
parameter as SpO2 96% and PR 80 bmp.
3. The displayed SpO2 and PR values should be within the ranges listed below
SpO2 (%) PR (bmp)
Mindray 96% ±2% 80±3

Masimo 96% ±2% 80±3
MAX-A, MAX-AL, MAX-N, MAX-P, MAX-I,

96% ±2%
MAX-FAST
Nellcor OxiCliq A, OxiCliq N, OxiCliq P, OxiCliq I 96% ±2.5% 80±3

D-YS, DS-100A, OXI-A/N, OXI-P/I 96% ±3%
MAX-R, D-YSE, D-YSPD 96% ±3.5%
4.6.7 Temp Test

Test tools
 Resistance box
1. Connect the two pins of any Temp connector on equipment to the two ends of the
resistance box using 2 wires.
2. Set the resistance box to 1354.9Ω (corresponding temperature is 37℃). The displayed

value on the equipment should not exceed 37±0.2℃.
4-17

4.7 Analogue Output Test

Test tool:
 Oscillograph
1. Connect the patient simulator to the equipment under test using an ECG or IBP cable.
2. Connect the oscillograph to the equipment’s multifunctional connector.
3. Verify that the waveforms displayed on the oscillograph is identical with those
displayed on the defibrillator/ monitor.
4.8 Electr ical Safety Tests

See A Electrical Safety Inspection for electrical safety tests..
4.9 Recorder Check

Tools required:
 None.
1. Print ECG waveforms. The recorder should print correctly and the printout should be
clear.
2. Simulate some recorder problems, such as out of paper, paper jam, etc. the defibrillator/
monitor should give corresponding prompt messages. After the problem is removed, the
recorder should be able to work correctly.
3. Switch automatic alarm recording for each parameter ON and then set each parameter’s
limit outside set alarm limits. Corresponding alarm recordings should be triggered when
parameter alarms occur.
4.10 Factory Service
4.10.1 Passwor d for Servi ce Mode

Accessing service mode is password protected. The required password is set to 332888
before the equipment leaves the factory.
4-18

4.10.2 Accessing Service Mode Menu

To access the factory service menu, Press the Main menu button on the equipment’s front
panel. Select [Others>> ]→ [Service Mode>>]→ enter the required passwords. The Service
Mode-Main menu is shown below.
4.10.3 Calibrating NIBP

Refer to 4.2.2 NIBP Tests for calibrating NIBP.
4.10.4 Calib rating/Zeroing Impedance

Normally impedance calibration and zeroing is unnecessary. However, you can perform
impedance checking after replacing the therapy module.
1. If not pre-connected, connect the pads cable to the equipment.
2. Connect a test load of 300 ohms to the pads cable.
3. Start the equipment and select the Monitor mode. Press and hold the [Event] hardkey,
and then press the [ Lead Select] hardkey on the front panel, the following screen
appears.
4-19

4. Verify that the reading of “RT Imped” is between 3000±450.
NOTE
 If 300 ohms test load is not available, you can use a 50 ohms test load to perform
impedance checking. In this case, Verify that the reading of “RT Imped” is
between 500±75.
If the reading of “RT Imped” is not correct, perform impedance calibration/zeroing.
[Service Mode>>]→ enter the required passwords→[Calibrate/Zero Impedance] to
enter the Calibrate/Zero Impedance screen.
2. Connect a test load of 0 ohm to the pads cable; then select “Zero”. A message “Zero
Completed” shall be shown. If the message “Zero Failed” is displayed, check the
connection of pads cable.
3. Connect a test load of 100 ohms to the pads cable; then select “Calibrate”. A message
“Calibration Completed” shall be shown. If the message “Calibration Failed” is
displayed, check the connection of pads cable.
Replace the therapy module if impedance calibration/zeroing fails.
4-20

4.10.5 Device Infor matio n

Press the Main menu button on the equipment’s front panel. Select [ Others>> ]→ [Service
Mode>>]→ enter the required passwords→ [Device Information]. In the Device
Information list, you can view the device information such as software version, system status,
and etc, as shown below.
In the Device Information screen, you can select [ Export] to export error codes and shock
delivery data to a USB flash memory.
4.10.6 Checking Failu re Code

Press the Main Menu button on the equipment’s front panel. Select [ Others>> ]→ [Service
Mode>>]→ enter the required passwords→ [Failure Code] to check error codes. This helps
the service personnel to identify failures.
Refer to 6.8 Error Codes for the description of each error code.
4-21

4.10.7 Inputt ing Serial Numb er

Press the Main Menu button on the equipment’s front panel. Select [ Others>> ]→ [Service
Mode>>]→ enter the required passwords→ [Input Serial Number] to input the equipment’s
serial number.
After inputting the serial number, you can view it by accessing Installation Mode and select
[Version].
4.10.8 Paddle Open Circ uit Display

This [Paddle Open Circuit Display] switch is for testing only. In normal operation, it should
be set to [Off ]].
4.10.9 Selectin g Recor der Typ e

BeneHeart D6 defibrillator/monitor can be configured with a 50 mm recorder or an 80 mm
recorder. You can choose the recorder type in the service mode by selecting [ Recorder Type]
and toggle between [50 mm Recorder] and [80 mm Recorder].
4-22

Test Repor t
Customer name
Customer address
Servicing person
Servicing company
Equipment under test

(EUT)
Model of EUT
SN of EUT
Hardware version
Software version
Test equipment Model/No. Effective date of calibration
4-23

Test results
Test items Test records
(Pass/Failed)
Visual inspection
The case, display screen, buttons, knob, modules, power cord, and
accessories have no obvious signs of damage.
The external connecting cables are not frayed and the connector pins
are not loose and bent.
The external connectors are not loose or their pins are not bent.
The safety labels and data plate are clearly legible.
Power-on test
The power-on test is passed. The power indicator and alarm system
work correctly and the equipment start up properly.
Performance test
Manual Defibrillation Test
When running on AC mains and external paddles are used, the

equipment can be properly charged and discharged; the energy
delivered meets accuracy requirement, and shock information is
correctly recorded.
When running on fully charged battery and external paddles are used,
the equipment can be properly charged and discharged; the energy
delivered meets accuracy requirement, and shock information is
correctly recorded.
When running on AC mains and multifuncational electrode pads are

used, the equipment can be properly charged and discharged; the
energy delivered meets accuracy requirement, and shock information
is correctly recorded.
When running on fully charged battery and multifuncational

electrode pads are used, the equipment can be properly charged and
discharged; the energy delivered meets accuracy requirement, and
shock information is correctly recorded.
When external paddles are used, charge tone is correctly issued when
the equipment is being charged. The prompt "Charged Removed" is
shown on the screen and charge done tone stops when the Disarm
hotkey is pressed. The equipment does not discharge externally.
When [Time to Auto Disarm] is set to [60s], the prompt "Charged
Removed" is shown on the screen and the charge done tone stops
after 60 seconds at the completion of charging. The equipment does
not discharge externally.
When pads are used, the charge tone is correctly issued when the
equipment is being charged. The prompt "Charged Removed" is
4-24

Test results
(Pass/Failed)
shown on the screen and the charge done tone stops when the Disarm
hotkey is pressed. The equipment does not discharge externally.
When [Time to Auto Disarm] is set to [60s], the prompt "Charged
Removed" is shown on the screen and the charge done tone stops
after 60 seconds at the completion of charging. The equipment does
not discharge externally.
When external paddles are used for synchronous defibrillation and

ECG source is paddles and lead II respectively, the prompt is correct
and a Sync mark appears above each R wave. The delivered energy
measured is 10J±2J and the synchronous shock is delivered within 60
ms of the peak of the R-wave.
When pads are used for synchronous defibrillation and ECG source
is paddles and lead II respectively, the prompt is correct and a Sync
mark appears above each R wave. The delivered energy measured is
10J±2J and the synchronous shock is delivered within 60 ms of the
peak of the R-wave.
Pacing Test
When set [Pacer rate] to [70ppm] and [Pacer Output] to [30mA],

the pacer rate measured by the analyzer is 70 ppm±1ppm and the
pacer output measured is 30 mA±5mA.
When set [Pacer rate] to [170ppm] and [Pacer Output] to

[200mA], the pacer rate measured by the analyzer is 170 ppm±2ppm,
and the measured current is 200 mA±10mA.
ECG performance test
ECG waves are displayed correctly without noise and the HR value
is within 80±1 bpm.
ECG Lead Off alarm behaves correctly.
Paced signals are detected and pace pulse marks are displayed when
[Paced] is set to [Yes]
The difference between the amplitude of the ECG calibration square

wave and that of the wave scale is not greater than 5%.
Resp test
Resp wave is not distorted and the Resp value is within 40±2 rpm.
NIBP test
The difference is within ±3 mm when 0, 50 or 200 mmHg is set for

NIBP accuracy test.
There is no leakage with NIBP, or the manual leakage test result does
4-25

Test results
(Pass/Failed)
not exceed 6mmHg/min.
Temp test
The value displayed for each Temp channel of the monitor is within
37±0.1ºC.
IBP test
The static pressure value displayed for each IBP channel is within
200±2 mmHg.
The ART and LV waves for each IBP channel are displayed correctly.
Sidestream CO2 test
Block the gas inlet of the module or watertrap. The sidestream CO2
flowrate is slower than 10ml/min and an alarm of CO2 Filterline Err
is given. It indicates that there is no leakage.
Miscrostream CO2 test
Block the gas inlet of the module or watertrap. An alarm of CO2

The displayed CO2 value is within 6 ±0.05％
Analog output performance test
The waves displayed on the oscillograph are identical with those

displayed on the monitor.
SpO2 test
The displayed SpO2 and PR values should be within the specified

ranges.
Electrical safety tests
Refer to Appendix A Electrical Safety Inspection. All the electrical

safety tests should be passed.
Recorder check
The recorder can print ECG waves correctly and the printout is clear.
Set the recorder to some problems such as out of paper, paper jam,
etc. the equipment gives corresponding prompt messages. After the
problem is removed, the recorder is able to work correctly.
Automatic alarm recording for each parameter functions correctly
when parameter alarms occur.
Tested by: _________________________ Date: ________________________
4-26

5 Hardware and Software Upgrade

5.1 Hardware Upgr ade
After upgrade the hardware, please upgrade corresponding software.
5.1.1 Upgrading MPM module

Upgrading MPM modul e confi gured w ith 3/5-lead ECG onl y
You can upgrade MPM module from 3/5-lead ECG only to any of the following
configuration:
PN Description of upgrade package Configuration after upgrade
801-0651-00117-00 Low cost MPM subassembly 12-Lead 12-lead ECG

ECG upgrade package
801-0651-00118-00 12-Lead ECG/Mindray SpO2upgrade 12-lead ECG/Mindray SpO2

package
801-0651-00049-00 NIBP upgrade package 3/5-lead ECG/NIBP
801-0651-00050-00 Mindray SpO2 upgrade package 3/5-lead ECG/Mindray SpO2
801-0651-00051-00 Masimo SpO2 upgrade package 3/5-lead ECG/Masimo SpO2
801-0651-00052-00 Nellcor SpO2 upgrade package 3/5-lead ECG/Nellcor SpO2
801-0651-00053-00 Mindray SpO2/NIBP/TEMP upgrade 3/5-lead ECG/Mindray SpO2

package /NIBP/TEMP
801-0651-00056-00 Mindray SpO2/NIBP/IBP/TEMP 3/5-lead ECG/Mindray SpO2

upgrade package /NIBP/IBP/TEMP
801-0651-00059-00 Masimo SpO2/NIBP/TEMP upgrade 3/5-lead ECG/Masimo SpO2

package /NIBP/TEMP
801-0651-00060-00 NellcorSpO2/NIBP/TEMP upgrade 3/5-lead ECG /Nellcor SpO2

package /NIBP/TEMP
801-0651-00061-00 Masimo SpO2/NIBP/IBP/TEMP upgrade 3/5-lead ECG/Masimo SpO2

package /NIBP/IBP/TEMP
801-0651-00062-00 NellcorSpO2/NIBP/IBP/TEM upgrade 3/5-lead ECG/Nellcor SpO2

5-1

Upgrading MPM modu le co nfi gured w ith 3/5-leadECG/NIBP

You can upgrade MPM module from 3/5-lead ECG/NIBP to any of the following
configuration:
801-0651-00053-00 Mindray SpO2/NIBP/TEMP upgrade 3/5-lead ECG/Mindray SpO2

package /NIBP/TEMP
801-0651-00056-00 Mindray SpO2/NIBP/IBP/TEMP upgrade 3/5-lead ECG/Mindray SpO2

801-0651-00059-00 Masimo SpO2/NIBP/TEMP upgrade 3/5-lead ECG/Masimo SpO2

package /NIBP/TEMP
801-0651-00061-00 Masimo SpO2/NIBP/IBP/TEMP upgrade 3/5-lead ECG/Masimo

package SpO2/NIBP/IBP/TEMP
801-0651-00060-00 NellcorSpO2/NIBP/TEMP upgrade 3/5-lead ECG/Nellcor

package SpO2/NIBP/TEMP
801-0651-00062-00 NellcorSpO2/NIBP/IBP/TEMP upgrade 3/5-lead ECG/Nellcor

