Mindray h-6802-20-66855-beneviewt5-service-manual- TE5 Super Diagnostic Ultrasound System Service Manual (Advanced) Revision 18.0

BeneView T5
Patient Monitor
Service Manual
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called
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: 12.0 Release time: April 2016
© 2007-2016 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)
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........................................................... 2-8
2.3.4 Power Management System............................................................................. 2-10
2.3.5 Equipment Interface System ............................................................................ 2-12
2.4 Parameter Module ......................................................................................................... 2-14
2.4.1 Module Infrared Communication Board .......................................................... 2-14
2.4.2 Module Power Board ....................................................................................... 2-14
2.4.3 Module Button Board....................................................................................... 2-14
2.4.4 Parameter Board............................................................................................... 2-14
2.5 SMR .............................................................................................................................. 2-15
2.6 BeneLink Module.......................................................................................................... 2-16
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
Module Tests................................................ 3-7
2
1
3.4 Module Performance Tests ............................................................................................ 3-16
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 test ......................................................................................................... 3-32
3.5 Nurse Call Relay Performance Test .............................................................................. 3-33
3.6 Analog Output Performance Test .................................................................................. 3-33
3.7 Electrical Safety Test..................................................................................................... 3-34
3.8 Touchscreen Calibration................................................................................................ 3-34
3.9 Recorder Check............................................................................................................. 3-34
3.10 Network Print Test ...................................................................................................... 3-35
3.10.1 Equipment Connection and Setup.................................................................. 3-35
3.10.2 Print Function Test ......................................................................................... 3-35
3.11 BeneLink Module Check............................................................................................. 3-36
3.11.1 Device Connection and Setup ........................................................................ 3-36
3.11.2 Device Integration Function Test ................................................................... 3-38
3.11.3 Installation and Test Report............................................................................ 3-42
3.12 Battery Check.............................................................................................................. 3-43
3.13 Factory Maintenance................................................................................................... 3-44
3.13.1 Accessing Factory Maintenance Menu........................................................... 3-44
3.13.2 Drawing Waves .............................................................................................. 3-44
3.13.3 Recorder ......................................................................................................... 3-44
3.13.4 Software Version ............................................................................................ 3-45
3.13.5 Monitor Information....................................................................................... 3-45
4 Troubleshooting................................................................................................................ 4-1
4.1 Introduction..................................................................................................................... 4-1
4.2 Part Replacement ............................................................................................................4-1
4.3 Patient Monitor Status Check.......................................................................................... 4-1
4.4 Software Version Check .................................................................................................. 4-2
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 Output Interface Failures.................................................................................... 4-8
4.6.8 CF Card Problems.............................................................................................. 4-8
4.6.9 Power Supply Failures ....................................................................................... 4-9
4.6.10 Network Related Problems............................................................................. 4-10
4.6.11 Software Upgrade Problems............................................................................4-11
4.6.12 Technical Alarm Messages..............................................................................4-11
4.6.13 M51A Self Test Information............................................................................4-11
4.6.14 Device Integration Failures ............................................................................ 4-12
5 Repair and Disassembly ..................................................................................................5-1
5.1 Tools................................................................................................................................ 5-1
5.2 Preparations for Disassembly.......................................................................................... 5-1
5.3 Disassembling Procedure................................................................................................ 5-2
5.3.1 Removing the Recorder...................................................................................... 5-2
5.3.2 Separating the Front and Rear Housing ............................................................. 5-6
5.3.3 Removing the Power Switch & LED Board ...................................................... 5-8
5.3.4 Removing the Knob Encoder ............................................................................. 5-8
5.3.5 Removing the Button Board............................................................................... 5-9
5.3.6 Removing the Touchscreen Control Board ...................................................... 5-10
5.3.7 Removing the Inverter...................................................................................... 5-10
5.3.8 Removing the LCD ...........................................................................................5-11
