Mindray BeneView T6, BeneView T8, BeneView T9 User guide

BeneView T6/T8/T9

Patient 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.

Mindray intends to maintain the contents of this manual as confidential information.

Disclosure of the information in this manual in any manner whatsoever without the written

permission of Mindray is strictly forbidden. Release, amendment, reproduction, distribution,

rent, adaption and translation of this manual in any manner whatsoever without the written

permission of Mindray is strictly forbidden.

, , and are the registered trademarks or

trademarks owned by Mindray in China and other countries. All other trademarks that appear

in this manual are used only for editorial purposes without the intention of improperly using

them. They are the property of their respective owners.

Contents of this manual are subject to changes without prior notice.

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.

 Revision number: 13.0
 Release time: April, 2016

© 2006-2016 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.

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.

This manual is based on the maximum configuration; Therefore, some contents may not

apply to your monitor. If you have any question, please contact our Customer Service

Department.

Intended Audience

This manual is for biomedical engineers, authorized technicians or service representatives

responsible for troubleshooting, repairing and maintaining the patient monitors.

II

Abbreviations

Abbreviations used in this manual are:

MPM multi-parameter module

SMR satellite module rack

CMS central monitoring system

PCB printed circuit board

Passwords

A password may be required to access different modes within the monitor. The passwords are

listed below:

 User maintenance: 888888 (User adjustable)
 Factory maintenance: 332888
 Demo mode: 2088
 Configuration mode: 315666 (User adjustable)
 iView login: MINDRAY

NOTE

z When log in iView system and input the password, connect the keyboard to the

special USB connector for iView system.

III

FOR YOUR NOTES

IV

Contents

1 Safety................................................................................................................................. 1-1

1.1 Safety Information ..........................................................................................................1-1

1.1.1 DANGER ........................................................................................................... 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 Introduction..................................................................................................................... 2-1

2.2 System Connections........................................................................................................ 2-2

2.2.1 Mounting the Patient Monitor............................................................................ 2-2

2.2.2 Connectors for Peripheral Devices..................................................................... 2-3

2.3 Main Unit ........................................................................................................................ 2-4

2.3.1 Input System ...................................................................................................... 2-5

2.3.2 Output System.................................................................................................... 2-6

2.3.3 Processing and Communications System........................................................... 2-7

2.3.4 Power Management System............................................................................... 2-9

2.3.5 Equipment Interface System ............................................................................ 2-13

2.4 Parameter Module ......................................................................................................... 2-15

2.4.1 Module Infrared Communication Board .......................................................... 2-15

2.4.2 Module Power Board ....................................................................................... 2-15

2.4.3 Parameter Board............................................................................................... 2-15

2.5 Satellite Module Rack................................................................................................... 2-16

2.6 BeneLink Module.......................................................................................................... 2-17

3 Testing and Maintenance................................................................................................. 3-1

3.1 Introduction..................................................................................................................... 3-1

3.1.1 Test Equipment................................................................................................... 3-1

3.1.2 Test Report ......................................................................................................... 3-1

3.1.3 Preventative Maintenance .................................................................................. 3-2

3.1.4 Recommended Frequency.................................................................................. 3-2

3.2 Preventative Maintenance Procedures ............................................................................ 3-4

3.2.1 Visual Inspection ................................................................................................ 3-4

3.2.2 NIBP Tests.......................................................................................................... 3-5

3.2.3 Sidestream and Microstream CO

3.2.4 AG Tests........................................................................................................... 3-10

3.2.5 Preventative maintenance test report................................................................ 3-14

3.3 Power On Test ............................................................................................................... 3-16

3.4 Module Performance Tests ............................................................................................ 3-16

Module Tests................................................ 3-7

2

1

3.4.1 ECG Tests......................................................................................................... 3-16

3.4.2 Resp Performance Test..................................................................................... 3-17

3.4.3 SpO

Test.......................................................................................................... 3-18

2

3.4.4 NIBP Tests........................................................................................................ 3-18

3.4.5 Temp Test......................................................................................................... 3-18

3.4.6 IBP Tests........................................................................................................... 3-19

3.4.7 C.O. Test........................................................................................................... 3-21

3.4.8 Mainstream CO

3.4.9 Sidestream and Microstream CO

Tests...................................................................................... 3-21

2

Module Tests.............................................. 3-23

2

3.4.10 AG Tests......................................................................................................... 3-23

3.4.11 ICG Test ......................................................................................................... 3-23

3.4.12 BIS Test.......................................................................................................... 3-24

3.4.13 RM Test.......................................................................................................... 3-25

3.4.14 CCO/SvO

Tests ............................................................................................. 3-26

2

3.4.15 PiCCO Tests ................................................................................................... 3-27

3.4.16 ScvO

Tests .................................................................................................... 3-30

2

3.4.17 NMT Tests ...................................................................................................... 3-31

3.4.18 EEG tests........................................................................................................ 3-33

3.5 Nurse Call Relay Performance Test .............................................................................. 3-34

3.6 Analog Output Performance Test .................................................................................. 3-34

3.7 Electrical Safety Test..................................................................................................... 3-34

3.8 Touchscreen Calibration................................................................................................ 3-35

3.9 Recorder Check............................................................................................................. 3-35

3.10 Network Print Test ...................................................................................................... 3-35

3.10.1 Equipment Connection and Setup.................................................................. 3-36

3.10.2 Print Function Test ......................................................................................... 3-36

3.11 BeneLink Module Check............................................................................................. 3-37

3.11.1 Device Connection and Setup ........................................................................ 3-37

3.11.2 Device Integration Function Test ................................................................... 3-39

3.11.3 Installation and Test Report............................................................................ 3-43

3.12 Battery Check.............................................................................................................. 3-44

3.13 iView System Maintenance(for T8 and T9 monitors only) ......................................... 3-45

3.13.1 Making USB Startup Disk.............................................................................. 3-45

3.13.2 Restoring the System...................................................................................... 3-47

3.13.3 Setting Automatic Login ................................................................................ 3-53

3.14 Factory Maintenance................................................................................................... 3-54

3.14.1 Accessing Factory Maintenance Menu........................................................... 3-54

3.14.2 Drawing Waves .............................................................................................. 3-54

3.14.3 Recorder ......................................................................................................... 3-54

3.14.4 Software Version ............................................................................................ 3-55

3.14.5 Monitor Information....................................................................................... 3-55

4 Troubleshooting................................................................................................................ 4-1

4.1 Introduction..................................................................................................................... 4-1

2

4.2 Part Replacement ............................................................................................................4-1

4.3 Patient Monitor Status Check.......................................................................................... 4-1

4.4 Software Version Check .................................................................................................. 4-2

4.5 Technical Alarm Check ................................................................................................... 4-2

4.6 Troubleshooting Guide.................................................................................................... 4-2

4.6.1 Power On/Off Failures ....................................................................................... 4-2

4.6.2 Display Failures ................................................................................................. 4-3

4.6.3 Module Rack Failures ........................................................................................ 4-4

4.6.4 Alarm Problems.................................................................................................. 4-6

4.6.5 Button and Knob Failures .................................................................................. 4-7

4.6.6 Recorder Failures ............................................................................................... 4-7

4.6.7 Interface Failures................................................................................................ 4-8

4.6.8 CF Card Problems.............................................................................................. 4-9

4.6.9 Power Supply Failures ....................................................................................... 4-9

4.6.10 Network Related Problems..............................................................................4-11

4.6.11 Software Upgrade Problems........................................................................... 4-12

4.6.12 Technical Alarm Messages............................................................................. 4-12

4.6.13 M51A Self Test Information........................................................................... 4-12

4.6.14 Device Integration Failures ............................................................................ 4-13

5 Repair and Disassembly .................................................................................................. 5-1

5.1 Tools................................................................................................................................ 5-1

5.2 Preparations for Disassembly.......................................................................................... 5-1

5.3 Basic Disassembly .......................................................................................................... 5-2

5.3.1 Disconnecting the Base ...................................................................................... 5-2

5.3.2 Separating the Front and Rear Half of the Monitor............................................ 5-4

5.4 Further Disassembly........................................................................................................ 5-7

5.4.1 Removing the Power Switch & LED Board ...................................................... 5-7

5.4.2 Disconnecting the Encoder Assembly................................................................ 5-8

5.4.3 Removing the Button Board............................................................................... 5-8

5.4.4 Removing the Touchscreen Control Board ........................................................ 5-9

5.4.5 Removing the Inverter of T6 and T8................................................................ 5-10

5.4.6 Removing the Backlight Board of T9 ...............................................................5-11

5.4.7 Removing the LCD Screen .............................................................................. 5-12

5.4.8 Removing the Alarm Lamp Board ................................................................... 5-14

5.4.9 Removing the Wireless AP............................................................................... 5-15

5.4.10 Removing the CF Assembly........................................................................... 5-17

5.4.11 Removing the Main Board ............................................................................. 5-18

5.4.12 Removing the Fan .......................................................................................... 5-20

5.4.13 Removing the Speaker ................................................................................... 5-20

5.4.14 Removing the Interface Board Assembly....................................................... 5-21

5.4.15 Removing the iView Assembly (for T8 and T9 monitor only)....................... 5-22

5.4.16 Removing the Power Supply Assembly ......................................................... 5-25

5.4.17 Removing the Integral Module Rack ............................................................. 5-28

3

5.4.18 Removing the Recorder.................................................................................. 5-33

5.5 Removing the SMR Assembly ...................................................................................... 5-38

5.6 Disassembling Modules ................................................................................................ 5-42

5.6.1 Disassembling the ICG Module ....................................................................... 5-42

5.6.2 Disassembling CO

Module ............................................................................. 5-46

2

5.6.3 Disassembling the BeneLink Module .............................................................. 5-52

5.6.4 Disassembling the New MPM Module ............................................................ 5-55

6 Parts .................................................................................................................................. 6-1

6.1 Introduction..................................................................................................................... 6-1

6.2 Main Unit (T6/T8）........................................................................................................ 6-2

6.3 Main Unit (T9)................................................................................................................ 6-3

6.4 Base Assembly ................................................................................................................ 6-4

6.5 Front housing Assembly.................................................................................................. 6-5

6.5.1 17” LCD with Anti-glare Screen ........................................................................ 6-5

6.5.2 15” LCD with Anti-glare Screen ........................................................................ 6-7

6.5.3 19” LCD Touchscreen........................................................................................ 6-9

6.5.4 17” LCD Touchscreen.......................................................................................6-11

6.5.5 15” LCD Touchscreen...................................................................................... 6-13

6.6 Rear Housing Assembly................................................................................................ 6-15

6.6.1 Rear Housing Assembly................................................................................... 6-15

6.6.2 Power module................................................................................................... 6-17

6.6.3 Integral Module Rack....................................................................................... 6-18

6.6.4 Interface Board Assembly ................................................................................ 6-19

6.6.5 Main Support Assembly (T8/T9) ..................................................................... 6-21

6.6.6 Main Support Assembly (T6)........................................................................... 6-22

6.6.7 Main Control Board Assembly......................................................................... 6-23

6.6.8 6800 Wireless AP Kit (ASUS) ......................................................................... 6-24

6.6.9 Others ............................................................................................................... 6-25

6.7 SMR Assembly ............................................................................................................. 6-26

6.7.1 SMR Assembly................................................................................................. 6-26

6.7.2 SMR Inside Assembly...................................................................................... 6-28

6.8 Parameter Modules........................................................................................................ 6-29

6.8.1 MPM Module................................................................................................... 6-29

6.8.2 New MPM Module .......................................................................................... 6-31

6.9 Remote Display Box ..................................................................................................... 6-33

6.10 New Wireless AP Package for 6800/6802................................................................... 6-35

6.11 Replaceable Parts ........................................................................................................ 6-36

6.11.1 Main Unit ....................................................................................................... 6-36

6.11.2 SMR ............................................................................................................... 6-38

6.11.3 Parameter Modules......................................................................................... 6-39

6.11.4 Cables............................................................................................................. 6-40

7 Upgrade............................................................................................................................. 7-1

4

7.1 Introduction..................................................................................................................... 7-1

7.2 Upgrading Parameter Modules........................................................................................ 7-2

7.3 Upgrading Functional Assemblies .................................................................................. 7-4

7.3.1 Upgrading SMR ................................................................................................. 7-4

7.3.2 Upgrading Wireless Network Function.............................................................. 7-4

7.3.3 Upgrading Recorder ........................................................................................... 7-5

7.3.4 Upgrading Analog Output.................................................................................. 7-5

7.3.5 Upgrading iView System ................................................................................... 7-5

7.4 Upgrading Software ........................................................................................................ 7-6

7.4.1 How to Upgrade Software.................................................................................. 7-8

A Electrical Safety Inspection ........................................................................................... A-1

A.1 Power Cord Plug ........................................................................................................... A-1

A.2 Device Enclosure and Accessories................................................................................ A-2

A.2.1 Visual Inspection .............................................................................................. A-2

A.2.2 Contextual Inspection....................................................................................... A-2

A.3 Device Labeling ............................................................................................................ A-2

A.4 Protective Earth Resistance........................................................................................... A-2

A.5 Earth Leakage Test ........................................................................................................ A-4

A.6 Patient Leakage Current................................................................................................ A-6

A.7 Mains on Applied Part Leakage .................................................................................... A-7

A.8 Patient Auxiliary Current .............................................................................................. A-9

A.9 Scheduled Electrical Safety Inspection ........................................................................A-11

A.10 Electrical Safety Inspection after Repair................................................................... A-12

5

FOR YOUR NOTES

6

1 Safety

1.1 Safety Information

DANGER

z Indicates an imminent hazard that, if not avoided, will result in death or serious

injury.