801-0651-00116-00 12-lead ECG upgrade package 12-lead ECG
Upgrading MPM modu le con fig ured wi th 3/5-lead ECG/Mind ray SpO2
You can upgrade MPM module from 3/5-lead ECG/Mindray SpO2 to any of the following
configuration:
801-0651-00118-00 12-lead ECG/Mindray SpO2upgrade 12-lead ECG

package
801-0651-00053-00 Mindray SpO2/NIBP/TEMP upgrade 3/5-lead ECG/Mindray

801-0651-00056-00 Mindray SpO2/NIBP/IBP/TEMP upgrade 3/5-lead ECG/Mindray

5-2

Upgrading MPM modu le con fig ured w ith 3/5-lead ECG/Masim o SpO2
You can upgrade MPM module from 3/5-lead ECG/Masimo SpO2 to any of the following
configuration:
801-0651-00059-00 Masimo SpO2/NIBP/TEMP upgrade 3/5-lead ECG/Masimo

801-0651-00061-00 Masimo SpO2/NIBP/IBP/TEMP upgrade 3/5-lead ECG/Masimo

Upgrading MPM modu le con fig ured wi th3/5-lead ECG/Nellcor SpO2

You can upgrade MPM module from 3/5-lead ECG/Nellcor SpO2 to any of the following
configuration:
801-0651-00060-00 NellcorSpO2/NIBP/TEMP 3/5-lead ECG/Nellcor

upgrade package SpO2/NIBP/TEMP
801-0651-00062-00 NellcorSpO2/NIBP/IBP/TEMP 3/5-lead ECG/Nellcor

upgrade package SpO2/NIBP/IBP/TEMP
Upgrading MPM modul e confi gured w ith 3/5-lead ECG/Mindray

SpO2/NIBP/TEMP
You can upgrade MPM module from 3/5-lead ECG/Mindray SpO2/NIBP/TEM to any of the
following configuration:
801-0651-00081-00 IBP upgrade package 3/5-lead ECG/Mindray

SpO2/NIBP/IBP/TEMP
5-3

Upgrading MPM modul e confi gured w ith 3/5-lead ECG/Mindray

SpO2/NIBP/TEMP
You can upgrade MPM module from 3/5-lead ECG/Mindray SpO2/NIBP/TEM to any of the
801-0651-00081-00 IBP upgrade package 3/5-lead ECG/Mindray

SpO2/NIBP/IBP/TEMP
Upgrading MPM modul e confi gur ed with 3/5-lead ECG/ Nellcor

SpO2/NIBP/TEMP
You can upgrade MPM module from 3/5-lead ECG/ Nellcor SpO2/NIBP/TEMP to any of the
PN Description of upgrade Configuration after upgrade

package
801-0651-00081-00 IBP upgrade package 3/5-lead ECG/Nellcor

SpO2/NIBP/IBP/TEMP
Upgrading MPM modul e confi gur ed with 3/5-lead ECG/ Mindray

SpO2/NIBP/IBP/TEMP
You can upgrade MPM module from 3/5-lead ECG/ Mindray SpO2/NIBP/IBP/TEMP to any
of the following configuration:
PN Description of upgrade package Configuration after

upgrade
5-4

Upgrading MPM modul e confi gur ed with 3/5-lead ECG/ Masimo

SpO2/NIBP/IBP/TEMP
You can upgrade MPM module from 3/5-lead ECG/ Masimo SpO2/NIBP/IBP/TEMP to any
Upgrading MPM modul e confi gur ed with 3/5-lead ECG/Nellc or

SpO2/NIBP/IBP/TEMP
You can upgrade MPM module from 3/5-lead ECG/ Nellcor SpO2/NIBP/IBP/TEMP to any
5.1.2 MPM Modul e upgr ade proc edure
1. Remove the MPM module assembly and parameter panel assembly as described in 7.3.8
Disassembling the MPM Module.
2. Replace the old parameter panel assembly and MPM module assembly with those in the
upgrade package.
3. Remove the watertrap receptacle unit, or microstream CO2 connector assembly, or CO2
panel as described in 7.8 Disassembling the Measurement Module Panel Assembly.
4. Reassemble the watertrap receptacle unit, or microstream CO2 connector assembly, or

CO2 panel on the replacement parameter panel assembly in the upgrade package.
NOTE
 If you need to upgrade 3/5-lead ECG to 12-lead ECG, insert the 12-lead ECG
board into the MPM module. Make sure that the 12-lead ECG board should be in
correct direction. Then fix the clip in place.
5-5

Cli 2 Clip 1
12-lead ECG board Clip here in place Clip here in place
5. Reassemble the equipment.
6. Stick correct parameter panel overlay on the parameter panel according to the
configuration you upgrade.
 If the upgrade MPM module is equipped with Masimo SpO2, you need to stick a
Masimo label on the lower left corner of the front housing and a No Implied
License label below the parameter panel, as indicated in the following pictures.
Masimo label
No Implied License label
 If the upgraded MPM module is equipped with Nellcor SpO 2, you need to stick a
Nellcor label at the lower left corner of the front housing, as indicated in the
following pictures.
Nellcor label
7. Perform the tests as described in 4.6 Module Performance Tests.
5-6

5.1.3 Upgrade the Therapy Modul e

You can use 801-0652-00039-00 pacer function upgrade kit to upgrade the therapy module so
that equipment has pacing function. After upgrading the therapy module, choose Mode label
(with pacing function) with the language you need.
Follow this procedure to upgrade the therapy module:
1. Remove therapy module as described in 7.3.7 Removing the Therapy Module

High-voltage Board . Be noted that you need not to remove the parameter panel
assembly and MPM module assembly.
2. Take off the Mode Select knob. Peel off the Mode label.
3. Replace the old therapy module with the one configured with pacing function in the
upgrade package.
4. Replace the old Mode Select knob and Mode label with those in the upgrade package.
5. Reassemble the equipment.
Mode Select knob
Mode label
6. After upgrade the therapy module, perform the tests described in 4.6 Module
Performance Tests.
5-7

5.1.4 Upgr ade the Equipment wi th CO2 Modul e

You can use the following CO2 upgrade package to upgrade the equipment so as to have a
CO2 monitoring function.
PN Description of upgrade package
801-0651-00079-00 M02B CO2 upgrade package (for adult/pediatric) (FRU)

801-0651-00082-00 M02B CO2 upgrade package (for neonate) (FRU)
801-0651-00080-00 Microstream CO2 upgrade package (for neonate) (FRU)
Follow this procedure to upgrade the equipment:
1. Remove the parameter module panel assembly as described in 7.3.4 Removing the
Measurement Module Panel .
2. Remove the left capacitor sheet metal as described in 7.3.9 Removing the CO2 Module.
3. Install the required M02B CO2 module or microstream CO2 module on the left
capacitor sheet metal.
Mindray CO2 module Microstream CO2 module
Make sure that the part number of

connecting cable for the microstream
CO2 connector fixing plate should
be 0651-20-77166.
4. Apply the CO2 insulating sheet on the MPM module mounting plate. Be careful to align
the edge of insulating plate with the edge of the metal plate when stick the insulating
plate to the metal sheet. Do not stick the screw holes on the metal sheet. Then bent the
insulating plate properly to avoid being cut by the insulating plate during later assembly
process.
5-8

CO2
insulating plate
Align the edge of

insulating plate with the
edge of the metal plate
Bent here
5. Peel off the overlay on the parameter module panel and install the connector fixing part
of the microstream CO2 module or the watertrap receptacle kit and the gas outlet of the
Mindray CO2 module on the parameter module panel. Choose an appropriate overlay
from the upgrade package and apply it on the parameter module panel.
Gas outlet
Mindray CO2 Microstream CO2

watertrap kit connector fixing part
6. Install the left capacitor metal sheet with CO2 module in the machine.
7. Reassemble the machine. Route the gas pipes to avoid blocking them.
8. Perform the tests as described in 4.2.3 CO2 Module Tests.
5-9

5.1.5 Upgrade the Record er

You can use the TR8A recorder upgrade package (FRU) (801-0651-00133-00) to upgrade the
recorder from TR6F to TR8A.
Follow this procedure to upgrade the recorder:
1. Remove the TR6F recorder as described in .7.9 Disassembling the Recorder.
2. Respectively plug the TR8A connecting cable into the recorder module’s J1 and J3
sockets. Use two M3×6 Philips screws to secure the recorder.
Recorder TR8A recorder

connecting cable
3. Perform the test as described in 4.9 Recorder Check.
5.2 Software Upgrade through a PC

You can upgrade system software and module software using Mindray Patient Monitor
Software Upgrade Tool. You can also view software upgrade log. Mindray Patient Monitor
Software Upgrade Tool can directly run on a PC. By connecting the defibrillator/monitor to a
PC via a crossover network cable, you can upgrade the following software:
 Bootstrap
 System software
Language library
 BMP files (including screen icons, start-up screens, standby screens)
 General configurations (including passwords, company logo)
 System functional configuration
 FPGA program
 Power module software
 MPM, Mindray CO2 module, and therapy module software
5-10

5.2.1 Installing Mindray Patient Monitor Software Upgrade Tool
1. Find the installation program and double click it to start

installation.
2. Select installation language.
3. Click [Ok ] and the following screen appears. Click [ Next] to go to the next step.
4. Enter User Name, Company Name and Serial Number.
5. Specify the destination folder for installing this program. Then select [Next].
5-11

6. Select Program Folder. Then select [ Next].
7. Click [Finish] to complete installation.
5-12

5.2.2 Software Upgrade Proc edure
1. Connect the defibrillator/monitor to be upgraded with a PC.
2. Set IP address to 77.77.XX.XX and subnet mask to 255.255.255.0.
3. Run Mindray Patient Monitor Software Upgrade Tool on the PC and set Machine to
BneneHeart.
4. On the Mindray Patient Monitor Software Upgrade Tool screen, select [ Select Package]
and select packages you want to upgrade. Then select [ Start].
5. Simultaneously hold the [Summary] key and [Menu] key on the defibrillator/monitor’s
front panel, and then turn on the equipment.
After software upgrade is finished, turn off the equipment, and then disconnect AC mains and
remove the battery. If you do not disconnect the power supply after software upgrade, the
status indicator will flash and the beeper will sound.
For the details of software upgrade, refer to help and instructions for use of Mindray Patient
Monitor Software Upgrade Tool.
CAUTION
 Disconnect the equipment from the patient and make sure the important data are
saved before upgrade.
 Do not shut down or power off the equipment when upgrading the boot program.
Otherwise, it may cause the equipment to break down.
 Program upgrade should be performed by qualified service personnel only.
 Crossover network cable shall be used if a PC is connected for equipment upgrade.
NOTE
 After upgrading the boot program, re-upgrade the system program and other
programs to ensure compatibility.
 Make sure the version of the upgrade package is the one that you desired. If you
want to obtain the latest upgrade package, contact Mindray Customer Service
Department.
5-13

5.3 Software Upgrade thr ough a USB Memory

You can upgrade the defibrillator/monitor’s system software and module software using a
USB memory. All software that can be upgraded through a PC can be upgraded through a
USB memory.
5.3.1 Precautions
1. Software upgrade through USB memory is only applied to defibrillator/monitors with

BIOS version 2.0 or later.
2. If you are going to upgrade the software through a PC, do not plug a USB memory to
the defibrillator/monitor’s USB connector.
3. Up to 15 upgrade files can be placed to the “UPGRADE_0651” folder. If more files are
placed, only the first 15 can be displayed and chosen.
4. Only one upgrade file can be chosen at a time. Repeat steps 3 to 5 as described in 5.3.2
Software Upgrade Procedure to upgrade files one by one.
5. The name of files in directory “UPGRADE_0651” should be in English. Otherwise the

file name will be unreadable.
6. Both .pkg and .mpkg files can be upgraded. Bootstrap cannot be included in the .mpkg
files.
7. The bootstrap of main control should be upgrade separately. That is to say, it cannot be
included in the upgrade package.
5.3.2 Software Upgrade Proc edure
1. Create a folder named “UPGRADE_0651” in the root directory of the USB memory.
2. Copy the file “updatecontrol.bin” and upgrade files to directory “UPGRADE_0651”.
3. Turn off the defibrillator/monitor. Plug the USB memory to the equipment’s USB
connector.
4. Simultaneously hold the [Summary] key and [Menu] key on the defibrillator/monitor’s
front panel, and then turn on the equipment.
5. Follow the on-screen instructions to upgrade the software. Choose a file to be upgraded
by rotating the navigation knob. Press down the navigation knob to confirm the selection.
You have to choose the upgrade file within 120 s. If not, software upgrade fails. The
system will upgrade automatically when the upgrade file is selected and confirmed.
5-14

6 Troubleshooting
6.1 Overv iew
In this chapter, the defibrillator/monitor problems are listed along with possible causes and
recommended corrective actions. Refer to the tables to check the defibrillator/monitor,
identify and eliminate the problems.
The problems we list here are frequently arisen difficulties and the actions we recommend
can correct most problems, but not all of them. For more information on troubleshooting,
contact our Customer Service Department.
6.2 Part Replacement