5.3.9 Removing the Alarm LED Board..................................................................... 5-13
5.3.10 Removing the Fan Assembly.......................................................................... 5-13
5.3.11 Removing Battery Compartment Assembly................................................... 5-14
5.3.12 Removing the Integral Module Rack ............................................................. 5-15
5.3.13 Removing the CF Card Assembly.................................................................. 5-18
5.3.14 Removing the wireless AP assembly.............................................................. 5-19
5.3.15 Removing the Main Board ............................................................................. 5-21
5.3.16 Removing the Speaker ................................................................................... 5-23
5.3.17 Removing the Power Module Assembly ........................................................ 5-24
5.3.18 Removing the Main Support .......................................................................... 5-26
5.3.19 Removing the Interface Board Assembly....................................................... 5-26
5.4 Removing the SMR Assembly ...................................................................................... 5-29
5.5 Disassembling Modules ................................................................................................ 5-33
5.5.1 Disassembling the ICG Module ....................................................................... 5-33
5.5.2 Disassembling CO
Module ............................................................................. 5-37
2
3
5.5.3 Disassembling the BeneLink Module .............................................................. 5-43
5.5.4 Disassembling the New MPM Module ............................................................ 5-45
6 Parts ..................................................................................................................................6-1
6.1 Introduction..................................................................................................................... 6-1
6.2 Main Unit ........................................................................................................................ 6-2
6.2.1 Exploded View ................................................................................................... 6-2
6.2.2 Parts List ............................................................................................................ 6-2
6.3 Front housing Assembly.................................................................................................. 6-3
6.3.1 12.1” LCD with Anti-glare Screen..................................................................... 6-3
6.3.2 12.1” LCD with Touchscreen ............................................................................. 6-4
6.3.3 12.1” Screen Assembly (with anti-glare screen) ................................................ 6-6
6.3.4 12.1” Screen Assembly (with touchscreen)........................................................ 6-7
6.4 Main Unit ........................................................................................................................ 6-8
6.4.1 Main Unit Assembly .......................................................................................... 6-8
6.4.2 Battery Compartment Assembly ...................................................................... 6-10
6.4.3 Power Module assembly ...................................................................................6-11
6.4.4 Interface Board Assembly ................................................................................ 6-12
6.4.5 Main Board Assembly...................................................................................... 6-15
6.4.6 Integral module rack ........................................................................................ 6-16
6.4.7 Main Support Assembly................................................................................... 6-17
6.4.8 Rear Housing Assembly................................................................................... 6-18
6.4.9 CF Card Assembly ........................................................................................... 6-19
6.4.10 6802 Internal Wireless AP Assembly ............................................................. 6-21
6.5 SMR .............................................................................................................................. 6-22
6.5.1 SMR Assembly................................................................................................. 6-22
6.5.2 SMR Inside Assembly...................................................................................... 6-23
6.6 Parameter Modules........................................................................................................ 6-25
6.6.1 MPM Module................................................................................................... 6-25
6.6.2 New MPM Module .......................................................................................... 6-26
6.7 Remote Display Box ..................................................................................................... 6-28
6.8 New Wireless AP Package (ASUS) for 6800/6802 ....................................................... 6-30
6.9 Replaceable Parts .......................................................................................................... 6-31
6.9.1 Main Unit ......................................................................................................... 6-31
6.9.2 SMR ................................................................................................................. 6-33
6.9.3 Parameter Modules........................................................................................... 6-34
7 Upgrade............................................................................................................................. 7-1
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.............................................................. 7-5
7.3.3 Upgrading Recorder ........................................................................................... 7-5
4
7.3.4 Upgrading Analog Output.................................................................................. 7-5
7.3.5 Upgrading CF storage card function .................................................................. 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 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 cu rrent
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).
CIS 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).
The patient monitor also:
), oxygen (O2), anesthetic gas (AG), impedance cardiograph (ICG),
2
), electroencephalograph (EEG), and neuromuscular
2
, pulse rate (PR),
2
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 Not using screw and bracket specified by Mindray may cause the screw to touch
the internal battery and lead to monitor damage (the proper screw depth should be between 6.5mm and 7.5mm). Take out the rubber stoppers in the two screw holes of the base when installing the tray.
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. Analog Output and Defibrillator Connector: It is a Micro-D connector used to output
analog signals and defibrillator synchronization signals.