WARNING

z Indicates a potential hazard or unsafe practice that, if not avoided, could result in

death or serious injury.

CAUTION

z Indicates a potential hazard or unsafe practice that, if not avoided, could result in

minor personal injury or product/property damage.

NOTE

z Provides application tips or other useful information to ensure that you get the

most from your product.

1-1

1.1.1 DANGER

There are no dangers that refer to the product in general. Specific “Danger” statements may

be given in the respective sections of this manual.

1.1.2 Warnings

WARNING

z All installation operations, expansions, changes, modifications and repairs of this

product are conducted by Mindray authorized personnel.

z There is high voltage inside the equipment. Never disassemble the equipment

before it is disconnected from the AC power source.

z When you disassemble/reassemble a parameter module, a patient leakage current

test must be performed before it is used again for monitoring.

z The equipment must be connected to a properly installed power outlet with

protective earth contacts only. If the installation does not provide for a protective

earth conductor, disconnect it from the power line and operate it on battery power,

if possible.

z Dispose of the package material, observing the applicable waste control regulations

and keeping it out of children’s reach.

1.1.3 Cautions

CAUTION

z 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.

z 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.

z Protect the equipment from damage caused by drop, impact, strong vibration or

other mechanical force during servicing.

1-2

1.1.4 Notes

NOTE

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

1.2 Equipment Symbols

Attention: Consult

accompanying documents

(this manual).

iView network connector

Danger: High-voltage

Alternating current(AC)

Power ON/OFF

Battery indication

Zero key

Calibrate key

Measure/Standby

Check sensor

ESD warning symbol for Electrostatic sensitive devices.

Network connector

Defibrillator connector

Connector for satellite

module rack

Video output

Auxiliary output connector

USB connector

Equipotential terminal

CE marking

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 Introduction

This patient monitor is designed to monitor a fixed set of physiological parameters including

ECG, heart rate (HR), respiration (Resp), temperature (Temp), SpO

non-invasive blood pressure (NIBP), invasive blood pressure (IBP), cardiac output (C.O.),

carbon dioxide (CO

bispectral index (BIS), respiration mechanics (RM), continuous cardiac output (PiCCO),

central venous oxygen saturation (ScvO

transmission (NMT).

), oxygen (O2), anesthetic gas (AG), impedance cardiograph (ICG),

2

), electroencephalograph (EEG), and neuromuscular

2

, pulse rate (PR),

2

The patient monitor also:

 Provides audible and visual alarm indications in case of patient or equipment problems.
 Enables displaying, reviewing, storing and transferring of real-time data.
 Incorporates multiple input devices such as buttons, knob, touchscreen, keyboard and

mouse.

 Interfaces a clinical information system or central monitoring system.
 Enables program upgrade over the network.
 Integrates the information of other devices, which include but are not restricted to

anesthesia machine and ventilator.

2-1

2.2 System Connections

2.2.1 Mounting the Patient Monitor

The patient monitor can be mounted on a wall bracket or on a trolley support. The wall

bracket or trolley support can be ordered optionally. Each type of mounting bracket is

delivered with a complete set of mounting hardware and instructions. Refer to the

documentation delivered with the mounting hardware for instructions on assembling mounts.

CAUTION

z Use mounting brackets we supply or approve. If other compatible mounting

bracket is used, be sure it can be safely used on the patient monitor.

z The mounting bracket should be installed by our qualified service personnel, or

engineers who have adequate knowledge on it.

z If other mounting solution is used, the installation personnel and the customer

should verify if it can be safely used on the patient monitor, and the customer

assume the responsibility for any risk resulting from that.

2-2

2.2.2 Connectors for Peripheral Devices

On the back of the patient monitor you will find all connectors for peripheral devices.

1. AC Power Connector: used to connect an AC power source (100 to 240 VAC, 50/60Hz).

2. Equipotential Terminal: used to connect the equipotential terminal of other equipment,

eliminating potential difference between different pieces of equipment.

3. SMR Connector: It outputs a 12V DC, used to connect the SMR.

4. Video Output: It is a DVI-D connector used to connect a secondary display.

5. iView Network Connector: It is a RJ45 connector that connects iView system to external

network.

6. Network Connector: It is a RJ45 connector used to connect an ethernet network or a PC.

7. Analog Output and Defibrillator Connector: It is a Micro-D connector used to output

analog signals and defibrillator synchronization signals.

8. Auxi Output Connector: It is a BNC connector used to output nurse call signals.

9. Secondary USB Connector: used to connect the mouse and keyboard of the secondary

display.

10. Special USB Connectors: used for iView maintenance and data transfer.

11. General USB Connector: used to connect any USB-compatible peripheral device.

2-3

2.3 Main Unit

The patient monitor consists of:

 Input system: button board, knob, touchscreen, power switch and LED board
 Output system: LCD panel, alarm LED board, recorder, speaker
 Processing and communications system: main board, iView assembly, integral module

rack

 Power management system: battery, battery interface board, power module
 Equipment interface system: USB interface board, DVI interface board, CF card

assembly and internal wireless network card.

Additionally, the patient monitor can also connect satellite module rack (SMR), parameter

modules, BeneLink module, mouse, keyboard, etc.

The following diagram illustrates the structure of the patient monitor.

2-4

2.3.1 Input System

Button board

The button board, located at the lower part of the monitor’s front panel, contains 6 keys and

provides connections for the following components to the main board:

 Knob
 Power switch & LED board
 Touchscreen control board
 Backlight board/Inverter
 Alarm LED board

The following diagram shows the button board connections.

Knob

The knob can be pressed, or rotated both clockwise and counter-clockwise. It is connected

with the button board.

Touchscreen

The touchscreen enables touch operations and can be calibrated. It is connected with the

touchscreen control board and main board.

Power switch & LED Board

The power switch & LED board controls the power supply for the main unit. It has three

LEDs, which respectively indicate the AC power status, battery status and monitor power

on/off status. It is connected with the button board.

2-5

2.3.2 Output System

LCD

The patient monitor adopts a high-resolution LCD. The LCD is connected with the main

board. Signals and power supply of the backlight board are transferred by the button board.

Alarm Lamp

The patient monitor has two alarm lamps: alarm lamp and technical alarm lamp. Alarm lamp

lights either red or yellow whereas technical alarm lamp lights blue only. The signals from

the alarm lamps are transferred by the button board and are controlled directly by the main

board.

Recorder

The recorder receives data coming form the main board and then sends them to the thermal

printhead for printing. The recorder has a hardkey (starting/stopping recordings) and a green

LED on its front. It is connected with the main board.

The following diagram shows its operating principle.

2-6

Module Description

Power interface Introduces a DC from the main board.

Power module

CPU Control the communications between modules.

Signal interface

Motor drive circuit

Button & LED

board

Converts the input power into voltages that fit each module and then

forwards them to each module.

Control the communications between the main board and the

recorder CPU.

Receives the control signals from the CPU and then forwards them to

the step engines.

Includes one button and one LED which are directly controlled by

the CPU.

Speaker

The speaker provides sound for alarms, key strokes, heart beats and pulse, and allows PITCH

TONE and multi-level tone modulation. It is connected with the main board and is directly

driven by the main board.

2.3.3 Processing and Communications System

Main Board

The main board is the heart of the patient monitor. It implements a series of tasks including

input & output control, data storage and processing, display processing, system control,

communication management, printing management and alarming, etc.

The main board comprises the CPU board and mother board. The following diagram shows

interfaces to other components.

2-7

The CPU board is an essential CPU system containing the CPU, FLASH, memory, realtime

clock, EEPROM, etc. It interfaces to the mother board only, which then provides interfaces to

all other external devices.

The mother board is in charge of connections and communications with other components

and provides the following interfaces:

 LCD port: connects a built-in display.
 Video output+network+IO+IIC: connects the digital video interface board.
 USB×2+UART: connects the USB interface board.
 Button board port: connects the button board.
 Integral module rack port: connects integral module rack communication board.
 Fan port: connects the fan.

2-8

 Speaker port: connects the speaker.
 Power module port: connects the power module.
 iView port: located at the back of the mother board for connecting the iView

components.

 CF port: connects the CF card assembly.
 Recorder port: connects the recorder.
 Internal wireless network card port: connects the internal wireless network card

iView System

iView sytem includes iView mother board, computer board, hard disk and so on. iView

system connects to main control board, DVI interface board and USB interface board. The

iView system transmits the network signal to host network interface through DVI interface

board.

Integral Module Rack

The patient monitor has two kinds of integral module rack: 2-slot and 5-slot. The control

board includes a NIOS II FPGA. It implements protocol conversion and infrared

communication between the main unit and the parameter modules.

The module rack communication board can be a 2-slot type or a 3-slot type. The 3-slot

communication board communicates the main board directly. The 2-slot communication

board is connected with and is controlled by the 3-slot communication board. The 3-slot

communication board has the function of communication control. The 2-slot communication

board consists of the infrared circuit and module power circuit. The RS422 drive circuit is

located on the 3-slot communication board.

2.3.4 Power Management System

Battery

The patient monitor uses two chargeable lithium-ion batteries (11.1 V, 4500 mAh). The

battery compartment door is located at the bottom of the patient monitor. The battery power

is introduced to the power module via the battery interface board, and then processed and

distributed to each component by the power module.

NOTE

z Two batteries must be used simultaneously when the patient monitor operates on

battery power. Otherwise, it may cause power supply protection.

2-9

Battery Interface Board

The battery interface board connects batteries to the power module, enabling charging and

discharging between the batteries and the power board.

Power Module

The power module is located at the back of the patient monitor. The main part of the power

module is the power board, which contains 4 PCBs: charging & power management board,

voltage drop DC inverter, voltage rise and drop DC inverter, and voltage drop 5 V CIS power

board.

The power module transforms the input power into DC and then forwards them to each

component of the patient monitor. The input power comes from either the batteries or an AC

source. The patient monitor will run power from the AC source whenever an AC source is

available. If the AC source becomes unavailable, the patient monitor will automatically

switch to the battery power. This does not affect the monitor’s operating status.

Power module has an AC input socket at its backside, and a socket at its front provides 4

connections to the batteries, main board, iView components and USB interface board

respectively. The power module protects itself and the patient monitor by switching off AC

input or DC output in case of overcurrent, short circuit and overvoltage.The power module

provides 4 DC outputs:

Outputs Description

+3.3 V

+5.0 V

+5.0 V CIS Goes to the iView assembly.

+12 V

The systematic principle diagram of the power module is as follows:

Goes to the LCD, mother board, CPU board, DVI interface board and

integral module rack.

Goes to the DVI interface board, recorder, CF storage card board and

USB interface board.

Goes to the recorder, LCD inverter, integral module rack, parameter

modules and USB interface board.