Printed circuit boards (PCBs), major parts and components in the defibrillator/monitor are
replaceable. Once you isolate a defective PCB, follow the instructions in 7 Disassembly and
Repair to replace the PCB with a known good one and check that the trouble disappears or
the defibrillator/monitor passes all performance tests. If the trouble remains, replace the PCB
with the original suspicious PCB and continue troubleshooting as directed in this chapter.
To obtain information on replacement parts or order them, refer to 8 Parts.
6.3 Checking Defibrill ator/Monitor Status

Some troubleshooting tasks may require you to identify the hardware version and status of
your defibrillator/ monitor. To check equipment status,
1. Select [Main Menu] →[Review >>]→[Event Review >>]. Then you can view the
information on system start time, self check, etc.
2. You can also view the information on the defibrillator/monitor’s current status by
pressing the Menu key on the equipment’s front panel, and then selecting
[Others>> ]→[Service Mode>>]→ enter the required password →[Device
Information>>].
6-1

6.4 Checking Device Information

Some troubleshooting may involve software compatibility. Thus it requires you to know your
defibrillator/monitor configuration and software version. For detailed information on version
compatibility, please contact our Customer Service Department.
To identify your software version, press the Menu key on the equipment’s front panel, and
then select [Others>> ]→[Installation Mode>>]→enter the required password →[Version].
In the Version screen, you can view system software version and module software version.
You can also press the Menu key on the equipment’s front panel, and then select
[Others>> ]→[Service Mode>>]→ enter the required password →[Device Information>>]
to check system software version, module software version, and device status .
6.5 Checking Technical Alarm

Before troubleshooting the defibrillator/monitor, check for technical alarm message. If an
alarm message is presented, eliminate the technical alarm first. For detailed information on
technical alarm message, possible cause and corrective action, refer to the
defibrillator/monitor’s Operation Manual.
6-2

6.6 Troubleshoo ting Guide
6.6.1 Defib rill ation Problems

Symptom Possible Cause Corrective Action
Keypad board failure Connect external paddles. Press the

“Charge” button on the Apex paddle to
start charging. If the “Charge” button
The equipment
on the paddles works, it indicates the
does not charge
keypad board fails.
by pressing the
2. Replace the keypad board.
Charge button on
The Charge button fails to be Disassemble the keypad board to
the front panel.
pressed down effectively due to replace or reshuffle the keypad.
the damaged or dislocated silica
gel keypad.
Paddles not connected properly. Reconnect the paddles.
The equipment Paddles failure. Press the Charge button on the front
cannot be charged panel to check if the equipment can be
by pressing the charged. If yes, the paddles fail.
Charge button on Replace the paddles.
the external Therapy module failure Replace the therapy module.
paddles.
Failure of connection wire to the Replace the connection wire
therapy module.
Charging failed Therapy module failure 1. Restart the equipment to check if the
problem disappears.
2. Replace the therapy module if the
problem persists.
Battery failure. Replace the battery or connect the
The equipment is equipment with external power supply.
charged too
Power management board failure. Replace the power management board.
slowly
Therapy module failure Replace the therapy module.
A shock cannot be Keypad board failure. Connect paddles to charge the

delivered by equipment and deliver a shock. If a
pressing the shock can be delivered, the keypad
Shock button on board is defective. Replace the keypad
the equipment’s board.
front panel in The Charge Button fails to be Disassemble the keypad board. Replace
Manual Defib pressed down effectively due to or reshuffle the keypad
Mode or AED the failure or dislocated silica gel
Mode. keypad.
6-3

Paddles not connected properly. Reconnect the paddles.

Paddles failure. Connect pads cable and test load to
A shock cannot be
charge the equipment and deliver a
delivered by
shock. If a shock can be delivered, the
pressing the
paddles fail. Replace the paddles.
Shock button on
the paddles.
Connection wire to the therapy Replace the connection wire.
module broken
The message. Therapy module failure Replace the therapy module.
“Disarming
Failed” is
displayed.
The equipment Too high or too low patient
can be charged, impedance detected. Ensure good connection between the
but the energy is 1. Pads/paddles are detached from patient and pads/paddles. If the problem
disarmed the patient. persists, replace paddles, pads, or pads
automatically at 2. Pads/paddles failure. cable.
the completion of 3. Pads cable failure.
charging or when Therapy module failure Replace the therapy module.
the equipment is
being discharged.
Defibrillation Defibrillation hardware circuit Replace the therapy module.
malfunction. defective.
Keypad board failure 1. Connect paddles and perform energy
setting.
2. Check if energy level can be
Energy Select
selected. If yes, the keypad board is
buttons on the
defective. Replace the keypad board.
equipment front
The Energy Select Buttons fail to Disassemble the keypad board. Replace
panel do not work.
be pressed down due to the or reshuffle the keypad.
damaged or dislocated silica gel
keypad.
Paddles not connected properly. Reconnect the paddles
Energy Select
Paddles failure. Replace the paddles.
buttons on the
paddles do not
Connection wires to the therapy Replace the connection wires.
work
module broken
The message Configuration files not properly Upgrade the configuration files.
“Defibrillation upgraded.
malfunction” Therapy module failure Replace the therapy module.
presented at
power-on
6-4

6.6.2 Pacin g Prob lems

Does not deliver Therapy module failure Replace the therapy module.
correct pacing
current.
Does not deliver Therapy module failure Replace the therapy module.
correct pacing
rate.
Pacer Equip Pacer hardware failure Replace the therapy module.

Malfunction
6.6.3 Power On/Off Problems

The AC mains not connected or Check that AC mains is properly connected

defibrillator/monitor battery too low or battery capacity is sufficient
fails to start. AC Power supply protection Refer to 6.6.11 Power Supply Problems.
LED or battery LED
Cables defective or poorly 1. Check that the cables between the power
does not light
connected switch and the keypad board, the keypad
board and the power management board
and between the power module and the
power management board are correctly
connected.
2. Check that wires and connectors are not
defective.
Power switch or keypad Replace the power switch or keypad board.
board failure
AC/DC board defective Replace the AC/DC board.
Power management board Replace the power management board.
failure
6-5

6.6.4 Displ ay Problems

The LCD screen is Connection cable 1. Check that wires between the display and
blank, but the defective or poorly the keypad board, the backlight board and
defibrillator/monitor connected. the keypad board, the backlight board and
works properly. the display and between the keypad board
and the power management board are
correctly connected.
2. Check that the cables and connectors are
not defective
Backlight inverter Replace the backlight board.
defective
LCD Display failure Replace the display.
Keypad board failure Replace the keypad board.

CPU board failure. Replace the CPU board.
failure.
Secondary display Cable failure 1. Check that the wires between the display
does not function. and the defibrillator/monitor are correctly
connected.
not defective.

failure.
Secondary display Connection cable 1. Check that the wires between the display
displays snows or defective or poorly and the defibrillator/ monitor are correctly
flashing specks connected. connected.
not defective.
failure.
Images overlapped or FPGA failure Update or upgrade FPGA

distorted Connection cable 1. Check that the wire between the display
defective or poorly and keypad board is correctly connected.
connected. 2. Check that the cables and connectors are
not defective.
6-6

The colour of images Connection cable 1. Check that wires between the display and
deviates from the defective or poorly the keypad board, the backlight board and
standard connected. the keypad board, the backlight board and
configuration. the display and between the keypad board
and the power management board are
correctly connected.
not defective.
Display failure Replace the display.
failure.
6.6.5 Alarm Problems

The alarm Connection cable defective or 1. Check that wire between alarm LED board
lamp is not poorly connected. and keypad board are properly connected.
light or 2. Check that connection wires and
extinguished connectors are not defective.
but alarm
Alarm LED board failure Replace the alarm LED board.
sound is issued
Power management board
Replace the power management board.
failure.
No alarm Audio alarm disabled Check that alarm tone volume is set to a value
sound is issued other than zero by pressing the Menu key on
but alarm lamp the equipment’s front panel, and then
is lit selecting [Alarm Setup >>].
Connection cable defective or 1. Check that the wire between the speaker
poorly connected. and keypad board is properly connected.
2. Check that connection wires and
connectors are not defective.
FPGA audio logic ERROR Upgrade the audio logic part of the FPGA
program.
Speaker failure Replace the speaker..

Power management board
Replace the power management board.
failure.
6-7

6.6.6 Butto n and Kn ob Prob lems

Buttons do not Connection cable 1. .Check that the wire between the keypad and the
respond. defective or poorly keypad board is properly connected.
connected. 2. Check that that the wire between the keypad
board and the power management board is properly
connected
3. Check if the connection wires and connectors are
defective.
Keypad board Replace the keypad board.
failure
Power management Replace the power management board.
board failure.
Mode Select knob Connection cable 1. Check that wires between the knob to keypad
does not respond. defective or poorly board, and between the keypad board and the power
connected. management board are properly connected
2. Check that connecting wires and connectors are
not defective.
Knob failure Replace Mode Select knob.

failure
board failure.
Navigation knob Connection cable 1. Check that wires between the knob to keypad
does not respond. defective or poorly board, and between the keypad board and the power
connected. management board are properly connected
2. Check that connection wires and connectors are
not defective.
Knob failure. Replace the navigation knob.

failure

board failure.
6-8

6.6.7 Recor der Prob lems

No printout Connection cable 1. Check the wire between the recorder and the
defective or poorly keypad board is connected properly.
connected. 2. Check that connection wires and connectors are not
defective.
Recorder power Check if the power module outputs 5 V DC and 12V

supply failure DC correctly
Recorder failure Replace the recorder
Poor print quality Paper roll not Stop the recorder and re-install the paper roll.
or paper not properly installed
feeding properly Print head dirty 1. Check the thermal print head and the paper roller
for foreign matter.
2. lean the thermal print head with an appropriate
clean solution
Recorder failure Replace recorder
Blank printout Paper-roll installed Reload paper-roll

reversely.
Recorder failure Replace the recorder
6.6.8 Output Interface Problems

No analog output signals The wires of analog Replace the cable.
output ports defective..
Power management Replace the power management

board failure. board.
USB Device does not function CPU board failure. Replace the CPU board.
(provided that the peripheral Power management Replace the power management
devices are good) board failure. board.
6-9

6.6.9 CF Card Problems

CF card malfunctions Wrong CF card or Use only INNODISK-manufactured CF

limited memory space storage cards. Those with minimum 1GB
memory space are recommended.
CF card defective Insert a known good CF card into the
defibrillator/monitor. If it works normally,
the original CF card fails.
CF card slot failure Replace the CPU board.
CF card failure Format the CF card.
6.6.10 Wireless Transmissi on Module Probl ems

Faxing failure SIM card is not installed. Check that SIM card is installed.
“Data and fax” service is not Verify that “data and fax” service is
activated. activated.
Y cable and wireless Check that Y cable and wireless
transmission module are not transmission module are connected with the
connected with the unit. unit properly.
Antenna is loose. Tighten the antenna.
Fax machine failure Check that the fax machine works properly.
Wireless transmission Replace the wireless transmission module.
module failure
Y cable failure Replace the Y cable.

failure
6-10

6.6.11 Power Supply Prob lems

Battery failure Battery damaged. Replace battery.
Battery interface failure. 1. Check batteries are installed properly.
2. Check if the battery interface is defective.
3. If the battery interface is defective,
replace the power management board.
board failure.
Batteries can not be Battery damaged. Replace batteries.
fully charged. Battery interface failure. 1. Check batteries are installed properly.
2. Check if the battery interface is defective.
3. If the battery interface is defective, replace
the power management board.
board failure.
Battery cannot be Battery failure. Replace battery and recharge the replacement
charged battery. If the replacement battery can be
recharged, the original one fails.
Cable defective or Check batteries are installed properly.
poorly connected 2. Check if the battery interface is defective.
3. If the battery interface is defective, replace
the power management board.
board failure.
No +3.3 V A output 1. Power supply failure 1. Turn off the defibrillator/monitor then
No +3.3 V B output 2. Power management restart it.
board failure. 2. If the problem remains, disconnect the AC
Not +5.0 V output
mains for 5 s and reconnect it, then restart
No +12 V output the defibrillator/ monitor.
3. If the problem still remains, replace the
power management board
NOTE
 When the power module has a failure, it may cause problems to other components,
e.g. the defibrillator/monitor suddenly breaks down during start-up, as the power
module may have a power supply protection. In this case, troubleshoot the power
module per the procedure described in the table above.
 Components of the main unit, SMR and parameter modules are powered by the
power module. In the event that a component malfunctions, check if the operating
voltage is correct. Refer to Chapter2 Theory of Operation for the operating voltage
and measurement points of each component.
6-11

6.6.12 Software Upgrade Probl ems
Boot file upgrade fails Power failure or Return the CPU board to factory for repair.
unintended power off
during boot file upgrade
Program upgrade fails Incorrect network 1. Check that the network cable is properly
connection connected and is not too long (shorter than
50m).
2. Make sure that the network cable is of the
right type. Network cable with crossed wires
inside is used for LAN upgrade and those
with parallel wires inside for WAN.
Wrong upgrade package Upgrade package shall be .pkg files. Select
package according to system requirement
Incorrect IP address Configure a fixed IP address in range C as

configuration specified for the defibrillator/monitor. We
recommend not to upgrade a program when
the defibrillator/monitor is connected to a
network with multiple PCs.
6.7 Technical Alarm Messages