4. CIS Connector: It is used to connect a CIS.
5. Video Output: It is a DVI-D connector used to connect a secondary display.
6. Auxi Output Connector: It is a BNC connector used to output nurse call signals.
7. Network Connector: It is a RJ45 connector used to connect an ethernet network or a PC.
8. USB Connector: used to connect any USB-compatible peripheral device.
9. SMR Connector: It is used to connect the SMR and outputs a 12V DC.
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 and speaker Processing and communications system: main board and integral module rack assembly. Power management system: battery, battery interface board and power module Equipment interface system: USB_Hub 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 Alarm LED board Inverter
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. The signals and power supply from 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 alarm lamp
signals are transferred by the button board and are directly controlled by the main board
Recorder
The recorder receives data 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 (It is
ON during normal working) on its front panel. It is connected with the mother board.
The following diagram shows its operating principle.
2-6
Module Description
Power interface Introduces a DC from the main board.
Recorder power
module
Recorder CPU Controls 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.
Controls the communications between the main board and the recorder
CPU.
Receives the control signals from the CPU and then forwards them to the
step motors
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.
2-7
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.
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.
2-8
The mother board is in charge of connections and communications with other components
and provides the following interfaces:
Name Description
LCD connector Connects the built-in display.
Video output +IO +IIC Connects the digital video interface board.
USB×2+network+RS422
+GPIO port
Button board connector Connects the button board.
Recorder connector Connects the recorder.
CF card connector Connects the CF card assembly.
Speaker connector Connects the speaker.
Power module connector Connects the power module.
Integral module rack connector
Fan connector Connects the fan.
Internal wireless network card
assembly
Connects the USB_Hub board.
Connects the 3-slot rack communication board in the integral
module rack.
Connects the internal wireless network card.
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 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.
2-9
2.3.4 Power Management System
Battery
The patient monitor uses two chargeable lithium-ion batteries (11.1 V, 4500 mAh). The
battery compartment is located at the bottom of the patient monitor. The battery power is
supplied to the mother board via the battery interface board, and then to the power module.
Battery Interface Board
The Battery interface board connects the batteries to the DC input terminal of the power
module via the mother board, implementing charging and discharging of 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 charging & power management board, voltage
drop DC transforming board and voltage rise and drop DC transforming board.
The power module converts the input power into DC power supplies and then distributes
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.
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 3
DC outputs:
Outputs Description
3.3 V
5.0 V
Power supply of the LCD, mother board, CPU board, DVI interface
board and integral module rack.
Power supply of the DVI interface board, recorder, CF storage card
board and USB_Hub board.
12 V
Power supply of the recorder, LCD inverter, integral module rack, parameter modules, USB_Hub board
2-10
The following diagram shows the pins of the power socket connecting the power module and
the mother board:
Pin ID Marking Description
1/3/5 12V The positive output of the 12 VDC power
2/4/6/8/10/
27/28/29/30
7/9 3V3 The positive output of the 3.3 VDC power
11 5V The positive output of the 5 VDC power
12 BC1 Signal indicating whether battery 1 is available. Low level indicates
13/15 BAT+1 Input of battery 1, connecting to the positive pole of the battery.
14 NTC1 Thermistor signal of battery 1.
16 BC2 Signal indicating whether battery 2 is available. Low level indicates
18 NTC2 Thermistor signal of battery 2.
17/19 BAT+2 Input of battery 2, connecting to the positive pole of the battery.
20 PCON Power on/off control signal. It is a TTL pulse signal inputted from
GND The output grounding terminal of the power board.
that battery 1 is available and high level indicates that battery 1 is
not available.
that battery 2 is available and high level indicates that battery 2 is
not available.
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, 2 s
for power off and 10 s for illegal power off.
21 BCON Backlight on/off signal and switch output signal. The main board
sends the LCD backlight on/off signals to the power board via a
serial port, the power board processes the signals and output them.
Low level is output when the backlight is off and high level is
output when the backlight is on.
22 LED-BAT Battery status indication driving output
23 LED-AC AC power status indication signal
24 LCD-BR Backlight brightness control voltage.
2-11
2.3.5 Equipment Interface System
USB_Hub board
The USB_Hub board is connected with the mother board. It is compatible with USB1.1
connectors and supports equipment hot plug. The UART signal output by the main board is
converted into RS422 signal by the USB_HUB board. It receives 5 VDC and 12 VDC inputs
from the power module, of which the 5 VDC is supplied to the USB interface board and the
12 VDC is outputted to the SMR connector through a fuse.
BNC It is a BNC connector used to output nurse call signals.