2-10

The following diagram shows the pins of the power module socket (excluding the pins of the

battery power socket. On power board, pin 1 has a triangle symbol):

Pin ID Marking Description Cable

color

2, 4, 6, 7,

13, 15, 17

8 RXD Receives serial communications (the main board sends). Purple

9 TXD Sends serial communications (the main board receives). Brown

10 PCON

11 LCD-EN

GND The output grounding terminal of the power board. Black

Power on/off control signal. It is a TTL pulse signal

inputted from the back board. Every time when the power

on/off switch is pressed (pulse of falling edge), a switch

between power “on” and “off” happens. The pulse

duration is no less than 0.1 s for power-on and no less

than 2 s for power off.

Backlight on/off control signal. The main board sends a

backlight on/off control signal to the power board through

the serial interface. The power board processes the

received signal and then outputs a high or low level

depending on the received signal.

Blue

Green

2-11

Pin ID Marking Description Cable

color

12, 1 12 V

14, 3 5 V CIS

16, 5 5 V

18, 19 3.3 V

20 LED- AC AC power status indication signal White

21 LED- BAT Battery status indication signal. Grey

22 LCD-BR Backlight brightness control voltage. Brown

The positive end of the 12 V DC coming from the power

board.

The positive end of the 5 V CIS coming from the power

board.

The positive end of the 5 V DC coming from the power

board.

The positive end of the 3.3 V DC coming from the power

board.

Yellow

Purple

Red

Orange

2-12

2.3.5 Equipment Interface System

USB Interface Board

The USB interface board is compatible with such USB interfaces as USB2.0, USB1.1 and

USB1.0. It is connected with the main board and the power module. It receives USB

differential signals coming from the main board and then distributes them to maximumly six

USB interfaces via two ISP1521 chips. The USB interface board of iView system directly

connects to two USB interfaces (on USB board) of host. The UART signal output by the

main board is converted into RS422 signal by the USB interface board. The USB interface

board receives 5 VDC and 12 VDC inputs from the power module, of which the 5 VDC goes

to the USB interface board and the 12 VDC outputted to the SMR connector through a fuse.

2-13

DVI Interface Board

The DVI interface board is connected with the mother board and the iView mother board.

The following diagram shows its interfaces to other components.

Interface Description

iView Connector Connects the iView mother board.

BNC connector Outputs nurse call signals.

Micro-D connector Outputs analog signals and defibrillator synchronization signals.

RJ 45 connector

(network)

RJ 45 connector

(iView)

DVI-D connector Connects a secondary display.

It is a standard RJ45 connector, providing 10/100 BASE-TX Ethernet

communications channels. It connects an Ethernet network or a PC.

It is a standard RJ45 connector for connecting a iView network.

CF Card assembly

The CF assembly serves the non-volatile CF storage card which is used for data storage and

transfer. It is connected with the mother board.

Internal wireless network card

The internal wireless network card connects with the mother board. User can set network

type as LAN or WLAN through user interface and can set the internal wireless network card

through PC.

2-14

2.4 Parameter Module

Each parameter module consists of the module infrared communication board, module power

board, module button board, parameter board, etc.

2.4.1 Module Infrared Communication Board

The module infrared communication board allows a short delay when powering up the

module and adopts FPGA to enable infrared communications between the module and the

module rack. An ID is integrated into the module infrared communication board. When a

module is inserted in the module rack, the ID is automatically sent to the module rack.

2.4.2 Module Power Board

Some modules have no power board. There are two kinds of module power board:

1. Isolated power board: converts the 12 V DC into a 12 V isolated DC and a 5 V isolated

DC.

2. Non-isolated power board: converts the 12 V DC into a 5 V DC.

2.4.3 Parameter Board

The parameter board is a parameter measurement component, which is the most important

component of the parameter module.

2-15

2.5 Satellite Module Rack

The satellite module rack (SMR) is independent of the patient monitor, provides 8 slots for

mounting parameter modules. It has the following features:

 It allows a parameter module to be plugged and unplugged with the patient monitor on.

This allows function extension and patient transfer.

 It does not have its own power. It introduces 12 V DC from the patient monitor and then

supplies power to each parameter module via the contact screw.

 It accomplishes communications protocol conversions between the patient monitor and

each parameter module, provides infrared communications for parameter modules, and

is responsible for detecting infrared communications malfunction for each parameter

module.

The following diagram shows the structure of the SMR.

2-16

2.6 BeneLink Module

BeneLink module allows the information (patient data, alarms, etc.) from the external device

to be displayed, saved, recorded, printed, or calculated through a BeneView patient monitor.

If the patient monitor is connected with the CMS or gateway, information from the external

device can also be transmitted to the CMS or gateway. BeneLink module connects with the

external device through an ID module, which enables the information transmission between

the BeneLink module and the external device. BeneLink module can be connected to many

external devices such as anesthesia machine and ventilator.

The following diagram shows the structure of the BeneLink module:

BeneLink module interface
board for debugging

BeneView

patient monitor

External device

Infrared ray

232 Serial port

Infrared

commun

-ication
board

Isolation

circuit

I2S

BeneLink module interface board

Serial port ID interface board

Serial port of external

device

Connector

MCU

Debugging

AM1808

module

CPU

MCU serial

port

serial port

Multiplex switch

VCC

Serial port

ID_READ

ID_STATUS

Up serial port

ID_READ

ID_STATUS

Connector 4

Connector 1

232 Serial port

Connector

2-17

FOR YOUR NOTES

2-18

3 Testing and Maintenance

3.1 Introduction

To ensure the patient monitor always functions normally, qualified service personnel should

perform regular inspection, maintenance and test. This chapter provides a checklist of the

testing procedures for the patient monitor 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 patient monitor

meets the performance specifications. If the patient monitor 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

z All tests should be performed by qualified service personnel only.
z Care should be taken to change the settings in [User Maintenance>>] and [Factory

Maintenance>>] menus to avoid loss of data.

z Service personnel should acquaint themselves with the test tools and make sure

that test tools and cables are applicable.

3.1.1 Test Equipment

See the following sections.

3.1.2 Test Report

Upon completion of the tests, the table of preventative maintenance test reports and the table

of maintenance test reports in this chapter should be kept properly.

3-1

3.1.3 Preventative Maintenance

Below are preventative maintenance tests which need to be performed on the monitor. See the

following sections for detailed maintenance procedures.

 Visual inspection
 NIBP test and calibration
 Microsteam and Sidestram CO

test and calibration

2

 AG test and calibration

3.1.4 Recommended Frequency

Check/Maintenance Item Frequency

Preventative Maintenance Tests

Visual inspection 1. When first installed or reinstalled.

NIBP test

Sidestream and

Microstream

tests

CO

2

AG tests

Performance Tests

Pressure check

Leakage test

Calibration

Leakage test

Performance test

Calibration

Performance test

Calibration

1. If the user suspects that the measurement is

incorrect.

2. Following any repairs or replacement of relevant

module.

3.At least once a year.

4. AG leakage test should be performed before AG

measurement.

Performance test

ECG test

Calibration

Resp performance test

SpO2 test

Pressure check

NIBP test

Leakage test

Calibration

Temp test

IBP test

Performance test

1. If the user suspects that the measurement is

incorrect.

2. Following any repairs or replacement of relevant

module.

3. At least once every two years. At least once a year

is recommended for NIBP, CO

NMT and AG.

2,

4. AG leakage test should be performed before AG

measurement.

3-2

C.O. test

Mainstream CO2 test

Pressure calibration

Sidestream and

Leakage test

Microstream

tests

CO

2

Performance test

Calibration

Leakage test

AG tests

Performance test

Calibration

ICG test

BIS test

RM test

Interconnecting

CCO/SvO2 test

function

Output calibration

NMT test

Performance test

Sensor check

EEG test

PiCCO test

ScvO2 test

Nurse call relay performance test

Analog output performance test

If the user suspects that the nurse call or analog

output does not work well.

Electrical Safety Tests

Electrical safety tests Refer to A Electrical Safety Inspection.

Other Tests

1. When first installed or reinstalled.

Power on test

2. Following any maintenance or the replacement of

any main unit parts.

Touchscreen calibration

1. When the touchscreen appears abnormal.

2. After the touchscreen is replaced.

Recorder check Following any repair or replacement of the recorder.

Network print test

1. When first installed.

2. Whenever the printer is serviced or replaced.

1. When first installed.

Device integration check

2. Following any repair or replacement of the

external device.

Battery check Functionality test

1. When first installed.

2. Whenever a battery is replaced.

3-3

3.2 Preventative Maintenance Procedures

3.2.1 Visual Inspection

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 case, display screen, buttons and knob for obvious signs of

damage.

 Inspect the SMR and parameter modules for obvious signs of damage.
 Inspect the power cord, wall-mount bracket and module accessories for obvious 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.

3-4

r

3.2.2 NIBP Tests

NIBP Accuracy Test

Tools required:

 T-shape connector
 Appropriate tubing
 Balloon pump
 Rigid Vessel with volume 500 ± 25 ml
 Reference manometer (calibrated with accuracy equal to or greater than 1 mmHg)

Follow this procedure to perform the test:

1. Connect the equipment as shown below.

Monito

Connector for NIBP cuff

Balloon

2. Before inflation, the reading of the manometer should be 0. If not, turn off the balloon

pump to let the whole airway open to the atmosphere. Turn on the balloon pump after

the reading is 0.

3. Select [Main Menu]→ [Maintenance >>]→ [NIBP Accuracy Test].

4. Check the manometer values and the monitor values. Both should be 0mmHg.

5. Raise the pressure in the rigid vessel to 50 mmHg with the balloon pump. Then, wait for

10 seconds until the measured values become stable.

Tubing

Manometer

Rigid vessel

6. Compare the manometer values with the monitor values. The difference should be 3

mmHg. If it is greater than 3 mmHg, contact your service personnel.

7. Raise the pressure in the rigid vessel to 200 mmHg with the balloon pump. Then, wait

for 10 seconds until the measured values become stable and repeat step 6.

3-5

NOTE

z You can use an NIBP simulator to replace the balloon pump and the reference

manometer to perform the test.

z You can use an appropriate cylinder and a cuff instead of the rigid vessel.

NIBP Leakage Test

NOTE

z You should perform NIBP accuracy test and make sure the test result is pass prior

to NIBP leakage test.

Tools required:

 NIBP cuff for adult patient
 Appropriate tubing
 Cylinder

Follow this procedure to perform the test:

1. Set [Patient Cat.] to [Adu].

2. Connect the NIBP cuff with the NIBP connector on the monitor.

3. Apply the cuff to the cylinder as shown below.

Monitor

Connector for

NIBP cuff

4. Select [Main Menu]→ [Maintenance>>]→ [NIBP Leakage Test]. The message

[Leakage Testing…] is displayed in the NIBP parameter area.

5. The cuff automatically deflates after 20s, which means NIBP leakage test is

completed.If no message is displayed in the NIBP parameter area, it indicates that the

system has no leakage. If the message [NIBP Pneumatic Leak] is displayed, it indicates

that the system may have a leakage. In this case, check if all connections are good and

the cuff and tubing have no leakage. Perform the test again after making sure all

connections are good and the cuff and tubing have no leakage.

Air tubing

Cylinder

Cuff

3-6

You can either perform a manual leakage test:

1. Perform procedures 1-4 in the NIBP Accuracy Test section.

2. Raise the pressure in the rigid vessel to 250 mmHg with the balloon pump. Then, wait

for 5 seconds to let the measured values becoming stable.

3. Record the current pressure value and meanwhile use a time counter to count time. Then,

record the pressure value after counting to 60s.

4. Compare the two values and make sure the difference should not be greater than 6

mmHg.

3.2.3 Sidestream and Microstream CO2 Module Tests

Leakage test

Follow this procedure to perform the test:

1. Plug the module into the module rack.

2. Wait until CO

warmup is finished and then use your hand or other objects to

2

completely block the gas inlet of the module or watertrap. The sidestream and

microstream CO

 Sidestream: The alarm message [CO

modules will behave as follows:

2

FilterLine Err] is displayed on the screen

2

after 3 seconds. Block the gas inlet for another 60 s. Select [Main Menu]→
[Maintenance >>]→[User Maintenance >>] → enter the required password →

[Maintain CO

>>]→ [Calibrate CO2 >>], and check that the flow rate is less than.