Refer to corresponding chapters in the operating manual.
6-12

6.8 Error Codes
6.8.1 Therapy Module Error Codes

Error codes Error description
0 No error
1 MCU register selftest error
2 MCU RAM selftest error

3 MCU FLASH selftest error
4 MCU watchdog selftest error
5 MCU ADC selftest error
6 DSP register selftest error

7 DSP RAM selftest error
8 DSP FLASH selftest error
9 DSP watchdog selftest error
10 ECG hardware selftest error
11 Power selftest error
12 MCU abnormal reset
13 DSP abnormal reset

14 Computation selftest error
15 to 20 Reserved
21 Impedance circuit error
22 Impedance zeroing failed
23 Impedance calibration failed
24 Impedance measurement is interfered

25 Great measurement difference between two impedance measuring
methods
26 to 30 Reserved
31 Charging is not complete after 25 s
32 Charging is not complete after 30 s
33 Over-charging
34 Charging trend error
35 to 40 Reserved
41 Self-discharging failure
42 IGBT failure
43 Defibrillation relay failure
6-13

Error codes Error description
44 Abnormal discharging current

45 to 70 Reserved
71 Abnormal pacer power
72 Pacer relay failure
73 Pacer frequency error
74 Abnormal pacer current
75 Pacer DA error
76 Pacer voltage error
77 Pacer overcurrent protection point high
78 Pacer overcurrent protection failure

79 to 90 Reserved
91 Comm is interfered (data error)
92 to 99 Reserved
6.8.2 Power Mod ule Error Codes

Error codes Error contents
100/register value Battery permanent failure

101/register value Battery recoverable failure
102 Battery comm error
103 Abnormal battery voltage (not enough voltage)

104 Battery charging failure
105 Power-on selftest error
106 Main control failure (comm handshake overtime)
107 to 199 Reserved
6-14

6.8.3 Main Control Erro r Codes

200 Fan not connected
201 Speaker not connected

202 Storage card does not exist
203 Power board comm error
204 Therapy module comm error
205/register value Main control system power-on selftest error

206 Realtime clock error
207 Storage card read/write error

208 Button board comm error
209 Machine type recognition error

210 Recorder failure (not including thermal printing head overheat)
211 to 299 Reserved
6.8.4 MPM Error Codes

300 DSP CPU failure

301 DSP SDRAM failure
302 DSP FLASH failure

303 DSP watchdog failure
304 7024 CPU failure
305 7024 RAM failure
306 7024 ROM failure
307 7024 A/D failure
308 7024 ECG failure
309 7024 TEMP failure
310 7024 watchdog failure
311 2131 CPU failure
312 2131 RAM failure
313 2131 ROM failure
314 2131 A/D failure
315 2131 watchdog failure
6-15

316 ECG channel 1 failure




324 Mindray SpO2 board CPU failure
325 Mindray SpO2 board RAM failure

326 Mindray SpO2 board ROM failure
327 Mindray SpO2 board A/D failure
328 Mindray SpO2 board watchdog failure
329 NIBP selftest failure (2)

330 NIBP system error (15)
331 to 399 For future use
6-16

7 Disassembly and Repair

7.1 Tools Required
To disassemble and replace the parts and components, the following tools may be required:
 Phillips screwdrivers
 Tweezers
 Sharp nose pliers
 7# Socket wrench
 Adjustable spanner
7-1

7.2 Preparations for Disassembly

Before disassembling the equipment, finish the following preparations:
 Stop patient monitoring and therapy, turn off the equipment and disconnect all the
accessories and peripheral devices.
 Disconnect the AC power source and remove both batteries.
 To avoid high voltage hazard, strictly follow the procedure as defined in section 7.3.6
Discharging the Capacitor for disassembling.
WARNING
 Before disassembling the equipment, be sure to eliminate the static charges first.
When disassembling the parts labeled with static-sensitive symbols, make sure you
are wearing electrostatic discharge protection such as antistatic wristband or
gloves to avoid damaging the equipment.
 Properly connect and route the cables and wires when reassembling the equipment
to avoid short circuit.
 Select appropriate screws to assemble the equipment. If unfit screws are tightened
by force, the equipment may be damaged and the screws or part may fall off
during use, causing unpredictable equipment damage or human injury.
 Follow correct sequence to disassembly the equipment. Otherwise, the equipment

may be damaged permanently.
 Disconnect all the cables before disassembling any parts. Be careful not to damage
any cables or connectors.
 Place removed screws and disassembled parts properly, preventing them from
being lost or contaminated.
 Place the screws and parts from the same module together to facilitate
reassembling.
 To reassemble the equipment, first assemble the assemblies, and then the main
unit. Carefully route the cables.
 Make sure that the waterproof material is properly applied during reassembling.
7-2

7.3 Disassembli ng the Main Unit
WARNING
 To disassemble the equipment, first remove the external assemblies, such as the
hook mount, wireless transmission module,paddle tray and front housing, and then
the internal assemblies and parts.
 The power supply assembly and recorder can be removed without removing any
other assemblies.
 To disassemble the equipment, place the equipment on a work surface free from
foreign material, avoiding damaging the antiglare screen, LCD and the knob. Be
careful not to break the two cotters on the front ends of rear housing.
 All the operations should be performed by qualified service personnel only. Make
sure to put on the insulating gloves during service operations.
 Before remove the therapy module high-voltage board, you must use the dicharge
fixture to discharge the capacitor first. If you do not have a discharge fixture,
disconnect AC mains and remove batteries, Wait for at least 2 hours before
removing the capacitor.
7.3.1 Removing Hook Mount
1. Stand the equipment on the work surface with the back of the equipment facing to you.
Loose and remove the two M3×16 Philips screws; take off the flat washer and spring
washer. Pull out the hooks.
7-3

7.3.2 Remov ing Paddle Tray
1. Stand the equipment on the work surface with the back of the equipment facing to you.
Tweeze the five plastic plugs in the screw holes.
2. Loose and remove the five M3×10 Philips screws. Remove the paddle tray.
3. Make sure that the waterproof strip is properly applied when replacing the paddle tray in
the equipment.
Waterproof strip on
the top of rear case
7-4

7.3.3 Separating the Housin g
1. Lay the equipment on a padded work surface with the display facing down and the
bottom of the equipment nearest to you. Be careful not to damage the LCD and controls.
Loose and remove the 7 M3×10 Philips screws.
2. Stand the equipment on the work surface. Carefully separate the front housing and the
rear housing. Disconnect the cable between the CPU board and keypad board, and then
remove the front housing.
3. Make sure that the waterproof strip is properly applied when reassemble the front
housing.
Cotter
Disconnect this cable

Waterproof strip (in the slot)
7-5

7.3.4 Remov ing the Measurement Modul e Panel
1. Stand the equipment on the work surface. Loose and remove the M3×6 Philips screw
that secures the flexible cable. You can also disconnect the flexible cable by loosening
the plastic nut behind the SpO2 board. Remove the flexible cable.
2. Remove the frame that fastens the measurement module panel.
Fastening
frame
Flexible cable
M3×6 Philips
screws
3. If you equipment is configured with a NIBP module, disconnect the NIBP air tube. If
you equipment is configured with a CO2 module, disconnect the cables between the
CO2 module and the module connector.
 If Mindray CO2 module is configured, disconnect the Nafion tube, CO2 exhaust
tube, micro-active switch connector and flow limit tube.
 If the microstream CO2 module is configured, disconnect the CO2 exhaust tube
and remove the CO2 connector assembly. If the connector assembly is difficult to
be removed, disconnect the air tube and cable on it. Take care not to damage the air
tube and cables. Remove the measurement module panel.
 Mindray CO2 module
Nafion tube
NIBP air tub
CO2 exhaust tube
Flow limit tube
Micro-active switch connector
7-6

 Microstream CO2 module
NIBP air tube
CO2 exhaust tube
Microstream
CO2 connector
NOTE
 Be careful not to damage the air tube when disconnecting the air tube or the cable
between the CO2 module and the module connector. During reassembly, route the
air tube and cable so that they are placed between the MPM module and CO2
module, making sure not to block the air tube.
 When replacing the measurement module panel, do not screw the flexible cable
forcibly avoiding screw slipping. In case the screw slips, fasten the plastic bolt with
the nut before screwing.
 When the equipment is reassembled, make sure that the frame securing the
measurement module panel does not bend the two cotters on the rear housing.
7-7

7.3.5 Removing the Power Supply Assembl y
1. Lay the equipment on a padded work surface with the display side facing down and the
bottom of the equipment nearest to you. Be careful not to break the two cotters in the
front of rear housing. Loose and remove the two M3×8 Philips screws and pull out the
power supply assembly.
Protect the cotters in the front of rear

housing from breaking when removing
the two screws.
M3×8 Philips
screws
2. Disconnect the cable between the power management board and AC/DC module.
Remove the Power Supply Assembly.
Cable between the power management

board and AC/DC module
Make sure to place the cable near the

rear case when replacing the power
supply assembly.
7-8

7.3.6 Dischargin g the Capacit or
WARNING
 Before removing the capacitor, you must wear insulation gloves which stand high
voltage.
1. Use the high-voltage discharge fixture (0651-TF11) to disarm the capacitor by hooking
the high-voltage ground (TP1) with the black probe of the fixture, and hooking the
high-voltage socket (TP3) with the fixture’s red probe. Wait till the indicating lamp on
the fixture turns off. The capacitor is not completely discharged if the indicator remains
on.
2. Set the multimeter to DC 1000V. Measure the discharge resistance to check if the
reading of the multimeter is lower than 30V. If yes, you can safely disassemble the
equipment now.
TP1 TP3
7-9

7.3.7 Removing the Therapy Modul e High-voltage Bo ard
1. Disconnect the cables from the therapy port and the capacitor.
2. Loose and remove the six M4×8 Philips screws. Remove the therapy module
high-voltage board.
High-voltag
M4×8
e board
Philips screw
Therapy port cable

Capacitor
cable
WARNING
 Before remove the therapy module high-voltage board, you must use the dicharge
fixture to discharge the capacitor first. If you do not have a discharge fixture,
disconnect AC mains and remove batteries, Wait for at least 2 hours before
removing the capacitor.
NOTE
 When replacing the therapy module low-voltage and high-voltage boards, carefully
route the cable to the therapy port so that it comes out through the gaps of PBCAs
and insulation sheet. Make sure the cable is not pressed by the PCBAs.
 Route the cables, making sure that the cables are placed in the gaps between the
PCBAs.
 When connecting two PCBAs, align the connectors and make sure they are firmly
engaged.
7-10

7.3.8 Disassembling the MPM Modul e
1. Stand the equipment on the work surface, and remove the four M4×8 Philips screws. If
your MPM module has a fan on it, first disconnect the fan cable, and then remove the
four M4×8 Philips screws.
M4×8
Philips screws
2. Disconnect the MPM cable and remove the MPM module assembly.
MPM module
assembly
MPM cable
7-11

7.3.9 Removin g t he CO2 Modu le
1. Stand the equipment. Remove the 2 screws integrated with the left capacitor sheet metal
and the two M3×8 Philips screws. Remove the sheet metal and the CO2 module, if it is
configured. Remove the left capacitor.
Screws integra
ted with the
sheet metal
Left capacitor
sheet metal
M3X8 Philips
screws
7.3.10 Removi ng t he CPU board As sembl y
1. Remove the insulation sheet for the power management board. Pull out the magnetic
ring. Disconnect the cable between the power management board and keypad board.
2. Remove the six M4×20 blots and the two M3×8 Philips screws; remove the CPU board
assembly. To remove the data card, remove the M4×10 socket head screw.
M3×8 Philips
screws
For replacement,
place the magnetic
ring in the gap
between PCBAs
and rear case
When reassembling, first

M4×10 socket pass this cable through the
head screws gap of rear housing
M4×20 bolt screws
7-12

3. Remove the 4 M3×6 Philips screws. Separate the CPU board and power management
board.
M3×6 Philips
screws
CPU board
NOTE
 To reassemble the CPU board assembly, pass the cable between the power
management board and AC/DC module through the gap on the rear housing; then
replace the CPU board assembly.
 Carefully route the therapy port cable so that it comes out through the gap of
PBCA. Be careful not to press the cable under the PCBA. Make sure the magnetic
ring is fixed at the gap of the CPU board and rear housing.
7.3.11 Removing the Therapy Port Ass embly

Pull the therapy port upward and remove the therapy port assembly
Therapy port latch
7-13

7.3.12 Checking Waterproof Material on the Rear Housing

Before reassembling the equipment, make sure that the waterproof material on the rear
housing are stuck to the proper places.
1. Check that the battery elastic pad and the silicone pad are stuck in place.
Silicone
pads. Apply
Battery
glue here
elastic pad
before close
the rear case.
2. Check that power supply waterproof pads 1, 2 and 3 are stuck in place.
Power supply waterproof pad 1
Power supply
waterproof pad 3
Power supply waterproof pad
3. Check that the white waterproof strip is adhered to the proper place.
White waterproof
strip (45 cm long)
7-14