RJ 45 connector
USB connector Connects devices with USB connector.
USB&POWER
connector
It is a standard RJ45 connector, providing 10/100 BASE-TX Ethernet
communications channels. It connects an Ethernet network or a PC.
Provides RS232 and RS422 interfaces for the communication between main
board and SMR. It receives 5 VDC and 12 VDC inputs from the power
module, of which the 5 VDC is supplied to the USB interface board and the
12 VDC is outputted to the SMR connector through a fuse.
2-12
DVI Interface Board
The DVI interface board is connected with the mother board. The following diagram shows
its interfaces to other components.
Interface Description
DVI connector Connects the secondary display.
CIS Connector Connects the CIS system.
Micro-D connector Outputs analog signals and defibrillator synchronization signals.
CF Card Assembly
The CF assembly serves the non-volatile CF card which is used for data storage and
transferring. 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.
2-13
2.4 Parameter Module
Each parameter module may consist 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 Module Button Board
There are keys and a LED on the module button board.
2.4.4 Parameter Board
The parameter board is a parameter measurement component, which is the most important
component of the parameter module.
2-14
2.5 SMR
The satellite module rack (SMR) is independent of the patient monitor. It 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 supply. It is run by 12 V DC supplied by the patient
monitor and then supplies power supply to each parameter module via the contact
screws.
It implements communication 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.
2-15
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
patient monitor
BeneView
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
CPU
module
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
2-16
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 after 3
2
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 CO
2
] 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 CO
2
] menu, enter 6% (the CO
2
] menu, the measured CO2 concentration is displayed. After the
2
concentration) in the [CO
2
] to calibrate the
2
] field.
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 passwordModule 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 ; delta impedance as 0.5 , 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 SpO
connector of the monitor. Set [Patient Cat.] to [Adu]
2
and [PR Source] to SpO2 on the monitor.
2. Measure SpO
on your finger. (Assume that you stay healthy)
2
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
sensor from your finger and make sure that an alarm of SpO2 Sensor
2
Off is triggered.
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 1354.9 (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
k
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 stopcoc
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 ‘125040000’ (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 ScvO
2
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.
3-34
3.7 Electrical Safety Test
See A Electrical Safety Inspection for electrical safety tests.
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 [Scr een 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.
3-35
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
3.10.1 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
SNDF5042AFBE 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)
SNDA5031AFCFsupport
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
Serial number of ID
adapter
ID of the external device
Software version and other information of
Department
Name of the external device
Type of serial port adapting
cable
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?
Test Result Yes/No
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
Value
PEEP PEEP
Pmean Pmean
VTe VTe
f ( RR ) f ( RR)
Parameters on the patient
Value
monitor
Ppeak Ppeak
Checking the alarms
Alarm
Alarm messages displayed on the external device
Alarm messages displayed in the
alarm list of the patient monitor
RR Too High
Apnea
Patient Disconnected
3-43
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.
3-44
3.13 Factory Maintenance
3.13.1 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.
3.13.2 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.
3.13.3 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.
3-45
3.13.4 Software Version
Selecting [Software Version] will show software version information. The [Software Version] menu is as follows:
3.13.5 Monitor Information
Selecting [Monitor Information] will show the status of the patient monitor. Monitor
information is displayed as follows:
3-46
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
3-47
ECG performance test
ECG waves are displayed correctly without noise and the HR
value is within 80±1 bpm.
ECG Lead Off alarm behaves correctly.
Paced signals are detected and pace pulse marks are displayed
when [Paced] is set to [Yes]
The difference between the amplitude of the ECG calibration
square wave and that of the wave scale is not greater than 5%.
Resp test
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%.
3-48
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.
3-49
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 TOF-Ratio is between 79 and 81.
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.
3-50
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.
3-51
FOR YOUR NOTES
3-52
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 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 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
Display defective Replace the display.
Cables defective
or poorly
connected.