2

10ml/min. The module does not leak if current flow rate is less than 10ml/min and

the alarm message does not disappear.

Microstream: The alarm message [CO2 Purging] is displayed on the screen after



certain time. Block the gas inlet for another 30s. If alarm message [CO

Err] is shown, it indicates that the module does not leak.

FilterLine

2

3-7

Accuracy Test

Tools required:

 A steel gas cylinder with 6±0.05% CO

and balance gas N2

2

 T-shape connector
 Tubing
 Flowmeter

Follow this procedure to perform the test:

1. Plug the module into the module rack.

2. Wait until the CO

module warmup is finished, and check the airway for leakage and

2

perform a leakage test as well to make sure the airway has no leakage.

3. Enter [User Maintenance]→ [Maintain CO

>>]→ [Calibrate CO2>>].

2

4. Connect the test system as follows:

Flowmeter

Tubing

Relief valve

Monitor

T shape connector

Gas cylinder

5. Open the relief valve, and adjust it until the flowmeter has a stable reading between 10

ml/min and 50ml/min.

6. Check the realtime CO

value is within 6±0.05％ in the [Calibrate CO2] menu.

2

3-8

Calibration

Tools required:

 A steel gas cylinder with 6±0.05% CO

and balance gas N2

2

 T-shape connector
 Tubing
 Flowmeter

Follow this procedure to perform a calibration:

1. Make sure that the sidestream or microstream CO

module has been warmed up or

2

started up.

2. Check the airway for leakage and perform a leakage test as well to make sure the airway

has no leakage.

3. Select [Main Menu]→ [Maintenance >>]→ [User Maintenance >>]→ enter the

required password→ [Maintain CO

4. In the [Calibrate CO

] menu, select [Zero].

2

>>]→ [Calibrate CO2 >>].

2

5. After the zero calibration is finished successfully, connect the equipment as follows:

Flowmeter

Tubing

Relief valve

Monitor

T shape connector

Gas cylinder

6. Open the relief valve, and adjust it until the flowmeter has a stable reading between 10

ml/min and 50ml/min.

7. In the [Calibrate CO

8. In the [Calibrate CO

measured CO

concentration becomes stable, select [Calibrate CO2] to calibrate the

2

] menu, enter 6% (the CO2 concentration) in the [CO2] field.

2

] menu, the measured CO2 concentration is displayed. After the

2

CO2 module.

3-9

If the calibration is finished successfully, the message [Calibration Completed!] is

displayed in the [Calibrate CO2] menu. If the calibration failed, the message [Calibration

Failed!] is displayed. In this case, perform another calibration.

3.2.4 AG Tests

AG Leakage Test

The AG leakage test is required every time before the AG measurement. Follow this

procedure to perform the test:

1. Plug the AG module into the module rack.

2. Wait for more than10mins until the AG module warmup is finished and then use your

hand or other objects to completely block the gas inlet of the AG module. An alarm

message [AG Airway Occluded] will appear on the screen.

Block the gas inlet for another 30 s. Select [Main Menu]→[Maintenance >>]→[User

3.

Maintenance >>]→enter the required password→Module Maintenance >>]→

[Calibrate AG >>].

Check that the current flow rate is less than 10ml/min, and the alarm message [AG Airway

Occluded] does not disappear. This indicates that the module does not leak.

If the alarm message disappears, or the flow rate is equal to or greater, it indicates that the

module leaks. Perform the leakage test again. If the problem remains, contact your service

personnel for help.

AG Accuracy Test

Tools required:

 Gas cylinder with 100% O

or standard gas mixture (such as 5±0.03% CO2, 1.5±0.15% ISO, 45±0.23% O2 bal N2O).

 Gas concentration should meet the following requirements respectively: AA≥1.5%,

CO2≥1.5%, N2O≥40%, O2≥40%, of which AA represents an anaesthetic agent. The gas

concentration accuracy should have a tolerance as follows: AA±0.15%, CO2±0.1%,

N2O±1%, O2±1%.

and/or a certain standard gas (such as 6±0.05% CO

2

, Bal N2),

2

 T-shape connector

 Tubing

3-10

NOTE

 When testing a particular gas in a mixture, only the concentration of the gas to be

tested needs to meet the requirements.

 Handle the gas cylinder by following the instructions on the gas cylinder.

Follow this procedure to perform the test:

1. Plug the AG module into the module rack.

2. Wait at least 10 min and then perform a leakage test to make sure the airway has no

leakage.

3. Check if the fan inside the AG module works correctly.

4. Connect the test system as follows:

Open to the air

Relief valve

T-shape connector

Gas cylinder

5. Open the relief valve and vent a standard gas and make sure that there is an excess gas

flow through the T-shape connector to air. And wait for at least 30 seconds until the gas

reading stable.

6. Check that the concentration of each composition meets the specification stated in the

Operator's Manual.

Tubing

Monitor

WARNING

 When performing AG accuracy test, be sure to dispose of exhaust gas properly.

3-11

AG Calibration

Tools required:

 Gas cylinder with a certain standard gas or standard gas mixture. Gas concentration

should meet the following requirements respectively: AA≥1.5%, CO2≥1.5%, N2O≥40%,

O2≥40%, of which AA represents an anaesthetic agent. The gas concentration accuracy

should have a tolerance as follows: AA±0.15%, CO2±0.1%, N2O±1%, O2±1%.

 T-shape connector

 Tubing

NOTE

 When calibrating a particular gas in a mixture, only the concentration of the gas to

be calibrated needs to meet the requirements.

 Handle the gas cylinder by following the instructions on the gas cylinder(s).

Follow this procedure to perform the AG calibration:

1. Select [Main Menu]→[Maintenance >>]→[User Maintenance >>]→enter the

required password→[Module Maintenance >>]→[Calibrate AG >>]..

2. Check the airway and make sure that there are no occlusions or leaks.

 Vent the sampling tubing to the air and check if the [Current FlowRate] and

[SetFlowRate] are approximately the same. If the deviation is great, it indicates

that there is an occlusion in the tubing. Check the tubing for an occlusion.

 Perform a leakage test to make sure that the airway has no leakage.

3. Connect the test system as follows:

Open to the air

Relief valve

T-shape connector

Tubing

Monitor

Gas cylinder

4. Open the relief valve and vent a certain standard gas or gas mixture and make sure that

there is an excess gas flow through the T-shape connector to air. And wait for at least 30

seconds until the gas reading stable.

3-12

5. In the [Calibrate AG] menu, the concentration of each measured gas and flow rate are

displayed.

 If the difference between the measured gas concentration and the actual one is

within the tolerances in the user manual, a calibration is not needed.

 If the difference for one gas composition or more gas compositions is outside of the

stated tolerances, a calibration for one gas composition or more gas compositions

should be performed. Select [Calibrate >>] to enter the calibrate menu.

6. Enter the vented gas concentration(s) for one gas composition or more gas compositions

which needs calibration. If only one gas composition in gas mixture is to be calibrated

i.e. CO

only, set the concentration of the other gases to 0.

2

7. Select [Start] to start a calibration.

8. If the calibration is finished successfully, the message [Calibration Completed!] is

displayed. If the calibration failed, the message [Calibration Failed!] is displayed.

Perform another calibration.

After the calibration finished, an accuracy test should be performed according to the

Accuracy Test chapter. If one gas composition of the gas mixture is outside of the stated

tolerances, please perform the calibration for the gas which reading is out of stated tolerances

by using the calibration gas cylinder or another calibration gas cylinder following the

instruction of Calibration chapter again.

WARNING

 When performing AG calibration, be sure to dispose of exhaust gas properly.

CAUTION

 Calibrate the AG module, if it has been transported for a long distance or not used

for a prolonged period of time.

 Calibrate the AG module, if the module was subject to physical impact damage i.e.

dropped etc. or when the measured value(s) has a great deviation.

NOTE

 For measurement of O

cylinder with 100% O2 to do the O2 calibration again.

concentration more than 80%, it recommends to use gas

2

3-13

3.2.5 Preventative maintenance test report

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

Test items Test records Test results

(Pass/Fail)

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

3-14

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

Filterline Err is given. It indicates that there is no leakage.

The displayed CO2 value is within 6±0.05％.

AG test

When AG flowrate is slower than 10ml/min, an alarm of AG

Airway Occluded is given. It indicates that there is no leakage.

The fan inside the AG module works properly.

The measurement accuracy of CO2, N2O, O2 and AA (AA

represents an anaesthetic agent) meets the product specifications

in the Operator’s Manual.

3-15

3.3 Power On Test

This test is to verify that the patient monitor can power up correctly. The test is passed if the

patient monitor starts up by following this procedure:

1. Insert two batteries in the battery chamber and connect the patient monitor to the AC

mains, the AC mains LED and battery LED light.

2. Press the power on/off switch to switch on the patient monitor. The operating status

LED lights up, and the technical and physiological alarm lamps light blue and red

respectively.

3. After the start-up screens are displayed, the system sounds a beep indicating the self test

on alarm sounds is passed. At the same time, the alarm lamp turns from yellow to red,

and then turns off together with the technical alarm lamp. This indicates that the self test

on alarm lamps is passed.

4. The patient monitor enters the main screen and start-up is finished.

3.4 Module Performance Tests

3.4.1 ECG Tests

ECG Performance Test

Tool required:

 Fluke Medsim 300B patient simulator recommended

Follow this procedure to perform the test:

1. Connect the patient simulator with the ECG module using an ECG cable.

2. Set the patient simulator as follows: ECG sinus rhythm, HR=80 bpm with the amplitude

as 1mV.

3. Check the ECG waves are displayed correctly without noise and the displayed HR value

is within 80 ± 1 bpm.

4. Disconnect each of the leads in turn and observe the corresponding lead off message

displayed on the screen.

5. Set that the simulator outputs paced signals and set [Paced] to [Yes] on the monitor.

Check the pace pulse marks on the monitor screen.

3-16

ECG Calibration

Tool required:

 Vernier caliper

Follow this procedure to perform a calibration:

1. Select the ECG parameter window or waveform area→ [Filter]→ [Diagnostic].

2. Select [Main Menu]→ [Maintenance>>].

3. Select [Calibrate ECG]. A square wave appears on the screen and the message [ECG

Calibrating] is displayed.

4. Compare the amplitude of the square wave with the wave scale. The difference should

be within 5%.

5. After completing the calibration, select [Stop Calibrating ECG].

If necessary, you can print out the square wave and wave scale through the recorder and then

measure the difference.

3.4.2 Resp Performance Test

Tool required:

 Fluke Medsim 300B patient simulator recommended

Follow this procedure to perform the test:

1. Connect the patient simulator to the module using a non ESU-proof cable and set lead II

as the respiration lead.

2. Configure the simulator as follows: lead II as the respiration lead, base impedance line

as 1500 Ω; delta impedance as 0.5 Ω, respiration rate as 40 rpm.

3. Check the Resp wave is displayed without any distortion and the displayed Resp value is

within 40 ± 2 rpm.

3-17

3.4.3 SpO2 Test

Tool Required:

 None.

Follow this procedure to perform the test:

1. Connect SpO2 sensor to the SpO2 connector of the monitor. Set [Patient Cat.] to [Adu]

and [PR Source] to SpO2 on the monitor.

2. Measure SpO

3. Check the Pleth wave and PR reading on the screen and make sure that the displayed

is within 95%-100%.

SpO

2

4. Remove the SpO

Off is triggered.

on your finger. (Assume that you stay healthy)

2

sensor from your finger and make sure that an alarm of SpO2 Sensor

2

NOTE

z A functional tester cannot be used to assess the accuracy of a pulse oximeter

monitor. However, it can be used to demonstrate that a particular pulse oximeter

monitor reproduces a calibration curve that has been independently demonstrated

to fulfill a particular accuracy specification.

3.4.4 NIBP Tests

See section 3.2.2 NIBP Tests.

3.4.5 Temp Test

Tool required:

 Resistance box (with accuracy above 0.1Ω)

Follow this procedure to perform the test:

1. Connect the two pins of any Temp connector of a module to the two ends of the

resistance box using 2 wires.