7.4 Disassembling the Front Housin g Assembly
NOTE
 To disassemble the equipment, place the equipment on a work surface free from
foreign material, avoiding damaging the antiglare screen, LCD and the knobs.
 After repairing any other front housing assembly, verify that the speaker is not
damaged by powering on the equipment and testing the speaker.
 Clear the LCD before replace it.
7.4.1 Removing the Keypad board
1. Cut the cable tie. Remove the seven M3×8 Philips screws and remove the front housing
sheet metal.
Front housing
metal sheet
M3×8
Philips screws
Cut the cable tie
7-15

2. Disconnect all the cables. Before disconnecting the rotary encoder cable, remove the
hot-melt glue using the sharp nose pliers.
When reassembling,
apply hot-melt glue to
the cable connector
Encoder cable
3. Remove the eight M3×8 Philips screws and remove the keypad board.
M3×8
Philips screws
NOTE
 When reassembling the equipment, apply hot-melt glue to the rotary encoder’s
cable connector to help fastening the cable. Be careful not to damage the cables and
connectors when plugging and unplugging the cables. Properly route the cables
7-16

7.4.2 Removing Display As sembly
1. Disconnect the cables from the alarm lamp board and the indicating lamp board. Your
equipment may be configured with a Toshiba LCD, or Sharp LCD, or AU LCD.
Alarm lamp board cable

Alarm lamp board cable
LED board cable LED board cable
Toshiba LCD Sharp LCD
Alarm lamp
board cable
Mode
Select knob
LED board cable
AU LCD
7-17

2. Remove the display assembly from the front housing, Remove the LCD from the shield;
disconnect the cables; remove the LCD inverter.
Sharp LCD inverter

Toshiba LCD inverter
LCD cable Cable between LCD cable

Cable between
the inverter and
the inverter and
keypad board
keypad board
AU LCD
AU LCD
backlight board
Magnetic ring
between the inverter
and keypad board
LCD
NOTE
 If Sharp LCD is configured, S15 on the keypad board should be short (soldering
temperature between 280 and 300 , soldering time no more than 3 seconds), as
shown below. If Toshiba or AU LCD is configured, the S15 should be open.
7-18

Sharp LCD:
S15 is short
3. Disconnect the cables and separate the LCD from the rubber frame.
For Toshiba or AU
For Sharp LCD,
LCD, inverter cable
inverter cable passes
passes through this gap
through this gap.
Using hot-melt glue to

help fixing the cable to
the connector.
LCD cable
NOTE
 Be careful not to damage the rubber frame. Properly route the cables.
 Protect the antiglare screen, LCD and the rotary knob from being scratched.
 When reassembling the equipment, apply hot-melt glue to the display’s cable
connector to help fastening the cable.
7-19

7.4.3 Remov ing the Speaker
1. Remove the two M3×8 Philips screws. Take off the speaker bracket, and then remove
the speaker.
2. After repairing any other front housing assembly, verify that the speaker is not damaged
by powering on the equipment and testing the speaker.
M3×8 Philips
screws.
7.4.4 Removing the Indicatin g Lamp Board and Alarm L amp
Board
To remove the alarm lamp board and indicating lamp board, remove the three M3×8 Philips
screws. Then you can remove the alarm lamp shade and indicating lamp shade.
Alarm lamp board

I
n
d
i
c
a
t
i Alarm lamp
n
Apply glue (DP-10
shade
g
5) at the snaps
l
M3×8 Philips
a
m
p
screws b
o
a
r
d
,
7-20

7.4.5 Removing t he Mode Select Knob
1. Use a sharp nose pliers to pull the Mode Select knob off its shaft. Loosen and remove
the nut and washer using a socket wrench. Disconnect the cable from the knob.
Knob
cable
Washer
and nut
with the
knob
Check that the

knob is aligned
with the labeling.
NOTE
 When replacing the Mode Select knob, check that it is aligned with the labeling.
Adjusting the knob using sharp nose pliers if necessary.
7-21

7.4.6 Removing the Rotary Encoder
1. Pull the encoder off its shaft. Loosen and remove the nut and washer using a socket
wrench. Disconnect the encoder cable.
Encoder
cable
Washer and
nut with the
encoder
Rotary
encoder
7.4.7 Removi ng t he Recorder
1. Remove the two M3×6 Philips screws. Pull the recorder out of the recorder well.
Disconnect the cable from the recorder, and then remove the recorder.
Recorder
cable
M3×6 Philips
screws
7-22

7.5 Disassembli ng the MPM Module
NOTE
 Take care not to damage the plastic bolts and nuts when disassembling and
replacing the PCBAs of the MPM module.
 The MPM module can be flexibly configured according to the customer’s

requirements. Make sure correct PCBAs are used when reassembling the MPM
module.
7.5.1 Remov ing the Fan

Remove the two M3×14 Philips screws and the φ3 flat washer. Then remove the fan.
M3×14 Philips
screws with φ3
flat washer
NOTE
 The new MPM module does not have a fan. For MPM module which is equipped
with a fan, remember to install the fan during reassembling the MPM module after
maintenance or upgrade.
7-23

7.5.2 Removi ng the SpO2 board
1. If your equipment is configured with a Masimo SpO2 module, remove the three M3×14
Philips screws. Thus you can remove the Masimo SpO2 board, Masimo SpO2 adapter
board and Masimo PCBA stacking sleeves.
Masimo SpO2 board
Masimo PCBA Masimo SpO2

M3×14 Philips
stacking sleeves adapter board
screws
2. If your equipment is configured with a Nellcor or Mindray SpO2 module, remove the
three M3×6 Philips screws. Thus you can remove the Nellcor or Mindray SpO2 module.
M3×6 Philips screws

Nellcor SpO2 board Mindray SpO2 board
NOTE
 If 9008 Mindray SpO2 board (051-000058-00) is configured, check SpO2 board

jumper before reassembly. The S3 and S4 should be short, while S5 should be
open. The soldering temperature should be between 280 and 300 , and soldering
time should be no more than 3 seconds
7-24

7.5.3 Removi ng t he MPM Modul e Analog Board
1. If your equipment is configured with the SpO2 module, remove the three M3×6 Philips
screws and a M3×12 plastic bolt. Remove the MPM module analog board.
M3×12 plastic
bolt M3×6 Philips
screws
Analog board
2. If your equipment is not configured with the SpO2 module, remove the three M3×6
Philips screws. Then you can remove the MPM module analog board.
M3×6 Philips
screws
7-25

7.5.4 Removi ng t he MPM Modu le Digital Board
1. Remove the 3 M3×15+6-8 plastic bolt and a M3×6 Philips screw. If your equipment is
configured with the NIBP module, disconnect the cable and then remove the MPM
module digital board.
M3×6 Philips
screws
MPM module
M3X15+6-8 digital board
plastic bolt
and insulation
flat washer
Dumping valve cable Linear valve cable
Pump
cable
3×100 mm cable tie
7-26

7.5.5 Removin g t he NIBP Module

Cut the cable ties. Disconnect the air tubing; remove the pump and airway connector.
Remove the four nuts; then you can remove the NIBP valves shield and the dumping and
linear valves.
NIBP valves
shield
Pump
Airway
connector
Dumping valve (blue

and black wires)
Linear valve
(white & black wires)
7-27

7.6 Disassembling th e Power Supply Assembly
7.6.1 Remov ing the AC/DC board
Remove the seven M3×6 Philips screws. Disconnect the cable from the AC power input and
remove the AC/DC board.
AC power input
cable
7-28

7.6.2 Removi ng t he Power Supply Sheet Metal and the
Grounding Terminal
1. Remove the M3×6 Philips screw; disconnect the ground wire. Remove the M6 nut; the
power supply metal sheet; the φ6 flat washer and the M6 nut in turn. Then you can
remove the grounding terminal.
Power supply
metal sheet
M6 nut
Ground wire
M3×6 Philips screw

+ washer
φ6 flat washer
+ M6 nut
2. Make sure that the waterproof pad is properly applied when replacing the power supply
module.
Power module
waterproof pad 1
7-29

7.7 Disassembli ng the CO2 Module
7.7.1 Disassembling the Microstream CO2 Module
1. Remove the six M3×6 Philips screws, and then remove the microstream CO2 module
and the CO2 adapter board.
Microstream Microstream
CO2 adapter CO2 module
board
Bolt
M3X7+8-6
7-30

7.7.2 Disass embli ng Min dray CO2 Module
1. Remove the four M3×6 Philips screws, and then remove the Mindray CO2 module.
M3×6 Philips
CO2 module
screws
(M02B)
Bolt
M3X7+8-6
7-31

7.8 Disassembling the Measur ement Module Panel
Assembly
7.8.1 Disassembling the Measurement Module Panel with
Mindr ay CO2 Module
1. Remove the two PT2×6 crosshead tapping screws; take out the watertrap receptacle.
Watertrap
Receptacle kit
PT2×6 crosshead
tapping screw
2. Remove the four PT2×6 crosshead tapping screws. Thus you can remove the watertrap
bracket.
Watertrap bracket
PT2×6 crosshead
tapping screw
NOTE
 Make sure the waterproof sheet is properly applied when replacing the CO2
module in the equipment.
7-32

7.8.2 Disassembling the Measurement Module Panel with
Microstream CO2 Module

To remove the CO2 connector, peel the waterproof sheet and loose the four snaps.
Loose the
4 snaps
Microstream
CO2 connector
Waterproof
sheet
7.8.3 Disassembling the Measur ement Module Panel wit hout
CO2 Module
1. Remove the four PT2×6 crosshead tapping screws, and then remove the CO2
compartment door.
PT2×6 cross head

tapping screws
CO2
compartment
door
2. Make sure the waterproof sheet is properly applied when replacing the CO2 module in
the equipment.
Waterproof sheet
7-33

7.9 Disassembling the Recor der
7.9.1 Disassembling t he TR6F Recorder
1. Loosen the two snaps and remove the recorder drive board.
Snaps
Recorder drive board
2. Loosen and remove the two PT2×6 crosshead tapping screws. Disconnect the flexible
cable and the connection cable between the recorder drive board and recorder keypad
board. Remove the thermal print head and recorder drive board.
Thermal
print head PT2×6 crosshead
tapping screw
Cable between
Flexible cable the recorder
drive board and
recorder keypad
board
7-34

3. Remove the two PT2×6 crosshead tapping screws, and then remove the keypad board.
PT2×6 crosshead
tapping screw
Keypad board
7.9.2 Disass embli ng t he TR8A Recorder
1. Remove the two M3×8 Philips screws.
M3×8 Philips
screws
Recorder drive
board
2. Disconnect the flexible cable and the connection cable between the recorder drive board
and recorder keypad board. Remove the recorder drive board.
Cable between the

recorder drive board
Flexible cable
and recorder
keypad board
7-35

3. Remove the two PT2×6 crosshead tapping screws; take out the print head.
Print head
PT2.6×6 crosshead
mounting
tapping screws
plate
4. Remove the two M2×4 Philips screws and then remove the print head.
5. Remove the two PT2×6 crosshead tapping screws, and then remove the keypad board.
Keypad board
PT2×6 crosshead
tapping screws
7-36

7.10 Disassembling the Extern al Paddle
7.10.1 Disassembling the Adult Paddle

Press the latch and slide the adult paddle in the direction as indicated by the following figure
until it is removed.
Press the latch
7.10.2 Disassembling the Apex Pediatric Paddle
1. Peel up the labels
Sternum Apex paddle

paddle label labels
2. Remove the two PT3×14 crosshead tapping screws; and then remove the handle cover
and the P+R button.
Be sure to install the waterproof

Apex paddle
strip when reassembling the paddle
cover
PT3×14 crosshead Apex paddle P+R button

tapping screws
7-37

3. Remove the PT3×14 crosshead tapping screw. Take off the button bracket; disconnect
the cable and remove the keypad board.
Apex paddle
button bracket
PT3×14 crosshead Apex paddle

tapping screw keypad board
7.10.3 Disassembling the Sternum Pediatric Paddle
1. Remove the two PT3×14 crosshead tapping screws; remove the handle cover and then
the P+R button.
Sternum Sternum paddle

paddle cover P+R button
PT3×14 Apply the water proof strip when

tapping screws reassembling paddle cover
2. Remove the PT3×14 crosshead tapping screw. Take off the button bracket; disconnect
the cable and remove the keypad board.
Sternum paddle
button bracket
PT3×14 crosshead Sternum paddle

tapping screw keypad board
7-38

8 Parts
8.1 Introductio n
This chapter contains the equipment’s exploded views and parts lists. It helps the engineer to
identify the parts during disassembling the equipment and replacing the parts. This manual is
based on the maximum configuration. Your equipment may not have some parts and the
quantity of the screws, stacking sleeves, and etc may be different with those included in the
parts lists.
The figure below shows the hardware architecture of the equipment’s main unit.
Main Unit
Front housing Rear housing Paddle tray Other

assembly assembly assembly assemblies
External
Front housing Rear housing Paddle tray
paddle set
Handle kit Lithium

Anti-glare screen Power base assembly
battery
Paddle holding Hook mount

8.4" LCD Main board assembly
reed kit
Handle reinforce
Mode Select knob MPM module
sheet metal
Therapy module Paddle sheet

Navigation knob
assembly metal
Recorder Therapy port assembly
Alarm lamp shade CO2 module
Measurement module
Keypad board
panel assembly
Inverter Capacitor assembly
Speaker
Indicating lamp shade
Alarm lamp board
Indicating lamp board
8-1