DVI interface
board defective
Cables defective
or poorly
connected.
1. Check that the cable from the display to the
mother board and the cables from the backlight
board respectively to the button board and the
display are correctly connected.
2. Check that the cables and connectors are not
damaged.
Replace the backlight board.
Replace the power module.
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.
distorted
Touchscreen does not
response
DVI interface
board defective
The mother board
is damaged.
FPGA error. Update or upgrade FPGA. Images overlapped or
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.
4-3
shown above the
Cables defective
or poorly
connected.
Touchscreen
control board
defective
Button board
defective.
Touchscreen
defective.
Mother board
defective
Touch position invalid Touchscreen not
calibrated
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
Replace the button board.
Replace the touchscreen
Replace the mother board
Calibrate the touchscreen
4.6.3 Module Rack Failures
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
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.
Module (in some
slots) not recognized
Replace the Nios II module.
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 properly and the PCB assembly in
SRM might fail.
2. If there is no 12 VDC power sent to the SMR, check
whether the power voltage output to the USB_Hub
board by the power module reaches 12V. If yes, the
fuse of the USB interface board might blow. Replace
the USB_Hub board.
Cable defective or
poorly connected
Nios II module loose
or failure
SMR interface board
failure
SMR communication
board failure
USB_Hub 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_Hub 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
Alarm LED board failure Replace the alarm LED board.
Button board failure Replace the button board.
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
Mother board failure Replace the mother board.
Select [Main Menu][Maintenance >>][User Maintenance >>]enter the required password
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.
Mother board failure Replace the mother board.
[Alarm Setup >>], and then in the popup menu, set [Minimum Alarm VolumeAlm Sound] to appropriate setting.[On] 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.
4-6
4.6.5 Button and Knob Failures
Symptoms Possible Cause Corrective Action
Buttons do not
work
Knob does not
work
Cable defective or
poorly connected
Button board failure Replace button board.
Cable defective or
poorly connected
Knob failure Replace the knob encoder.
Button board failure Replace the button board
1. Check that cable between button board and
mother board is properly connected.
2. Check that connecting cables and connectors are
not damaged.
1. Check that cables from knob to button board, and
button board to mother board are properly
connected
2. Check that connecting cables and connectors are
undamaged.
4.6.6 Recorder Failures
Symptoms Possible Cause Corrective Action
No printout
Recorder module
disabled
1. Check if the recorder status LED lights
2. If yes, enable the module in [Factory Maintenance] menu. Otherwise, check for other
possible causes.
Poor print quality
or paper not
feeding properly
Paper reversed Re-install the paper roll.
Cable defective or
poorly connected
Recorder power
supply failure
Recorder failure Replace the recorder.
Paper roll not
properly installed
Print head dirty 1. Check the thermal print head and the paper roller
Print head failure Replace the print head.
Recorder failure Replace recorder.
1. Check that cable between recorder and mother
board is properly connected.
2. Check that connecting cables and connectors are
not damaged.
Check if the power module outputs 5 V DC and 12V
DC correctly.
Stop the recorder and re-install the paper roll.
for foreign matter.
2. Clean the thermal print head with an appropriate
clean solution.
4-7
4.6.7 Output Interface Failures
Symptoms Possible Cause Corrective Action
No analog signals or
nurse call signals are
issued
Device with USB port
does not function
(Assume that the
peripheral devices are
good)
Respective output
disabled
USB_Hub board cable
loose
USB_Hub board failure Replace the USB_Hub board.
Mother board failure Replace the mother board.
Cable defective or
poorly connected
USB_Hub board failure Replace the USB_Hub board.
Mother board failure Replace the mother board.
1. Select [Main Menu][Analog Output Setup]set [Analog Output] to [On].
1. Check that cable between USB_Hub
board and mother board is properly
connected.
2. Check that connecting cables and
connectors are not damaged.
1. Check that cable between USB_Hub
board and mother board is properly
connected.
2. Check that connecting cables and
connectors are not damaged.
4.6.8 CF Card Problems
Symptoms Possible Cause Corrective Action
CF card malfunctions
Wrong CF card or small
memory space
CF card full; data error;
CF card error
CF card failure Replace the CF card.