2. Set the resistance box to 1354.9Ω (corresponding temperature is 37ºC).

3. Verify each Temp channel of the monitor and make sure that the displayed value is

within 37 ± 0.1ºC.

You can also use a patient simulator to perform the Temp test.

3-18

3.4.6 IBP Tests

IBP Performance Test

Tool required:

 Medsim300B patient simulator, MPS450, or other equivalent device
 Dedicated IBP adapter cable (300B, P/N 00-002199-00) (use P/N 00-002198-00, if the

simulator is MPS450)

Follow this procedure to perform the test:

1. Connect the patient simulator with the pressure module.

2. Make the patient simulator outputs 0 to each IBP channel.

3. Press the Zero Key on the module to make a zero calibration.

4. Configure the patient simulator as P (static) = 200 mmHg.

5. The displayed value should be within 200 ± 2 mmHg.

6. If the value is outside of these tolerances, calibrate the pressure module. If the IBP

module was calibrated with a dedicated reusable IBP sensor, check the calibration

together with this IBP sensor.

7. Make that the patient simulator outputs 120/80 mmHg ART signals and 120/0 mmHg

LV signals respectively to each IBP channel and check that the IBP wave is displayed

correctly.

8 Repeat the steps above for all the IBP channels.

IBP Pressure Calibration

Method 1:

Tools required:

 Medsim300B Patient simulator, MPS450, or other equivalent device
 Dedicated IBP adapter cable (300B, P/N 00-002199-00) (use P/N 00-002198-00, if the

simulator is MPS450)

Follow this procedure to perform the test:

1. Connect the patient simulator to the pressure connector on the module.

2. Set the patient simulator to 0 pressure for the desired IBP channel.

3. Press the Zero Key on the module to make a zero calibration.

4. Configure the patient simulator as P (static) = 200 mmHg.

5. Select [Main Menu]→ [Maintenance >>]→[User Maintenance >>] →[Cal. IBP

Press. >>]. In the [Cal. IBP Press.] menu, set the calibration value to 200 mmHg.

3-19

k

6. Select the [Calibrate] button next to the desired IBP channel to start a calibration.

7. If the calibration is completed successfully, the message [Calibration Completed!] will

be displayed. Otherwise, a corresponding message will be displayed.

Method 2:

Tools required:

 Standard sphygmomanometer
 Balloon pump
 Tubing
 T-shape connector

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.

3. Press the Main menu button on the equipment’s front panel. Select [Maintenance>>]→

[User Maintenance >>]→ enter the required password→[Cal. IBP Press. >>]. 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 stopcoc

T-shape connector

Sphygmomanometer

Pressure adapter cable

IBP Module

5. Adjust the calibration value in the [Cal. IBP Press.] 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.

3-20

3.4.7 C.O. Test

Tools required:

 Medsim300B Patient simulator
 C.O. adapter box

Follow this procedure to perform the test:

1. Connect the patient simulator to the C.O. module using a C.O. main cable.

2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the

temperature value is 37 ± 0.1ºC.

3. Set [Auto IT] to [Off] and adjust [IT] to 24ºC. Select [C.O. Measure] to enter the C.O.

measurement window and set [Comp. Const.] to 0.595.

4. Set the injectate temperature to 24ºC and the C.O. to 5L/min on the C.O. simulator.

Select [Start] in the C.O. measurement window to start C.O. measurements and after

3-10 seconds press the run key on the simulator.

5. Check the C.O. value is 5±0.25L/min.

3.4.8 Mainstream CO2 Tests
NOTE

z Make sure that the barometric pressure set in [Maintain CO

Maintenance>>] accords with the local barometric pressure before performing

mainstream CO

Tools required:

 A steel gas cylinder with 6±0.05% CO
 A steel gas cylinder with compressed air or N
 Two 3-way valves (power supply controlled)
 Flowmeter
 Power supply

tests.

2

2

(with standard concentration)

2

>>] of [User

2

 Tube

Follow this procedure to perform the test:

1. Wait until CO

warmup is finished and then select [Start Zero Cal.] from [CO2 Setup]

2

menu to start a zero calibration. If the zero calibration fails, the prompt message [CO

Zero Failed] is displayed. Otherwise, the baseline of waveform recovers to zero.

2 Set [Apnea Time] to 10 s in the [Adjust CO

Limits] menu.

2

3-21

2

3 Blow to the CO2 sensor to generate a CO2 waveform and then place the sensor in the air.

Check if the alarm message [CO

Apnea] is displayed on the screen.

2

4 Connect the test system as follows

Indication of numbers in the figure above

1 A steel gas cylinder with 6±0.05% CO

2

2 Flowmeter

3 3-way valve (power supply controlled)

4 Open to air

5 Power supply (controlling two 3-way valves)

6 Compressed air or N2 with standard concentration

7 Mainstream CO2 sensor

8 Patient monitor

9 Tube (preventing back flow)

5 Adjust the power supply and turn on/off 3-way valves to ensure that that only one

cylinder is connected to Mainstream CO

sensor via 3-way valves at one time and the

2

flowmeter reading is stable and within 2-5L/min.

6 Switch between the two cylinders to connect Mainstream CO

-10s and check if the displayed CO

value is within 6±0.05％.

2

3-22

sensor at intervals of 6

2

3.4.9 Sidestream and Microstream CO2 Module Tests

See section 3.2.3 Sidestream and Microstream CO2 Module Tests.

3.4.10 AG Tests

See section 3.2.4 AG Tests.

3.4.11 ICG Test

Tool required:

 ICG simulator (BZ-4575)

1. Connect the ICG simulator and the patient monitor using standard ICG cable and sensor.

2. Select [ICG setup]→ [Patient Demographics >>] and then input parameter values as

follows:

Height 180 cm CVP 6 mmHg

Weight 75 kg PAmean 8 mmHg

PAWP 10 mmHg

3. Switch on the simulator and set as follows: HR=60±1 bpm, VI=61±4/1000s,

TFC=32±2/kOhms. Then, start ICG monitoring.

4. After the measurement becomes stable and check that the measured results are as

follows: HR=60±2 bpm, VI=61±4/1000s, TFC=32±2/kOhms.

5. Set on the simulator as follows: HR=70±1 bpm, VI=48±4 /1000s, TFC=32±2 / kOhms,

and then start ICG monitoring. After the measurement becomes stable and check that the

measured results are as follows: HR=70±2 bpm, VI=48±4 /1000s, TFC=32±2 / kOhms.

3-23

3.4.12 BIS Test

You can choose either of the following methods to perform the test:

Method 1:

Tools required:

 None.

1. Connect the BIS sensor to a healthy, wide-awake adult as directed in the Operator’s

Manual.

2. Check the EEG wave and BIS numerics displayed on the screen and make sure the BIS

value is within 80-100.

Method 2:

Tools required:

 BIS simulator (with flexible cable)

1. Connect the BIS sensor with the BIS simulator and select [BIS Setup]→ [BIS Sensor

Check] to perform a cyclic impedance check.

2. After the cyclic impedance check is finished, check that the result for each electrode is

pass.

3. Check the EEG wave and BIS numeric displayed on the screen.

3-24

3.4.13 RM Test

Tool required:

 Gas source
 Ventilator (calibrated)
 Artificial lung
 Pediatric/neonate flow sensor

Ventilator

Monitor

Artificial

lung

Flow sensor

Follow this procedure to perform the test:

1. Connect the equipment as shown above. Make sure that the blue sensing tube on the

flow sensor is connected with the artificial lung.

2. Set [Patient Cat.] to [Adu]. In the [RM Setup] menu, select [Sensor Type] according

to the used sensor and set [Ventilation Mode] to [Mechanical].

3. Enter the [RM Setup] menu and select [Calibrate >>]. Input the constant marked on

the sensor and calibrate the flow sensor.

4. Configure the ventilator as follows: TV=500 ml, RR =20 rpm, I:E=1:2.

5. Select [Respiratory Loop] in the [RM Setup] menu. Verify that the displayed TV is

within 500±50ml and RR is within 20±1rpm.

3-25

3.4.14 CCO/SvO2 Tests

Interconnecting Function

Tools required:

 None.

1. Connect and set the patient monitor and Vigilance monitor per the procedures in the

Operator’s Manual.

2. Set the Vigilance monitor to Demo mode.

3. Check that the CCO/SvO

numerics displayed on the patient monitor and Vigilance

2

monitor are consistent.

Output Performance

Tools required:

 Oscillograph

1. Connect the signal output end of the connecting cables of the CCO/SvO

oscillograph.

2. Make the monitor to perform an ECG calibration. Check that the ECG waves displayed

on the oscillograph are consistent with the ECG calibration waves displayed on the

monitor screen.

3. Select [CCO Setup]→ [Signal Output Setup >>] and then select [Simulated High

Value] from the pop-up menu. Check that the amplitude of electrical level at the signal

output port of MAP, CVP and SpO

are 5±0.25V, 5±0.25V and 10±0.5V respectively.

2

module to the

2

3-26

3.4.15 PiCCO Tests

Performance Test

Tool required:

 Medsim300B patient simulator
 PiCCO IBP test cable (6800-J87)

Follow this procedure to perform the test:

1. Connect the patient simulator, the PiCCO IBP test cable and the PiCCO module.

2. Let the patient simulator outputs 0 mmHg respectively to the pArt channel and the

pCVP channel.

3. In the [pArt Setup] menu, select [pArt Zero >>]→[Zero].

4. In the [pCVP Setup] menu, select [pCVP Zero >>]→[Zero].

5. Let the patient simulator output static pressure 200 mmHg to pArt channel and 20

mmHg to pCVP channel.

6. The pArt value displayed on the monitor should be within 200 ± 4 mmHg, and pCVP

value within 20 ± 1 mmHg.

7. If the pArt error is beyond ±4 mmHg or pCVP error beyond ±1 mmHg, calibrate the

PiCCO module. If the module was calibrated with a dedicated reusable IBP sensor,

check the calibration together with this IBP sensor.

8. Let the patient simulator output ART signal to the pArt channel and pCVP signal to the

pCVP channel, verify that the pArt and pCVP waves are displayed correctly.

Pressure Calibration
Method 1

Tools required:

 Medsim300B patient simulator
 PiCCO IBP test cable (6800-J87)

Follow this procedure to perform the test:

1. Connect the patient simulator, the PiCCO IBP test cable and the PiCCO module.

2. Let the patient simulator outputs 0 mmHg respectively to the pArt channel and the

pCVP channel.

3. In the [pArt Setup] menu, select [pArt Zero >>]→[Zero].

4. In the [pCVP Setup] menu, select [pCVP Zero >>]→[Zero].

5. Set static pressure to 200 mmHg on the patient simulator.

3-27

6. Select [Main Menu]→[Maintenance >>]→[User Maintenance >>]→ [Cal. IBP

Press. >>]. In the [Cal. IBP Press.] menu, set the calibration pressure to 200 mmHg.

7. Select the [Calibrate] button next to the desired IBP channel to start a calibration.

If the calibration is completed successfully, the message [Calibration Completed!] will be

displayed. Otherwise, a corresponding message will be displayed.

Method 2

Tools required:

 Standard sphygmomanometer
 Balloon pump
 Tubing
 T-shape connector

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. Vent the transducer to the atmospheric pressure by turning on the 3-way stopcock to the

air. Zero the transducer, and then open the stopcock to the sphygmomanometer.

3. Select [Main Menu]→[Maintenance >>]→ [User Maintenance >>]→enter the

required password→ [Cal. IBP Press. >>]. In the [Cal. IBP Press.] menu, set the

calibration pressure to 200 mmHg.

4. Inflate using the balloon pump until the reading of sphygmomanometer approximates

the preset calibration value.

Pressure transducer

3-way stopcock

T-shape connector

Sphygmomanometer

Pressure adapter cable

IBP Module

5. Adjust the calibration value in the [Maintain IBP] menu until it is equal to the reading

of sphygmomanometer

6. In the [Cal. IBP Press.] menu, select the [Calibrate] button next to the desired IBP

channel to start a calibration

3-28

The message [Calibration Completed!] is displayed after a successful calibration. If the

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

C.O. Test

Tools required:

 Medsim300B Patient simulator, or equivalent equipment
 C.O. adapter box (for 300B)
 PiCCO test cable (PN: 040-001301-00)

Follow this procedure to perform the test:

1. Connect the patient simulator and the C.O. module using a C.O. trunk cable and a C.O.

adapter box.