8.2 Main Unit
8.2.1 Exploded View
8.2.2 Parts List

SN P/N Description Qty
801-0651-00006-00 External paddle set (Chinese)

801-0651-00010-00 External paddle set (English)
801-0651-00101-00 External paddle set (Spanish)
External paddle set

801-0651-00102-00
(German/French/Dutch) 1
1
801-0651-00103-00 External paddle set (Polish) (As configured)
801-0651-00105-00 External paddle set (Italian)
801-0651-00106-00 External paddle set (Turkish)
801-0651-00107-00 External paddle set (Russian)
801-0651-00108-00 External paddle set (Brazil Portuguese)
8-2

2 801-0651-00037-00 Paddle tray assembly 1
3 / Philips screw, M3×10 12
4 / Plastic plug 5
5 / Handle mounting plate 1
6 801-0651-00005-00 Hook mount kit 1
7 / Flat washer 2
8 / Spring washer 2
10 022-000012-00 Lithium batteries 2
11 / Rear housing assembly 1
12 / Silicone tube 1
13 / Front housing assembly 1
8-3

8.3 Front Housing Assembly
8.3.1 Exploded View
8.3.2 Parts List

/ Front housing sheet metal 1

1
/ Front housing sheet metal (Sharp) (As configured)
3 801-0651-00026-00 Keypad board 1
4 1
0651-20-76783-51 Silicone keypad (Chinese), monitoring
8-4

area
Silicone keypad (English), monitoring

0651-20-76783-52
area
049-000091-00 Silicone keypad (Spanish)
049-000092-00 Silicone keypad (German)
049-000093-00 Silicone keypad (Polish)

(As configured)
049-000094-00 Silicone keypad (French)
049-000095-00 Silicone keypad (Italian)
049-000097-00 Silicone keypad (Russian)
049-000098-00 Silicone keypad (Brazil Portuguese)
049-000096-00 Silicone keypad (Turkish)
049-000099-00 Silicone keypad (Dutch)
5 0651-20-76782-51 Silicone keypad, defibrillation 1
801-0000-00002-00 Inverter, DC/AC 12VDC 500Vrms 6mA 1

6
801-0000-00007-00 Inverter, DC/AC12VDC/600Vrms 6mA (As configured)
7 / Conductive foam, 4105AB51K 1
/ Silicone frame for LCD 1

8
/ Silicone frame for LCD (Sharp) (As configured)
801-0651-00111-00 LCD, Sharp 1

9
801-0651-00138-00 LCD, AU (As configured)
10 / Reed, 92-047 1
11 / LCD shield 1
12 / Antiglare screen 1
Antiglare screen double-sided adhesive

13 / 2
PET1
Antiglare screen double-sided adhesive

14 / 2
PET2
Optical Encorder, 16 positions, 5VDC

15 801-0651-00044-00 1
Dip6
16 / Knob waterproof pad 1
17 801-0651-00043-00 Mode Select knob cable 1
18 / Torsion spring, 1707P 2
19 / Mode Select knob 1

Mode label(D6, Chinese, with pacer 1
20 /
function) (As configured)
8-5

Mode label (D6, English, with pacer

/
function)
Mode label (D6, Chinese, without pacer
/
function)
Mode label (D6, English, without pacer
/
function)
Mode label (D6, Spanish, with pacer
/
function)
Mode label (D6, Spanish, without pacer
/
function)
Mode label (D6, German, with pacer
/
function)
Mode label (D6, Chin German, without
/
pacer function)
Mode label (D6, Polish, with pacer
/
function)
Mode label (D6, Polish, without pacer
/
function)
Mode label (D6, French, with pacer
/
function)
Mode label (D6, French, without pacer
/
function)
Mode label (D6, Italian, with pacer
/
function)
Mode label (D6, Italian, without pacer
/
function)
Mode label (D6, Turkish, with pacer
/
function)
Mode label (D6, Turkish, without pacer
/
function)
Mode label (D6, Russian, with pacer
/
function)
Mode label (D6, Russian, without pacer
/
function)
Mode label (D6, (Brazil Portuguese, with
/
pacer function)
Mode label (D6, (Brazil Portuguese,
/
without pacer function)
Mode label (D6, Dutch, with pacer
/
function)
Mode label (D6, Dutch, without pacer
/
function)
21 / Navigation knob 1
TR6F-30-67306 TR6F recorder 1

22
115-008103-00 TR8A recorder (As configured)
8-6

23 / Alarm indicating lamp 1
24 / Recorder frame 1
25 801-0651-00047-00 Front panel (D6) 1
26 / Speaker seal pad 1
27 020-000004-00 Speaker 1
28 / Indicator shade 1
29 801-0651-00032-00 Alarm light board 1
30 801-0651-00027-00 Indicator board 1
31 / Speaker pad 2
32 / Speaker mounting plate 1
33 / Conductive cloth pad 2
Insulation plate for front housing sheet

34 / 1
metal
8-7

8.4 Rear Housin g Assembly
8.4.1 Exploded View
8.4.2 Parts List

1 801-0651-00038-00 Power base assembly 1

2 801-0651-00141-00 Rear housing assembly 1
3 009-001325-00 Therapy port cable 1
4 / Therapy port waterproof pad 1
5 801-0651-00033-00 Main board assembly 1
6 043-001116-00 Therapy port latch 1
7 / Bolt, M4×20_7-8 6
8-8

8 / Power management board insulation sheet 1

9 801-0652-00033-00 Therapy module kit (with pacer) (FRU) 1
801-0652-00034-00 Therapy module kit (no pacer) (As configured)
10 042-005519-00 Right bracket 1
13 801-0651-00040-00 Capacitor assembly 1
M02B-30-64513 CO2 module (M02B) 1,
14
801-0651-00078-00 Microstream CO2 module (As configured)
801-0651-00009-00 MPM module, without NIBP module

801-0651-00012-00 MPM module (Mindray SpO2 module)
801-0651-00013-00 MPM module (Masimo SpO2 module )
801-0651-00014-00 MPM module (Nellcor SpO2 module )
801-0651-00015-00 MPM module (NIBP)
801-0651-00016-00 MPM module (NIBP/Mindray SpO2) 1
15
801-0651-00017-00 MPM module (NIBP/Masimo SpO2) (As configured)
801-0651-00018-00 MPM module (NIBP/Nellcor SpO2)
801-0651-00116-00 12-lead upgrade kit (FRU)
MPM module, without NIBP module
801-0651-00119-00
(FRU)
801-0651-00120-00 MPM module (Mindray SpO2 module)
Frame for fastening the measurement
16 / 1
module panel
Measurement module panel assembly
801-0651-00019-00
(Mindray SpO2)
Measurement module panel assembly 1

18 801-0651-00020-00
(Masimo SpO2) (As configured)
Measurement module panel assembly
801-0651-00021-00
(Nellcor SpO2)
19 801-0652-00027-00 On-position detection switch 1
8-9

8.5 Rear Housing
8.5.1 Exploded View
8-10

8.5.2 Parts List

1 / Handle mounting plate 2
2 / MPM connector lock pad 1
1
3 / Warning label 2
(As configured)
1
4 Instruction label
/ (As configured)
5 / Silicone pad 2
Stainless steel socket head screw,

6
/ M4×10 1
7 / Wall mount reinforce metal 2
8 043-001936-00 Rear housing 1
9 / Stainless steel screw, M3×8 1
10 / Handle reinforce sheet metal 1
11 / Battery elastic pad 2
1
12 /
BeneHeart D6 main unit label (As configured)
13 / Service label 1
14 / Power supply waterproof pad 1 2
17 / Foot pad (0651) 5
18 / Electrode spring 2
8-11

8.6 Measurement Module Panel Assembly
8.6.1 Exploded View
8.6.2 Parts List

1 / Measurement module panel 1
2 / MPM module IBP connector 2
3 / MPM module TEMP connector 2
4 / MPM module SpO2 connector 1
5 / Flexible cable for Mindray SpO2 module 1
6 / FPC mounting plate 1
7 / FPC insulation sheet 1
8-12

Stainless steel crosshead tapping screws,

8 / 4
PT3×10
9 / MPM module ECG connector 1
10 / CO2 connector waterproof sheet 1
11 / NIBP connector 1
12 / Stainless steel nut, GB6170 M5 1
13 / IBP dummy connector 1
14 / Gas outlet 1
Measurement module overlay

/
(ECG+SpO2+NIBP+2 IBP+TEMP+CO2)

/ (ECG+NIBP)

/
(ECG+SpO2)

/
(ECG+SpO2+NIBP+TEMP)

1
15 / (ECG+SpO2+NIBP+2 IBP+TEMP)
(As configured)
/
(ECG+CO2)

/
(ECG+NIBP+CO2)

/
(ECG+SpO2+CO2)

/ (ECG+SpO2+NIBP+TEMP+CO2)
/ Measurement module overlay (ECG)
16 / Watertrap bracket 1
17 / Crosshead tapping screws, PT2.0×6 6
801-0651-00042-00 Watertrap receptacle 1

18
9201-30-35923 Microstream CO2 connector assembly (As configured)

8-13

8.7 Power Suppl y As sembly
8.7.1 Exploded View
8-14

8.7.2 Parts List

1 801-0651-00041-00 Power seat (0651) 1

2 / Grounding terminal 1
3 / Lock washer, GB/T862.2-1987 6 1
4 / Power supply metal sheet 1
5 / Hexagon nut, GB/T6172-1986 M6 2

6 / Flat washer, GB97.1 6 1
7 / AC PCB insulation sheet 1

9 / AC heat conduction glue 3
10 801-0651-00024-00 AC/DC board (RFU) 1
11 / AC mains label 1
12 / AC plug protection hook 1

13 / AC power input cable 1
14 / Power module waterproof pad 1 2

15 / Power module waterproof pad 2 2
8-15

8.8 MPM Module
8.8.1 Exploded View
8-16

8.8.2 Parts List

801-0651-00022-00 MPM module Mindray SpO2 board (FRU)

1
1 801-0651-00088-00 Nellcor SpO2 board (FRU)
(As configured)
0010-10-12275 Masimo M7 Board
801-0651-00002-00 MPM module analog board, Mindray (FRU)
801-0651-00003-00 MPM module analog board, Nellcor (FRU)

1
2 801-0651-00004-00 MPM module analog board, Masimo (FRU)
(As configured)
MPM module analog board,
801-0651-00085-00
Mindray/defibrillator (FRU)
1
2a 801-0651-00023-00 MPM module Masimo SpO2 adapter board (for Masimo
SpO2 board)
MPM module digital board (lead-free process,
801-0651-00001-00
FRU) 1
3
MPM module digital board (lead-free (As configured)
801-0651-00086-00
process/defibrillator, FRU)
4 / Plastic hexagon bolt, M3×15+6-8 3
5 / Gas pump, P16B07 1

6 / 6800 Fast release valve assembly 1
7 / Insulating plate 1
9 / MPM socket cushion 1
10 / MPM module connector fixer 1
11 / MPM module sheet metal 1
12 / 6800 Slow release valve assembly 1
13 / NIBP valves shield 1

14 / Bolt, M3×16+8-8 3
15 / Hexagon nut and lock washer kit, M3 5
16 / Spring washer 1
17 / Bolt, M3×14+8-10 1

19 / 12-lead ECG board fixer 2 1
20 / 12-lead ECG board 1
21 / 12-lead ECG board fixer 1 1
8-17

8.9 Capacitor Assembly
8.9.1 Exploded View
8.9.2 Parts List

1 / Capacitor pad 2 1
2 / Phase I capacitor cable 1

3 / Capacitor protective layer 1
4 / Capacitor pad 1 1
8-18

8.10 Sidestream CO2 Module Kit
8.10.1 Exploded View
8.10.2 Parts Lis t

SN P/N Description Qty Remark
1 / Philips screw, M3×6 4 /

2 M02B-30-64513 CO2 main unit (M02B) 1 /
3 / Bolt, M3×7+8-6 2 /
4 / Left capacitor sheet metal 1 /
5 / Conductive foam 1 /
Parts that are included in the sidestream CO2 module kit, but not shown in above figure:
/ Gas outlet 1
/ Watertrap bracket 1
Refer to the figure
801-0651-00042-00 Watertrap receptacle assembly 1
of measurement
Stainless steel hexagon nut, module panel for
/ 1
GB/T6170-2000 M5 assembly
Crosshead tapping screws,
/ 4
PT2.0×6
8-19

8.11 Microstr eam CO2 Module Kit
8.11.2 Parts Lis t

SN P/N Description Qty Remark
1 / Philips screw, M3×6 6 /
2 Microstream CO2 connector assembly 1 /

3 9201-30-35908 Microstream CO2 module 1 /
4 801-0651-00078-00 Bolt, M3×7+8-6 5 /

5 / Left capacitor sheet metal 1 /
6 / Conductive foam / /
Parts that are included in the microstream CO2 module kit, but not shown in above figure:
/ Gas outlet 1 Refer to the
Stainless steel hexagon nut, figure of

/ 1 measurement
GB/T6170-2000 M5
module
9201-30-35923 Microstream CO2 module receptacle fixer 1 panel for

assembly
/ Crosshead tapping screws, PT2.0×6 4
8-20

8.12 Paddle Tray Assembly
8.12.2 Parts Lis t

1 / Paddle tray 1
2 / Paddle fixing leaf 4
3 / Sternum paddle discharge metal 1
4 / Silicon pressing plate 2
5 / Travel switch insulation plate 1