2. Set the blood temperature (BT) to 37ºC on the patient simulator and check the

temperature value displayed on the monitor is 37 ± 0.1ºC.

3. In the [CCO Setup] menu, select [PiCCO Guide>>], and check if the value for

[Cat.Type] is [PV2015L20].

4. Turn the injectate temperature (TI) knob on the C.O. adapter box to set the TI to 20 ±

1ºC for the patient simulator and C.O. to 5L/min.

5. In the PiCCO screen, select [Start] to start C.O. measurement. As soon as the prompt

[Inject XXml] is displayed, adjust TI to 4 ± 1ºC, and then quickly back to 20 ± 1ºC.

Simutaneously press the button on the simulator that corresponds to 5L/min. The whole

procedure shall be finished in 10 s.

6. Verify that the C.O. value displayed on the monitor is correct.

3-29

3.4.16 ScvO2 Tests

You can perform ScvO2 test by either of the following two methods:

Method 1:

Tools required:

 PC (installed OM_Simulation software, G-6800-S15)
 ScvO

test cable (6800-J68)

2

1. Connect the ScvO

test cable to the ScvO2 module and the serial port on the PC

2

respectively;

2. Open ScvO

test software to select the corresponding serial port from [COM port]

2

menu (default serial port: COM1);

3. Select [Start] from the [Replay] menu. Then the ScvO

measurement area is displayed

2

on the patient monitor;

4. Enter [ScvO

Setup] menu and set [Hb/Hct] to [Hct];

2

5. Set [LED660], [LED800], [LED880] to ‘1250，40000’ (inching with the direction key

on the keyboard if needed). Select [Start] from the [Replay] menu;

6. Enter [ScvO

Calibration] menu and select [Sample drawn] when SQI occupies four

2

grids (80%). In the popup menu, set [ScvO2] and [Hct] to 67％ and 40％ respectively,

then select [Calibrate]. Close [ScvO

Calibration] menu to check that the ScvO2 value

2

is displayed as 67％ in the monitoring screen.

7. Set the value of [LED660] to ‘1250, 33600’ and keep other LCD values unchanged.

Check that the ScvO2 measurement is within (50±3)%.

8. Set the value of [LED660] to ‘1250, 46400’ and keep other LCD values unchanged.

Check that the ScvO

measurement is within (80±3)%.

2

Method 2:

Tools required:

 None.

1. Connect the ScvO

sensor to the patient monitor. Check that the front end of the ScvO2

2

sensor illuminates normally.

2. Nip the front end of the ScvO

3. Check that the patient monitor displays the ScvO

sensor with two fingers to perform a ScvO2 calibration.

2

measurement normally.

2

3-30

3.4.17 NMT Tests

NMT Performance Test

Tool required:

 Resistance box

Oscillograph (Agilent DSO6052A)



1. Set up the resistance box:

a. Set the resistance value to 1kOhm.

b. Connect the stimulation electrodes to the two wiring terminals.

2. Connect the oscillograph sensors to the NMT stimulation electrodes, making sure that

each sensor and electrode connected have the same polarity.

3. Set up the monitor:

a. Insert the NMT module into the module rack of the monitor.

b. Set the [Stimulation Current] to [Supra(60mA)].
c. Set the [Pulse Width] to 300μs.

d. Perform an ST measurement.

4. Proceed as follows to capture the pulse signals and measure the [PK-P K] and [+Width].

The following procedures take the oscillograph of Agilent DSO6052A as an example.

a. Power on the oscillograph by pressing the [POWER] button. Select the button [1] and

verify the button light is on.

b. Press the [Mode/Coupling] button, and select [Normal], [Noise REJ] and [HF

Reject] at the lower part of the screen.

c. Press the [Acquire] button, and select [High Resolution] from the dropdown list of

[Acq Mode].

d. Press the [Quick Meas] button. Select [PK-PK] from the dropdown list of [Select]

and select [Measure] to confirm; select [+Width] from the dropdown list of [Select]
and then select [Measure] to confirm.

e. In the [Horizontal] area, adjust [Delay] to 0.0s by using the [◀▶] knob, and adjust the

numeric value to 100ms by using the big knob.

f. In the [Analog] area, adjust the numeric value to 20.0V by using the big knob and

adjust the [Ch(1)] to 40.0V by using the [

g. Press the [Edge] button. Select [1] from the dropdown list of [Source]; select [Rising]

from the dropdown list of [Slope].

h. In the [Trigger] area, adjust the numeric value to 40.0V by using the [Level] knob.

Press [Single] to perform a measurement.

] knob.

3-31

The test passes when the measurements are within the following ranges:

Test items Measurements

【PK-PK】 54V - 66V

【+Width】 270μs - 330μs

Checking NMT Sensor

Tools required:

 None

1. Connect the patient monitor, NMT module, and NMT accessories.

2. Select [Main Menu]→ [Maintenance >>]→ [User Maintenance >>]→ enter the

required password→ [NMT Sensor Check >>] from the patient monitor.

3. Follow the on-screen instructions to check the NMT sensor in four ways.

If sensor check completes successfully, the message “Test passed. The function of NMT

sensor is OK” is presented. If any of the four steps fails, check if the sensor is placed

correctly as instructed, and perform the sensor check again. Replace the sensor if you cannot

pass the sensor check..

NOTE

z Stop NMT measurement or calibration before starting NMT sensor check.
z Take care to handle the the NMT sensor. Avoid forcefully striking the sensor.

3-32

3.4.18 EEG tests

Method 1

Tools required:

 EEG simulator (Nannini 169/1)

1. Insert the EEG module into the module slot of the monitor.

2. Connect the EEG module to the EEG simulator through the EEG patient cable.

3. Select [EEG Setup]→ [Sensor Check] to perform a sensor check.

4. Check that the result for each electrode is pass.

5. Check that the EEG wave and numeric are displayed on the screen.

Method 2

Tools required:

 None

1. Insert the EEG module into the module slot of the monitor.

2. Connect the EEG cable and EEG electrodes to the EEG module, and short all the

electrodes.

3. Select [EEG Setup]→ [Sensor Check] to perform a sensor check.

4. Check that the result for each electrode is pass.

5. Check that the EEG wave and numeric are displayed on the screen.

3-33

3.5 Nurse Call Relay Performance Test

Tools required:

 Multimeter

1. Connect the nurse call cable to the Nurse Call Connector of the patient monitor.

2. Enter Demo mode. Then, select [Main Menu]→ [Maintenance >>]→ [User

Maintenance >>]→ enter the required password→ [Others >>]→ [Auxiliary

Output]→ [Nurse Call].

3. In the [Others >>] menu, select [Nurse Call Setup >>] and then select all options of

[Alm Lev] and [Alarm Cat.] and set [Contact Type] to [Normally Open]

4. In [Nurse Call Setup >>] setup menu, set [Signal Type] to [Pulse]. Make the monitor

to generate an alarm and check that the output are pulses of 1s width and the relay

contacts are close (can be measured with a multimeter) when there is an alarm.

5. In [Nurse Call Setup >>] setup menu, set [Signal Type] to [Continuous].Make the

monitor to generate an alarm and check that the output is continuous high level and the

relay contacts are close (can be measured with a multimeter) when there is an alarm.

3.6 Analog Output Performance Test

Tool required:

 Patient simulator
 Oscillograph

1. Connect the patient simulator to the monitor using an ECG or IBP cable and connect the

oscillograph to the Auxiliary Output Connector of the patient monitor.

2. Select [Main Menu] → [Analog Output Setup]. Switch Analog Output [On].

3. Verify that the waves displayed on the oscillograph are identical with those displayed on

the monitor.

3.7 Electrical Safety Test

See A Electrical Safety Inspection for electrical safety tests.

3-34

3.8 Touchscreen Calibration

Tools required:

 None.

1. Select the [Cal. Screen] QuickKey or select [Main Menu]→ [Maintenance >>]→

[User Maintenance >>]→ enter the required password→ [Cal. Touchscreen].

2. The

3. Select, in turn, the central point of the

4. After the calibration is completed, the message [Screen Calibration Completed!] is

displayed. Select [Ok] to confirm the completion of the calibration.

symbol will appear at different positions of the screen.

symbol.

3.9 Recorder Check

Tools required:

 None.

1. Print ECG waveforms. The recorder should print correctly and the printout should be

clear.

2. Set the recorder to some problems such as out of paper, etc. the patient 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.

3.10 Network Print Test

Note

z HP LaserJet 1505n, P2035n, P4015n, or 1606dn laser printer is recommended for

BeneView series of patient monitors.

Tools required:

 Hub and network cable

3-35

3.10.1 Equipment Connection and Setup

1. Connect the patient monitor and network printer to a HUB using common network

cables as follows:

BeneView

monitor

Cable Cable

HUB

2 Set IP address as follows: Select [Main Menu]→ [Maintenance >>]→ [User

Maintenance >>]→ enter the required password→ [IP Address Setup >>] and set the

IP address of the patient monitor in the same network segment with that of the network

printer. (See the instructions for use accompanying the printer)

3 Search for printer by selecting [Main Menu]→ [Print Setup >>]→ [Printer Setup

>>]→ [Search Printer]. After a while, the printer’s model and IP address will appear in

the box beside [Printer].

Network

printer

3.10.2 Print Function Test

1 Enter the Demo mode of the patient monitor.

2 Select [Main Menu]→ [Print Setup >>]→ [Realtime Reports >>]→ [Normal Report]

and then select [Print]. The network printer shall print out the report correctly.

3-36

3.11 BeneLink Module Check

3.11.1 Device Connection and Setup

Tools required:

 External device (anesthesia machine, ventilator)
 ID adapter that maches the external device
 RJ45 connecting cable
 Serial port adapting cable that maching the external device

Please refer to the following procedure to connect an external device:

BeneLink Module

Label

1. Insert the BeneLink module into the module slot on the BeneView patient monitor.

2. Connect the ID adapter that matches the external device to the BeneLink module with a

RJ45 connecting cable.

RJ45 Connecting

Cable

ID Adapter

Serial Port Adapting

Cable (Optional)

External Device

3. Plug the ID adapter into the RS232 port on the external device. Some external devices

may have ports incompatible with the ID adapter. In this case, a serial port adapting

cable is required. Please be sure that you have selected the proper cable before

connection.

4. Stick a label indicating device name to the RJ45 connecting cable at the end nearby the

BeneLink module. When the BeneLink module is connected to several external devices,

you can tell the devices apart easily with these labels.

5. Switch the external device on.

3-37

NOTE

z Devices of the same category can not be connected to the BeneLink module

simultaneously.

z Use the serial port adapting cable only with its matching extermal device. Please see

the following table to select the correct adapting cable.

z Use the ID adapter only with the matching external device. Please see the following

table for correct ID setup in [Factory Maintenance] menu.

External Device ID for ID adapter

Mindray Wato 20/30/55/65 4D52B2AE

Newport E360 4E50B1B0 Type B

SNDF：5042AFBE
（recommended）

Puritan Bennett 840

Maquet Flow-i 4D46B2BA Type B

Maquet Servo-i/Servo-s 4D53B2AD Type B

Draeger Evita 2 / Evita 2 dura

/ Evita 4/ Evita XL

Hamilton G5 (protocol

Polling)

SNDA：5031AFCF（support

less parameters than protocol
SNDF）

4434BBCC Type B

3550CAB0 Type B

Type of Serial Port Adapting

Cable

No need to use the adapting

cable: the ID adapter can be

plugged into the serial port of

the external device directly.

No need to use the adapting

cable: the ID adapter can be

plugged into the serial port of

the external device directly.

Hamilton C2 (protocol

Polling)

Hamilton Galileo (protocol

Polling)

Hamilton G5 (protocol Block) 3542CABE Type B

Ohmeda Avance/Aisys 4F41B0BF Type D

Ohmeda Aestiva 7100/7900 4F37B0C9 Type D

3270CD90 Type B

4750B8B0 Type B

3-38

External Device ID for ID adapter

Drager Fabius GS/Plus/Trio 4446BBBA

Drager Primus 4450BBB0 Type C

TCM CombiM/TCM TOSCA 5443ABBD Type C

TOF-Watch SX 5457ABA9 Type C

Expand Model / Type A

Type of Serial Port Adapting

Cable

GS: no need to use the

adapting cable: the ID adapter

can be plugged into the serial

port of the external device

directly.

Plus: type C

Trio: type C

3.11.2 Device Integration Function Test

3.11.2.1 Preparation

Prepare the tools needed for function test according to the type of the external device you

install. Please see the Instructions for Use of the corresponding external device for guidance.

For the function test of ventilator and anesthesia machine, at least the following tools are

needed:

 BeneView patient monitor with BeneLink module properly installed
 External device (anesthesia machine or ventilator) under test
 Gas source(tube or gas cylindar), including air or O

anesthesia gases are optional

 Tube that connects the patient(or test lung)
 Test lung and a matching Y-pipe, or other accessories

at least, and N2O or other

2

3.11.2.2 Procedure and Items to Be Checked

Follow the steps below:

1. Connect the BeneLink module to the ventilatior or the anesthesia machine. Plaese see

Device Connection and Setup for more details.

2. Connect the gas supply and test lungs to the ventilator or anesthesia machine, turn on the

device, and configure as follows:

 Setup up the serial port of the external device by refering to Serial Port

Configuraion List.

3-39

 Setup up the pressure control mode and check if the ventilator or anesthesia

machine works normally.

3. Check the ID adapter is correctly configured, and the green indicator of corresponding

port on the BeneLink module illuminates constantly.

4. Access [Devices Integrated] screen on the patient monitor. Check that the device type

(ventilator or anesthesia machine) and ventilation mode are correctly displayed.

5. Select parameters PEEP, Pmean, VTe, MV, I:E, and f(RR) respectively on the patient

monitor and check if the parameter values displayed on the patient monitor are

consistent with those displayed on the ventilator or anesthesia machine.

6. Re-configure the above parameters on the ventilatior or the anesthesia machine and

check if the parameter values displayed on the patient monitor change accordingly.

7. Trigger alarms [MV Too Low], [Airway Pressure Too High], [PAW Too High],

[Peak Too High], and [No Gas Supply] (no Air or O2) on the ventilatior or the

anesthesia machine. Check that these alarm messages are correctly recorded in the alarm

list of the patient monitor.

8. Switch the ventilator or anesthesia machine to volume control ventilation mode. Check

if the ventilation mode displayed on the patient monitor changes accordingly, and if the

parameter values of PEEP, Pmean, VTe, MV, I:E, and f(RR) are correctly displayed.

Serial Port Configuration List

External Device Setup Remark

If you need to view the parameters
of CO2、AG、BIS module in the

anesthesia machine, select

Mindray Wato 20/30/55/65 Not required.

[Factory Mainenance>>] →

[Function Configuration>>] →

[Select Module] in standby mode

and tick the corresponding module.

The following information is for

further reference:

Maquet Servo-i

Not required.

Maquet Servo-s

Baud Rate: 9600 bps

Word Length: 8 bits

Parity: even

Draeger Evita 2

Stop Bits: 1

Channel A: Not required;

Channel B:

Protocol: Medibus

/

Baud rate: 19200

Parity: even

Stop Bits: 1

3-40

External Device Setup Remark

Protocol: Medibus

Draeger Evita 2 dura/ Evita

4/ Evita XL

Newport E360 Protocol: Newport

Puritan Bennett 840

Hamilton G5（protocol
Polling）

Baud Rate: 19200

Parity: even

Stop Bits: 1

Interval: ---( Evita 2 dura)

Baud Rate: 38400

Word Length: 8 bits

Parity: NONE

Protocol: Polling.

/

The following information is for

further reference:

Baud Rate: 38400 bps

Word Length: 8 bits

Parity: NONE

Stop Bits: 1

/

The following information is for

further reference:

Baud Rate: 9600 bps

Word Length: 7 bits

Hamilton C2（protocol
Polling）

Hamilton Galileo（protocol
Polling）

Hamilton G5（protocol
Block）

Protocol: Polling.

Not required.

Protocol: Block.

Parity: even

Stop Bits: 2

The following information is for

further reference:

Baud Rate: 9600 bps

Word Length: 7 bits

Parity: even

Stop Bits: 2

The following information is for

further reference:

Baud Rate: 9600 bps

Word Length: 7 bits

Parity: even

Stop Bits: 2

The following information is for

further reference:

Baud Rate: 38400 bps

Word Length: 8 bits

3-41

Parity: none

Stop Bits: 1

External Device Setup Remark

The following information is for

further reference:

Ohmeda Avance/Aisys Not required.

Ohmeda Aestiva 7100

/7900

Drager Fabius GS/Plus/Tiro

Not required.

Protocol: Medibus

Baud Rate: 9600

Word Length: 7 bits

Parity: even

Stop Bits: 1

Protocol: Medibus

Baud Rate::9600

Baud Rate: 19200 bps

Word Length: 7 bits

Parity: odd

Stop Bits: 1

The following information is for

further reference:

Baud Rate: 19200 bps

Word Length: 7 bits

Parity: odd

Stop Bits: 1

/

Drager Primus

TCM CombiM/TCM

TOSCA

TOF-Watch SX Not required.

Word Length: 8 bits

Parity: even

Stop Bits: 1

Protocol: Monlink.

/

The following information is for

further reference:

Baud Rate: 9600 bps

Word Length: 8 bits

Parity: even

Stop Bits: 1

The following information is for

further reference:

Baud Rate: 19200 bps

Word Length: 8 bits

Parity: none

Stop Bits: 1

3-42

3.11.3 Installation and Test Report

Basic Information

Hospital Department

Serial number of ID

adapter

ID of the external device

Software version and other information of

the external device

Checking the connection

Can the patient monitor and the external device be assembled together using

designated accessories?

Does the green indicator of corresponding port on the BeneLink module illuminate

while the other indicators are not?

Are there numerics or characters displayed on the [Devices Integrated] screen of the

patient monitor?

Are the device type and parameter values displayed correctly on the [Devices

Integrated] screen of the patient monitor when the external device just enters working

mode?

Name of the external device

Type of serial port adapting

cable

Test Result
（Ye s /N o ）

Is the ventilation mode correctly displayed on the patient monitor? Does it change

correctly when the ventilation mode on the external device is changed?

Checking the parameters

Parameters on the external

device

PEEP PEEP

Pmean Pmean

VTe VTe

f ( RR ) f ( RR)

Ppeak Ppeak

Checking the alarms

Alarm

RR Too High

Apnea

Va lu e

Alarm messages displayed

on the external device

Parameters on the patient

monitor

Alarm messages displayed in the

alarm list of the patient monitor

Va lu e

Patient Disconnected

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Other information

3.12 Battery Check

Tools required:

 None.

Function Test

1. If the patient monitor is installed with batteries, remove the batteries first.

2. Verify that the patient monitor works correctly when running powered form an AC

source.

3. Insert two batteries per the procedures provided in the Operator’s Manual.

4. Remove the AC power cord and verify that the patient monitor still works correctly.

5. For T5 only: Remove one battery and verify that the patient monitor continues to work

correctly. Verify that the patient monitor can also work independently from another

battery.

Performance Test

Perform the test by referring to the Battery chapter in the Operator’s Manual and verify the

operating time of the battery meets the product specification.

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3.13 iView System Maintenance(for T8 and T9 monitors

only)

3.13.1 Making USB Startup Disk

Tools required:

 MakeUSB (PN: 110-002149-00)
 USB drive with capacity greater than 4G

1. Insert the USB drive into PC.

2. Run “prepareUSB.hta” file in the folder of MakeUSB.

3. Select [Prepare Windows PE USB Flash Drive] in the drop-down list, and select

[Next>].

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4. Select the drive label of the USB drive in the drop-down list, and configure [Format

USB-drive？]. [Select Ghost Image file to use] is unselected by default. Then select

[Next>].

5. Select [Prepare USB>] to start making the startup disk. The system selects [Full mode]

and [Manual mode] by default.

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6. Select [Close] to finish.

3.13.2 Restoring the System

Connecting the External USB Cable

Connect the iView maintenance USB disk which stores the system image files and keyboard

to the USB connectors special for iView maintenance.

Setting BIOS Screen

1. Start up the patient monitor and press [F2] key repeatedly on the keyboard.

2. Select [Main Menu] → [Maintenance>>] → [User Maintenance>>] → enter the

required password → [iView Maintenance>>] → [iView Maintenance], and when

the system switches to BIOS setup screen, stop press [F2] key.

3. Move the cursor to [Boot] by pressing [←] or [→] keys on the keyboard. Then press

[Enter] on the keyboard.

4. Move the cursor to [1st Boot], and press [Enter] on the keyboard.

5. Select [USB] and press [Enter] on the keyboard.

6. Move the cursor to [Save&Exit], and press [Enter] on the keyboard. Move the cursor to

[Yes] and press [Enter] on the keyboard to save the setup.

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Restoring the system

To recover the iView system, operate according to the following steps:

1. Start iView system, and press [F2] to enter BIOS. Select [Maintanence>>] → [User

Maitanence >>] → enter the required password → [iView Maitanence>>]→ [iView

Setup], and enter the following screen.

2. Select [Boot] in the menu bar, and then select option of [1st Boot] in the submenu. Press

enter key, and select [USB] in the popup window.

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3. Select [Save&Exit] in the menu bar. Then select the option of [Save Changes and Exit]

in the submenu and press [Enter] key. After that, select [Yes] to exit.

4. Insert the USB disk for iView maintanence (P/N: 115-017183-00) into the special USB

connector for iView system on the back housing of BeneView T8. The following screen

displays. Click the arrow, and the drop-down list will show. Select [Ghost image to

disk] from the list. Click [Next].

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5. Click [File] as shown in the below figure, and then choose the image file path of the

system. Click [OK]. Then select [Next].

3-50

6. Select [Run>], and start to recover the system with image files.

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7. The system recovery finishes.

Click [OK], and then click [Reboot]. When the monitoring screen of BeneView T8 displays,

remove iView maitanence USB disk. The system will restart and enter Windows 7 system. A

prompt to actiavate WIN7 will display.

8. Start the activation of Windows 7 system and enter the following screen.

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9. Input the key number.

3.13.3 Setting Automatic Login

iView system is set to be automatically logged in by default. However, if the registry is

modified, which leads to a manual login required, you can restore to the automatic login by

doing followings:

1. Select [Run] in the [Srart] menu of Windows system.

2. Input ‘regedit’ command, and then click [OK]. The [Registry Editor] window will pop

up.

3. In the [Registry Editor] window, find out the following three value entries by the path

of HKEY_LOCAL_MACHINE\SOFTWARE\Microsoft\Windows

NT\CurrentVersion\Winlogon. Check and change (if necessary) the value according to

what is shown below (the value is case sensitive).

 "AutoAdminLogon" = "1"

"DefaultUserName" =“CIS"

"DefaultPassword" =“MINDRAY"

If some value entry does not exist of the above listed three items, you have to create a
corresponding one: click the right button of mouse, select [New] → [String Value], and

input the string as the name of the new value entry, also input the correct value.

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3.14 Factory Maintenance

3.14.1 Accessing Factory Maintenance Menu

To access the factory maintenance menu, select [Main Menu]→ [Maintenance >>] →

[Factory Maintenance]and then enter the required password.

The [Factory Maintenance] menu is shown below.

3.14.2 Drawing Waves

There are two methods to draw waves: Color and Mono.

 Color: selecting Color will have smoother waveforms.
 Mono: selecting Mono will have a wider viewing angle.

3.14.3 Recorder

To enable/disable the recorder, select [Recorder] and toggle between [On] and [Off].

CAUTION

z The recorder is disabled if [Recorder] is switched off in the [Factory

Maintenance>>] menu.

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3.14.4 Software Version

Selecting [Software Version] will show software version information. The [Software

Version] menu is as follows:

3.14.5 Monitor Information

Selecting [Monitor Information] will show the status of the patient monitor. Monitor

information is displayed as follows:

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Maintenance and Test Report

(See the above sections for detailed test procedures and contents)

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

Test items Test records

Test

results(Pass/Fail)

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.