7 / Apex paddle discharge metal 1

8 / Tapping screw, PT3×10 2
9 / Spring washer 2
10 / Flat washer 2
12 / Spring washer 2
13 / Flat washer 2
14 801-0651-00124-00 Test load cable 1
15 0651-21-77162 Handle (0651) 1
8-21

8.13 Extern al Paddle
8.13.2 Parts Lis t
1 / Sternum pediatric paddle kit 1

2 / Sternum adult paddle kit 1
3 / Apex pediatric paddle kit 1
4 / Apex adult paddle kit 1
5 / External paddle cable 1
8-22

8.14 Sternum Pediatric Paddle Kit
8.14.2 Parts Lis t

0651-20-76818-51 Sternum paddle label (Chinese)

047-001597-00 Sternum paddle label (Spanish)
Sternum paddle label
047-001598-00
(German/French/Turkish/Dutch)
047-001599-00 Sternum paddle label (Polish) 1
1
047-001601-00 Sternum paddle label (Italian) (As configured)
047-001603-00 Sternum paddle label (Russian)
Sternum paddle label (Brazil
047-001604-00
Portuguese)
0651-20-76818-52 Sternum paddle label (English)
2 / Tapping screw, PT3×14 3
3 / Sternum paddle handle cover 1
5 / Pediatric paddle electrode 1
6 / Pediatric paddle electrode EVA pad 1
7 / Sternum pediatric paddle base (0651) 1
8 / Sternum paddle keypad board 1
9 / Sternum paddle button bracket 1
10 / Sternum paddle P+R button 1
8-23

8.15 Sternum Adult Paddle Kit
8.15.2 Parts Lis t

1 / Sternum adult paddle base 1
2 / Adult paddle labeling 1

3 / Paddle push bar reed 1
4 / Paddle push bar 1

5 / Adult paddle electrode 1
6 / Adult paddle double-sided sticker 1
8-24

8.16 Apex Pediatric Paddle Kit
8.16.2 Parts Lis t

0651-20-76849-51 Apex paddle label (Chinese)

Apex paddle label
1
047-001607-00 (German/Spanish/French/Dutch/Brazil
portuguese) 1
047-001608-00 Apex paddle label (Chinese) (As configured)
047-001610-00 Apex paddle label (Chinese)
047-001611-00 Apex paddle label (Chinese)
047-001612-00 Apex paddle label (English)
2 / Philips screw, PT3×14 3
3 / Apex paddle handle cover 1
5 / Pediatric paddle electrode 1
6 / Pediatric paddle electrode EVA pad 1
7 / Apex pediatric paddle base (0651) 1
8 801-0651-00029-00 Apex paddle keypad board 1
9 / Apex paddle button bracket 1
/ Apex paddle P+R button (Chinese)
10 1 (As configured)
/ Apex paddle P+R button
8-25

8.17 Apex Adult Paddle Kit
8.17.2 Parts Lis t

1 / Apex adult paddle base 1

2 / adult paddle labelling 2
3 / Paddle push bar reed 1
4 / Paddle push bar 1
5 / Adult paddle electrode 1
8-26

8.18 Extern al Paddle Cable
8.18.2 Parts Lis t

1 / Paddle cable connector 1

2 / Torsion spring 1
3 / Connector lock (0651) 1
4 / Silicone pad 1
5 / Paddle cable 1
6 / Sternum paddle cable anchorage 1
7 / Apex paddle cable anchorage 1
8-27

8.19 Hook Mount
8.19.2 Parts Lis t

1 / Hook 2
2 / Pin 2
3 / Spring 2
4 / Hook base 1
5 / Sleeve 2
8-28

8.20 Replacement Parts
To replace parts, refer to 5 Disassembly and Repair and the explosive views above.
NOTE
 Here we list most replacement parts. If you need more parts, please contact our
Customer Service Department.
8.20.1 Main Unit

P/N Description Qty
Front housing
801-0651-00026-00 Keypad board

0651-20-76783-51 Silicone keypad (Chinese), monitoring area
0651-20-76783-52 Silicone keypad (English), monitoring area

049-000091-00 Silicone keypad (Spanish), monitoring area
049-000092-00 Silicone keypad (German), monitoring area

049-000093-00 Silicone keypad (Porlish), monitoring area
1
049-000094-00 Silicone keypad (French), monitoring area
(As configured)
049-000095-00 Silicone keypad (Italian), monitoring area
049-000097-00 Silicone keypad (Russian), monitoring area

Silicone keypad (Brazil Portuguese), monitoring
049-000098-00
area
049-000096-00 Silicone keypad (Turkish), monitoring area
049-000099-00 Silicone keypad (Dutch), monitoring area
0651-20-76782-51 Silicone keypad, defibrillation 1

801-0000-00002-00 Inverter, DC/AC, 12VDC 500Vrms 6mA 1
801-0000-00007-00 Inverter, DC/AC, 12VDC 600Vrms 6mA 1

801-0651-00111-00 Sharp LCD
801-0651-00110-00 Toshiba LCD 1
801-0651-00138-00 AU LCD (As configured)
801-0651-00044-00 Rotating encoder

801-0651-00043-00 Mode Select knob 1
801-0651-00047-00 Front housing (D6) 1
020-000004-00 Speaker, 8ohm, 1W 40 (dia)*6.8 (hgt) mm 1
8-29

P/N Description Qty
801-0000-00032-00 Alarm lamp board 1

801-0000-00027-00 Indicating lamp board 1
Rear housing
801-0651-00038-00 Power base assembly 1

801-0651-00141-00 Rear housing assembly 1
801-0651-00040-00 Capacitor assembly 2
801-0651-00078-00 Microstream CO2 module kit 1
801-0651-00039-00 Therapy port assembly (FRU) 1

801-0651-00046-00 LCD assembly (Sharp LCD)
1
801-0651-00045-00 LCD assembly (AU LCD)
(As configured)
801-0651-00083-00 LCD assembly (Toshiba LCD, FRU)
801-0651-00025-00 Power management board (FRU) 1
801-0652-00027-00 On-position detection switch 1

801-0652-00031-00 Therapy module (no pacer) (FRU) 1
801-0652-00032-00 Therapy module (with pacer) (FRU) 1

801-0652-00033-00 Therapy module assembly (no pacer) (FRU) 1
801-0652-00034-00 Therapy module assembly (with pacer) (FRU) 1

801-0651-00035-00 Main control module (FRU) 1
0000-10-11158 CF card, 1GB. iCF4000Y 1

801-0651-00009-00 MPM module (without NIBP) 1
801-0651-00012-00 MPM module (Mindray SPO2) 1

801-0651-00013-00 MPM module (Masimo SPO2) 1
801-0651-00014-00 MPM module (Nellcor SPO2) 1

801-0651-00015-00 MPM module (NIBP) 1
801-0651-00016-00 MPM module (NIBP/MindraySPO2) 1
801-0651-00017-00 MPM module (NIBP/MasimoSPO2) 1
801-0651-00018-00 MPM module (NIBP/NellcorSPO2) 1
801-0651-00116-00 12-lead upgrade kit (FRU) 1
801-0651-00119-00 MPM module (without NIBP, FRU) 1
801-0651-00120-00 MPM module (mindray SPO2) 1
801-0651-00033-00 Main control assembly 1
801-0651-00019-00 Parameter interface board assembly (mindraySPO2) 1
801-0651-00020-00 Parameter interface board assembly (masimoSPO2) 1

801-0651-00021-00 Parameter interface board assembly (nellSPO2) 1
8-30

P/N Description Qty
Parameter interface board assembly

801-0651-00084-00 1
(3/5-lead/mindraySPO2)
801-0651-00042-00 M02B watertrap receptacle assembly 1
9201-30-35923 Microstream CO2 connector fixing assembly 1
801-0651-00041-00 Power seat 1
801-0652-00039-00 Pacer function upgrade kit (no overlay) 1

801-0651-00024-00 AC/DC board (FRU) 1
801-0651-00022-00 MPM module Mindray SpO2 board(FRU) 1
801-0651-00088-00 NELLCOR SpO2 board maintenance kit (FRU) 1
0010-10-12275 MASIMO M7 BOARD(MASIMOKIT) 1

801-0651-00002-00 MPM module analog board (Mindray, FRU) 1
801-0651-00003-00 MPM module analog board (Nellcor, FRU) 1

801-0651-00004-00 MPM module analog board (Masimo, FRU) 1
MPM module analog board (Mindray
801-0651-00085-00 1
defibrillator/monitor PCBA, FRU)
801-0651-00023-00 MPM module Masimo adapting board (FRU) 1
801-0651-00001-00 MPM module digital board (lead-free process, FRU) 1

MPM module digital board (lead-free process,
801-0651-00086-00 1
defibrillator monitor PCBA, FRU)
M02B-30-64513 CO2 main unit (M02B module) 1
9201-30-35908 Microstream CO2 adapting board 1
External paddle
801-0651-00006-00 External paddle (Chinese, FRU)

801-0651-00010-00 External paddle (English, FRU)
801-0651-00101-00 External paddle (Spanish, FRU)

801-0651-00102-00 External paddle (German/French/Dutch, FRU)
1
801-0651-00103-00 External paddle (Polish, FRU)
(As configured)
801-0651-00105-00 External paddle (Italian, FRU)
801-0651-00106-00 External paddle (Turkish, FRU)

801-0651-00107-00 External paddle (Russian, FRU)
801-0651-00108-00 External paddle (Brazil Portuguese, FRU)
Miscellaneous
801-0651-00037-00 Paddle tray assembly 1

022-000012-00 Lithium-ion battery, 14.8V, 4500mAh, LI34I001A 2
801-0651-00005-00 Hook mount kit 1
8-31

P/N Description Qty
TR6F-30-67306 TR6F recorder 1

115-008103-00 TR8A recorder (As configured)
0651-20-77032 Test load (MR6901) 1

040-000413-00 Test load (MR6905) 1
040-000099-00 Test load for verification 1
040-000098-00 Test load for calibration 1
801-0651-00007-00 System software package (FRU) 1
8.20.2 Connecting Cables

P/N Description
0651-20-76870 Cable between the CPU board and keypad board
0651-20-76872 Alarm lamp board cable

0651-20-76873 Recorder cable
0651-20-76874 AU LCD cable

0651-20-76875 Cable between the inverter and keypad board (for AU LCD)
0651-20-76878 Cable between the power management board and AC/DC module
0651-20-76886 Sidestream CO2 module connecting cable (M02B)
0651-20-76888 Microstream CO2 module connecting cable
0651-20-76898 Cable between the inverter and keypad board (for Sharp LCD)
0651-20-76871 Cable between MPM module and power management board
0651-20-77133 LCD cable (for Sharp LCD)
0651-20-77134 Inverter cable (for Sharp LCD)
0651-21-76883 Therapy port cable
0651-21-76884 Mode Select knob cable
0651-20-77166 Microstream CO2 connector fixing plate cable (0651)
0651-20-77165 Watertrap cable (0651)

9201-20-35932 Cable between CO2 module and microstream adapter board
009-000484-00 LCD cable (for Toshiba LCD)
8-32

A Electrical Safety Inspection
The following electrical safety tests are recommended as part of a comprehensive preventive
maintenance program. They are a proven means of detecting abnormalities that, if undetected,
could prove dangerous to either the patient or the operator. Additional tests may be required
according to local regulations.
All tests can be performed using commercially available safety analyzer test equipment.
These procedures assume the use of a 601PROXL International Safety Analyzer or equivalent
safety analyzer. Other popular testers complying with IEC 60601-1 used in Europe such as
Fluke, Metron, or Gerb may require modifications to the procedure. Follow the instructions
of the analyzer manufacturer.
The consistent use of a safety analyzer as a routine step in closing a repair or upgrade is
emphasized as a mandatory step if an approved agency status is to be maintained. The safety
analyzer also proves to be an excellent troubleshooting tool to detect abnormalities of line
voltage and grounding, as well as total current loads.
A.1 Power Cord Plug
A.1.1 The Power Plug

Test Item Acceptance Criteria
The power plug pins No broken or bent pin. No discolored pins.

The plug body No physical damage to the plug body.
The power plug No physical damage to the strain relief. No plug
The strain relief
warmth for device in use.
The power plug No loose connections.
No physical damage to the cord. No
deterioration to the cord.
For devices with detachable power cords,
The power cord
inspect the connection at the device.
For devices with non-detachable power cords,
inspect the strain relief at the device.
A-1

A.2 Device Enclosure and Accessories
A.2.1 Visual Inspection

No physical damage to the enclosure and

accessories.
No physical damage to meters, switches,

connectors, etc.
The enclosure and accessories
No residue of fluid spillage (e.g., water, coffee,
chemicals, etc.).
No loose or missing parts (e.g., knobs, dials,

terminals, etc.).
A.2.2 Contextual Inspec tio n

No unusual noises (e.g., a rattle inside the case).