Power-on test

The power-on test is passed. The power indicator and alarm

system work correctly and the monitor start up properly.

Performance test

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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 [Ye s ]

The difference between the amplitude of the ECG calibration

square wave and that of the wave scale is not greater than 5%.

Resp test

The Resp wave is not distorted and the Resp value is within

40±2 rpm.

SpO2 test

Measure SpO2 on a healthy person’s finger and a Pleth wave

and PR value are displayed. The displayed SpO2 value is

within 95%-100%

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.

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.

C.O. test

The TB value displayed on the monitor is within 37±0.1ºC.

The displayed C.O. value is within 5±0.25L/min.

Mainstream CO2 test

The mainstream CO2 is zeroed successfully and the waveform

baseline recovers to zero.

CO2 Apnea alarm behaves correctly.

The displayed CO2 value is within 6±0.05％.

3-57

Sidestream CO2 test

Block the gas inlet of the module or watertrap. The sidestream

flowrate is slower than 10ml/min and an alarm of CO2

CO

2

Filterline Err is given. It indicates that there is no leakage.

The displayed CO2 value is within 6±0.05％.

Miscrostream CO2 test

Block the gas inlet of the module or watertrap. An alarm of

CO2 Filterline Err is given. It indicates that there is no leakage.

The displayed CO2 value is within 6±0.05％

AG test

When AG flowrate is slower than 10ml/min, an alarm of AG

Airway Occluded is given. It indicates that there is no leakage.

The fan inside the AG module works properly.

The measurement accuracy of CO2, N2O, O2 and AA (AA

represents an anaesthetic agent) meets the product

specifications in the Operator’s Manual.

ICG test

The measured results are as follows: HR=60±2 bpm,

VI=61±4/1000s, TFC=32±2/kOhms.

The measured results are as follows: HR=70±2 bpm, VI=48±4

/1000s, TFC=32±2 / kOhms.

BIS test (you can select either method to perform the test)

Method 1: The BIS value measured on healthy, wide-awake

adult is within 80-100.

Method 2: Connect to the BIS simulator to perform a cyclic

impedance check. The EEG wave and BIS numeric are

displayed on the monitor.

RM test

The displayed TV is within 500±50ml and RR is within

20±1rpm.

CCO/SvO2 test

The CCO/SvO2 numerics displayed on the patient monitor and

Vigilance monitor are consistent.

The waves (at the ECG signal output port) displayed on the

oscillograph are consistent with the ECG calibration waves

displayed on the monitor screen.

3-58

The amplitude of electrical level at the signal output port of

MAP, CVP and SpO

are 5±0.25V, 5±0.25V and 10±0.5V

2

respectively.

PiCCO test

The detected catheter type accords with the setting of the

Pulsion Calbox, and the measurement errors of TB and TI are
within ±0.1℃.

The displayed static pressure values of pArt and pCVP are no
more than (200±2) mmHg.

The waveforms of pArt and pCVP are displayed correctly.

ScvO2 test

The accuracy of ScvO2 measurements is (50±3)% and (80±

3)%.

NMT test

The measurement of [PK-PK] is between 54V and 66V. The

The measurement of [+Width] is between 270us to 330us.

The message “Test passed. The function of NMT sensor is

OK” is presented if sensor check completes successfully.

EEG test

The result of sensor check is pass, and EEG measurements are

displayed on the monitor.

Nurse call relay performance test

The relay contacts are close when an alarm occurs.

Analog output performance test

The waves displayed on the oscillograph are identical with

those displayed on the monitor.

Electrical safety tests

Refer to A Electrical Safety Inspection. All the electrical

safety tests should be passed.

Touchscreen calibration

The touchscreen is calibrated successfully.

Recorder check

The recorder can print ECG waves correctly and the printout is

clear.

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Set the recorder to some problems such as out of paper, paper

jam, etc. the monitor 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.

Network print test

The network printer can print out ECG reports correctly.

Device integration check

[Devices Integrated] window can display the type of the

external device, ventilation mode, and corresponding

parameters normally.

Battery check

The monitor can operates correctly from battery power when

an AC power failure accidentally occurs.

T5 patient monitor can operate independently on a single

battery.

The operating time of the battery meets the product

specification.

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4 Troubleshooting

4.1 Introduction

In this chapter, patient monitor problems are listed along with possible causes and

recommended corrective actions. Refer to the tables to check the patient monitor, identify and

eliminate the troubles.

The troubles 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.

4.2 Part Replacement

Printed circuit boards (PCBs), major parts and components in the patient monitor are

replaceable. Once you isolate a PCB you suspect defective, follow the instructions in 5
Repair and Disassembly to replace the PCB with a known good one and check that the

trouble disappears or the patient monitor passes all performance tests. If the trouble remains,

exchange the replacement PCB with the original suspicious PCB and continue

troubleshooting as directed in this chapter. Defective PCB can be sent to us for repair.

To obtain information on replacement parts or order them, refer to 6 Parts.

4.3 Patient Monitor Status Check

Some troubleshooting tasks may require you to identify the hardware version and status of

your patient monitor.

1. To view the information on system start time, self check, etc., select [Main Menu]→

[Maintenance >>]→[Monitor Information >>].

2. You can also view the information on the monitor’s current status by selecting [Main

Menu]→[Maintenance>>]→[Factory Maintenance>>]→enter the required password
→[Monitor Information >>].

4-1

4.4 Software Version Check

Some troubleshooting tasks may require you to identify the configuration and software

version of your patient monitor.

1. To view information on the system configuration and system software version, Select

[Main Menu]→[Maintenance>>]→[Software Version>>].

2. You can also view the information on system software version and module software

version by selecting [Main Menu]→[Maintenance>>]→[Factory Maintenance>>]→
enter the required password →[Software Version>>].

4.5 Technical Alarm Check

Before troubleshooting the patient 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 patient monitor’s

Operation Manual.

4.6 Troubleshooting Guide

4.6.1 Power On/Off Failures

Symptoms Possible Cause Corrective Action

The patient

monitor fails to

start. AC LED

or battery LED

does not light

AC mains not connected

or battery too low

Power supply protection Refer to 4.6.9 Power Supply Failures .

Cables defective or

poorly connected

Power switch & LED

board defective

Power module defective Replace the power module.

Mother board Defective Replace the mother board.

Check that AC mains is properly connected or

battery capacity is sufficient.

1. Check that the cables from power switch & LED

board to button board, button board to main board,

and power module to main board are correctly

connected.

2. Check that cables and connectors are not

damaged.

Replace the power switch & LED board.

4-2

4.6.2 Display Failures

Symptoms Possible Cause Corrective Action

Integrated display

is blank but the

patient monitor

still works

correctly.

Secondary display

does not function.

Secondary display

displays snows or

flashing specks

Cables defective or

poorly connected.

Backlight board

defective

Power module defective Replace the power module.

Display defective Replace the display.

Cables defective or

poorly connected.

DVI interface board

defective

Cables defective or

poorly connected.

1. Check that cables from the display to the mother

board and from the backlight board to the button

board/display are correctly connected.

2. Check that the cables and connectors are not

damaged.

Replace the backlight board.

1. Check that the cable between the display and the

patient monitor is correctly connected.

2. Check that the cables and connectors are not

damaged.

Replace the DVI interface board.

1. Check that the cable between the display and the

patient monitor is correctly connected.

2. Check that the cables and connectors are not

damaged.

overlapped or

distorted

Touchscreen does

not response

DVI interface board

defective

The mother board is

damaged.

FPGA error. Update or upgrade FPGA. Images

Cables defective or

poorly connected.

Touchscreen disabled

Replace the DVI interface board.

Replace the mother board.

1. Check that the cable between the display and

mother board is correctly connected.

2. Check that the cables and connectors are not

damaged.

Check if there is a symbol

[Main Menu] QuickKey. If yes, press the [Main

Menu] QuickKey for more than 3s to enable the

touchscreen.

shown above the

4-3

Cables defective or

poorly connected.

Touchscreen control

board defective

Button board defective. Replace the button board.

Touchscreen defective. Replace the touchscreen

Mother board defective Replace the mother board

Touch position

invalid

Touchscreen not

calibrated

4.6.3 Module Rack Failures

1. Check that the cables from the touchscreen to the

touchscreen control board, the touchscreen control

board to the button board, and the button board to

the mother board are correctly connected.

2. Check that the cables and connectors are properly

connected

Replace the touchscreen control board

Calibrate the touchscreen

Symptoms Possible Cause Corrective Action

SMR

SMR cannot

identify

parameter

modules

Extension Cable

defective or poorly

connected

Defective parameter

module

Wrong communication

board software revision

Module (in some slots)

unrecognized

1. Check that the cable between SMR and main unit

is properly connected

2. Check that the connecting cables and connectors

are not damaged.

3. Check that contact screws on SMR are tightly

screwed and properly contact the SMR.

Replace the suspicious parameter module with a

known good module. Check if the patient monitor

identifies the replacement module. If yes, it means

that the original one is defective.

Upgrade the program of the module or SMR.

1. Replace the Nios II module.

2. Replace the 8-slot module rack communication

board.

4-4

Power supply failure 1. Check if the voltage between two contact screws

in any slot reaches 12V DC. If yes and the

parameter module functions, the PCB assembly in

SRM might fail.

2. If there is no 12 V sent to the SMR, check that

the power module output voltage to the USB

interface board reaches 12V. If yes, the fuse on the

USB interface board might blow. Replace the USB

interface board.

Cable defective or

poorly connected

Nios II module loose or

failure

SMR interface board

failure

SMR communication

board failure

USB interface board

failure

Mother board failure Replace the mother board.

Integral module rack

Integral module

rack cannot

identify

parameter

modules

Module failure Replace parameter module. If a new module is

Cable defective or

poorly connected

1. Check that the cable between SMR interface

board and communication board is properly

connected.

2. Check that connecting cables and connectors are

not damaged.

1. Check that Nios II module is correctly plug ed

2. If the symptom persists, replace the Nios II

module.

Replace the SMR interface board.

Replace the SMR communication board.

Replace the USB interface board.

identified, the original one is defective.

1. Check that the cables from 3-slot module rack

communication board to MPM module rack

communication board, module rack to mother board

are properly connected.

Wrong communication

board software revision

Module (in some slots)

unrecognized

2. Check that connecting cables and connectors are

not damaged.

Upgrade the program of the module or Integral

module rack.

Replace the corresponding module rack

communication board.

4-5

Power supply to integral

module rack abnormal

3-slot or MPM module

rack communication

board failure

Nios II module failure Replace the Nios II module.

Mother board failure Replace the mother board.

1. Check if voltage between two contact screws in

any slot reaches 12VDC. If yes and the parameter

module functions, PCB assembly in the SMR might

fail.

2. If there is no 12V sent to the integrated module

rack, check that power module output voltage to

mother board reaches 12V DC. If yes, mother board

might fail.

Replace the 3-slot or MPM module rack

communication board.

4.6.4 Alarm Problems

Symptoms Possible Cause Corrective Action

The alarm lamp

is not light or

extinguished

but alarm

sound is issued

Cable defective or

poorly connected

1. Check that cables from alarm LED board to

button board and button board to mother board are

properly connected.

2. Check that connecting cables and connectors are

not damaged.

No alarm

sound is issued

but alarm lamp

is light

Alarm LED board

failure

Button board failure Replace the button board.

Mother board failure Replace the mother board.

Audio alarm disabled

Cable defective or

poorly connected

FPGA audio logic error Upgrade the audio logic part of the FPGA program.

Speaker failure Replace the speaker.

Replace the alarm LED board.

Select [Main Menu]→[Maintenance >>]→[User
Maintenance >>]→enter the required password→

[Alarm Setup >>], and then in the popup menu, set

[Minimum Alarm Volume] to appropriate setting.

In the [Others] window of the [Alarm Setup]

menu, set [Alm Volume] to appropriate setting.

1. Check that cable between speaker and mother

board is properly connected.

2. Check that connecting cables and connectors are

not damaged.

Mother board failure Replace the mother board.

4-6