No unusual smells (e.g., burning or smoky
The enclosure and accessories
smells, particularly from ventilation holes).
No taped notes that may suggest device

deficiencies or operator concerns.
A.3 Device Labeling

Check the labels provided by the manufacturer or the healthcare facility are present and
legible.
 Main unit label
 Integrated warning labels
A-2

A.4 Protective Earth Resistance

Protective Earth Resistance is measured using the RED test lead attached to the DUT
Protective Earth terminal or enclosure. Select the test current by pressing SOFT KEY 3 to
toggle between 1AMP, 10AMP, and 25AMP. The front panel outlet power is turned off for
this test.
The following conditions apply: L1 and L2 Open.
Preparation
1. First select the test current that will be used for performing the Protective Earth
Resistance test by pressing AMPERES (SOFT KEY 3).
2. Connect the test lead(s) between the RED input jack and the GREEN input jack.
3. Press CAL LEADS. The 601PRO will measure the lead resistance, and if less than 0.150
Ohms, it will store the reading and subtract it from all earth resistance readings taken at
the calibrated current.
If the calibration fails, the previously stored readings will be used until a passing calibration
has occurred.:
WARNING
 During Earth Resistance testing, the DUT must be plugged into the 601PRO
front outlet. If the DUT fails Earth Resistance, discontinue tests and label the
device defective.
A-3

To Perfo rm the Test

1. From the MAIN MENU, or with the outlet unpowered, plug the DUT into the 601PRO
front panel outlet.
2. Attach the 601PRO RED input lead to the device’s Protective Earth terminal or an
exposed metal area.
3. Press shortcut key 3. The Protective Earth Resistance test is displayed.
4. Press SOFT KEY 3 to select a test current (1AMP, 10AMP, or 25AMP). The selected
test current is displayed in the upper right corner of the display.
5. Press START TEST to start the test. The test current is applied while resistance and
current readings are taken. This takes approximately 5 seconds.
6. Press the print data key at any time to generate a printout of the latest measurement(s).
NOTE
 When "Over" is displayed for Ohms, this signifies that a valid measurement was
not obtained because either an open connection was detected or that the
measurement was not within range. Readings greater than 9.999 Ohms will be
displayed as Over.
In Case of Failure
Once it reaches the limitation, stop using and inform the Customer Service Engineer for
analysis and disposal.
Limits
 R = 0.1Ω Maximum
A-4

A.5 Earth Leakage Test

Run an Earth Leakage test on the device being tested before performing any other leakage
tests.
Leakage current is measured the following ways:
 Earth Leakage Current, leakage current measured through DUT outlet Earth
 Earth Leakage Current AP-EARTH (ALL Applied Parts connected to Earth), leakage
current measured through DUT outlet Earth
There is no need to attach a test lead; the 601PRO automatically connects the measuring
device internally.

front panel outlet, and turn on the device.
2. Attach the device's applied parts to the 601PRO applied part terminals if applicable.
3. Press shortcut key 4.The Earth Leakage test appears on the display, and the test begins
immediately:
 SOFT KEY 1 toggles the DUT outlet Polarity from Normal to Off to Reverse.
 SOFT KEY 2 toggles the DUT outlet from Earth to No Earth.
 SOFT KEY 3 toggles the DUT outlet from L2 to No L2.
 SOFT KEY 4 toggles the AP to Earth to No AP to Earth.
4. Press the print data key at any time to generate a printout of the latest measurement.
A-5

In Case of Failure
 Check any broken of the enclosure. Replace any defective part.
 Inspect wiring for bad crimps, poor connections, or damage.
 Test the wall outlet; verify it is grounded and is free of other wiring abnormalities.
Notify the user or owner to correct any deviations. As a work around, check the other
outlets to see if they could be used instead.
 Change another probe to confirm if the fail is caused by console.
 If the leakage current measurement tests fail on a new unit and if situation can not be
corrected, submit a Safety Failure Report to document the system problem. Remove unit
from operation.
 If all else fails, stop using and inform the Customer Service Engineer for analysis and
disposal.
Limits
 300 μA in Normal Condition
 1000 μA in Single Fault Condition
A.6 Patient Leakage Current

Patient leakage currents are measured between a selected applied part and mains earth. All
measurements may have either a true RMS or a DC-only response.
Preparation
Perform a calibration from the Mains on Applied Part menu.
The following outlet conditions apply when performing this test:
 Normal Polarity, Earth Open, Outlet ON Normal Polarity, Outlet ON
 Normal Polarity, L2 Open, Outlet ON Reversed Polarity, Outlet ON
 Reversed Polarity, Earth Open, Outlet ON Reversed Polarity, L2 Open, Outlet ON
A-6

WARNING
 If all of the applied parts correspond to the instrument type, the applied parts
will be tied together and one reading will be taken. If any of the applied parts
differ from the instrument type, all applied parts will be tested individually,
based on the type of applied part. This applies to Auto and Step modes only.

2. Attach the applied parts to the 601PRO's applied part terminals.
3. Press shortcut key 6. The Patient Leakage test is displayed, and the test begins
immediately.
4. Press APPLIED PART (SOFT KEY 4) at any time to select the desired applied part
leakage current.
5. Modify the configuration of the front panel outlet by pressing the appropriate SOFT
KEY on the 601PRO.
NOTE
 If the current test standard being used does not include Patient Leakage DC
readings, or the DC option is not enabled, then DC readings will not be available
through the APPLIED PART SOFT KEY selections. Refer to Chapter 8,
Standards and Principles.
 For external or internal paddle, the patient leakage current test should be tested
when the EUT was charging.
A-7

In Case of Failure
from operation.
disposal.
Limits
 For ECG (Defibrillator proof) and other CF applied parts
 10 μA in Normal Condition
 50 μA in Single Fault Condition
 For BF applied parts
 10 μA DC,100μA AC in Normal Condition
 50 μA DC,500μA AC in Single Fault Condition
A-8

A.7 Mains on Applied Part Leakage

The Mains on Applied Part test applies a test voltage, which is 110% of the mains voltage,
through a limiting resistance, to selected applied part terminals. Current measurements are
then taken between the selected applied part and earth. Measurements are taken with the
test voltage (110% of mains) to applied parts in the normal and reverse polarity conditions as
indicated on the display.
The following outlet conditions apply when performing the Mains on Applied Part test.
 Normal Polarity;
 Reversed Polarity
Preparation
To perform a calibration from the Mains on Applied Part test, press CAL (SOFT KEY 2).
1. Disconnect ALL patient leads, test leads, and DUT outlet connections.
2. Press CAL to begin calibration, as shown:
If the calibration fails, the previously stored readings will be used until a passing
calibration has occurred. Also, the esc/stop key has no effect during calibration.
3. When the calibration is finished, the Mains on Applied Part test will reappear.
WARNING
 A 2-beep-per-second signal indicates high voltage present at the applied part
terminals while a calibration is being performed.
 High voltage is present at applied part terminals while measurements are being
taken.
A-9


1. From the MAIN MENU, or with the outlet unpowered, plug the DUT into the 601
2. Attach the applied parts to the 601PRO applied part terminals.
3. Attach the red terminal lead to a conductive part on the DUT enclosure.
4/ Press shortcut key 7. The Mains on Applied Part test is displayed.
5. Select the desired outlet configuration and applied part to test using the appropriate
SOFT KEYS:
6. Press START TEST (SOFT KEY 1) to begin the test.
7. Press the print data key to generate a printout of the latest measurement.
NOTE
 If all of the applied parts correspond to the instrument type, the applied parts
will be tied together and one reading will be taken. If any of the applied parts
differ from the instrument type, all applied parts will be tested individually,
based on the type of applied part. This applies to Auto and Step modes only.
In Case of Failure
from operation.
disposal.
A-10

Limits
 For ECG (Defibrillator proof) and other CF applied parts
 50 μA
 5000 μA
A.8 Patient Auxiliary Current

Patient Auxiliary currents are measured between any selected ECG jack and the remaining
selected ECG jacks. All measurements may have either a true RMS or a DC-only response.
Preparation
2. Attach the patient leads to the 601PRO ECG jacks.
3. Define the Lead Types from the View Settings Option (refer to: Lead Type Definitions
in Section 5 of this chapter).
4. Press shortcut key 8. The Patient Auxiliary Current test is displayed, and the test begins
immediately. Display values are continuously updated until another test is selected.
5. Press SOFT KEYS 1-4 to select leakage tests
6. Press APPLIED PART (SOFT KEY 4) at any time to select the desired applied part
leakage current:
7. Modify the configuration of the front panel outlet by pressing the appropriate SOFT
KEY on the 601PRO:
A-11

NOTE
 If the current test standard being used does not include Patient Auxiliary
Current DC readings, or the DC option is not enabled, then DC readings will not
be available through the APPLIED PART SOFT KEY selections.
 For external or internal paddle, the patient auxiliary current test should be
tested when the EUT was charging.
In Case of Failure
from operation.
disposal.
Limits
 For ECG (defibrillator proof) and other CF applied parts
 10μA in Normal Condition
 50μA in Single Fault Condition
 10μA DC,100μA AC in Normal Condition
 50μA DC,500μA AC in Single Fault Condition
A.9 Functional test

For functional test items, please refer to relevant functional tests in Chapter4 Testing and
Maintenance.
A-12

ELECTRICAL SAFETY INSPECTION FORM
Overall assessment:
 Scheduled inspection: Test item 1, 2, 3, 9
 Unopened repair type: Test item 1, 2, 3, 9
 Opened repair type, not modify the power board and patient circuit board: Test item 1, 2,
3, 4, 5, 9
 Opened repair type, modify the power board or patient circuit board: Test item 1, 2, 3, 4,
5, 6, 7, 8, 9
Location: Technician:
Equipment: Control Number:
Manufacturer: Model: SN:
Measurement equipment /SN Date of Calibration:
INSPECTION AND TESTING Pass/Fail Comments
1 Power Cord Plug
2 Device Enclosure and Accessories
3 Device Labelling
4 Protective Earth Resistance _____ Ω Max 0.1 Ω
5 EARTH Normal condition(NC) ____ μA Max
Leakage Single Fault ____ μA NC:500μA,
condition(SFC) SFC:1000μA
6* Patient Normal condition(NC) ____ μA Max
Leakage Single Fault ____ μA CF AP
Current condition(SFC) NC:10μA, SFC: 50μA
BF AP
NC:100μA, SFC: 500μA
7* Mains on Applied Part Leakage Max
CF AP: 50μA
BF AP: 5000μA
8* Patient Normal condition(NC) ____ μA Max
Auxiliary Single Fault ____ μA CF AP
Current condition(SFC) NC:10μA, SFC: 50μA
BF AP
NC:100μA, SFC: 500μA
9 Functional test (parameters tested):
Note: The test items marked “*” are needed only for incoming inspections and after repairs or
modifications that may have affected lead leakage [NFPA 99 (2005)8.5.2.1.3].
Deficiency / Note:
Name/Signature: _________________________ Date: ________________________
A-13

FOR YOUR NOTES
A-14

P/N: 0651-20-77084 (8.0)

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Intellectual Property Statement

, , and are the registered trademarks or

 Version number 7.0

 Release time: May 2011

E-mail Address: service@mindray.com

Tel: +86 755 26582479, +86 755 26582888

Fax: +86 755 26582934, +86 755 26582500

 Installation mode: 888888

 Service mode: 332888

 Configuration mode: 315666

2 Theory of Operation ........................................................................................................ 2-1

3 Unpacking and Installation ............................................................................................. 3-1

4 Testing and Maintenance................................................................................................. 4-1

4.2.1 Visual Test .......................................................................................................... 4-4

5 Hardware and Software Upgrade................................................................................... 5-1

6 Troubleshooting ................................................................................................................ 6-1

6.1 Overview......................................................................................................................... 6-1

7 Disassembly and Repair .................................................................................................. 7-1

7.4.3 Removing the Speaker ..................................................................................... 7-20

8 Parts .................................................................................................................................. 8-1

8.6 Measurement Module Panel Assembly ......................................................................... 8-12

8.20.2 Connecting Cables ......................................................................................... 8-32

 The equipment must be connected to a properly installed power socket with

 Refer to Operation Manual for detailed operation and other information.

1.2 Equip ment Symbols

Attention: Please read this

Danger: High-voltage Service indicator

Alternating current(AC) Network connector

Battery Video output

USB connector Analog input/out

ESD warning symbol for Electrostatic sensitive devices.

Type CF applied part. Defibrillator-proof protection against electric shock.

Type BF applied part. Defibrillator-proof protection against electric shock.

FOR YOUR NOTES

2.1.2 Main Functions

 Manual Defib Mode

3 Deliver the shock.

Defibrillation may be performed through external paddles or multifunction electrode pads. In

In Monitor Mode, the equipment is intended for monitoring, displaying, reviewing,

The main unit is the core of the equipment. It provides:

 Overall system control;

 System power supply;

 Defibrillation and pacing;

 Audible and visible alarms;

 Multiple parameter measurements;

 External connectors and communication; and

 Recording, printing and data storage.

2.3 Main Unit

 The paddle tray is for holding the external paddles.

The main unit consists of the following subsystem:

 Power management subsystem: includes batteries, AC/DC board and power

 External device connection subsystem: includes USB connector, network connector,

System Signal Flow

2.4 Front Housing Assembly

Mode Select Knob

Power Interface Introduces DC power supply from the CPU board.

Al arm Lamp B oar d