Cable defective or
poorly connected
CF card board failure Replace the CF card board.
Mother board failure Replace the mother board.
Use only SanDisk-manufactured CF storage
cards. Those with 1GB memory space are
recommended.
Format CF card on PC.
1. Check that the cable between CF card
board and mother board is correctly
connected.
2. Check that connecting cables and
connectors not damaged.
4-8
4.6.9 Power Supply Failures
Symptoms Possible Cause Corrective Action
Different battery
voltages
Battery capacity is too
low
Battery cannot be
recharged
Battery failure Replace battery.
Cable defective or
poorly connected
Power board failure Replace the power board.
Battery failure Replace battery.
Cable defective or
poorly connected
Power board failure Replace the power board.
Battery failure Replace battery and recharge the replacement
Cable defective or
poorly connected
1. Check that the cable between battery
interface board and power module is
correctly connected.
2. Check that cables and connectors are not
damaged.
1. Check that the cable is correctly
connected.
2. Check that connecting cables and
connectors are not damaged.
battery. If the replacement battery can be
recharged, the original one fails.
1. Check that cable between battery interface
board and power module is correctly
connected.
No +3.3 V output
No +5.0 V output
No +12 V output
2. Check that cables and connectors are not
damaged.
Power board failure Replace power board
1. Power supply
protected
2. Power board failure
1. Turn off the patient monitor then restart it.
2. If the problem remains, disconnect the AC
mains for 5 s and reconnect it, then restart
the patient monitor.
3. If the problem still remains, replace the
power board.
4-9
NOTE
z When the power module has a failure, it may cause problems to other components,
e.g. the monitor suddenly breaks down during start-up, as the power module may have a power supply protection. In this case, troubleshoot the power module per the procedure described in the table above.
z Components of the main unit, SMR and parameter modules are powered by the
power module. In the event that a component malfunctions, check if the operating voltage is correct. Refer to 2 Theory of Operation for the operating voltage and measurement points of each comp onent.
4.6.10 Network Related Problems
Symptoms Possible Cause Corrective Action
Frequent dropouts and
network disconnects
The patient monitor is
connected to a LAN
but cannot view other
patients in the View
Others mode
Incorrect LAN cable
connection
Incorrect IP address
configuration
Incorrect LAN cable
connection
Excessive requests for
viewing the patient
monitor at the same time
Incorrect IP
configuration
USB_Hub board failure Replace the USB_Hub board.
Check LAN cable connection. LAN cable
shall not be longer than 50 m.
Check for IP address conflict. Reconfigure IP
address.
Check LAN cable connection. LAN cable
shall not be longer than 50m.
A patient monitor can only be viewed by 4
other patient monitors at the same time under
the View Others mode. The excessive view
requests system will be ignored.
Check for IP address conflict. Reconfigure IP
address.
4-10
4.6.11 Software Upgrade Problems
Symptoms Possible Cause Corrective Action
Bootstrap upgrade
fails
Program upgrade fails
Power failure or
unintended power off
during bootstrap upgrade
Incorrect network
connection
Wrong upgrade package
has been downloaded
Incorrect IP address
configuration
Return the CPU board to factory for repair.
1. Check that network connector, not iView
connector, on the patient monitor is used.
2. Make sure that the hub or switch run
normally. Check that net twines are of the
right type and have been connected
correctly.
Upgrade package shall be .pkg files. Select
package according to system requirement.
Configure a fixed IP address in range C as
specified for the patient monitor. We
recommend not to upgrade a program when
the patient monitor is connected to a network
with multiple PCs.
4.6.12 Technical Alarm Messages
Please refer to the Operator’s manual.
4.6.13 M51A Self Test Information
New MPM module applies the integrative parameter board (ECG ASIC).
MPM Selftest Item Test Value
DSP selftest
information
7024 selftest
information
2131 selftest
information
ECG module selftest
information
Not F
Not 7F
Not 1F
Normal value7 for 3/5
lead module; FF for
12-lead module
Test Value (New MPM module)
Not FF Replace the module
Corrective Action
4-11
4.6.14 Device Integration Failures
Symptoms Possible Cause Corrective Action
1. Replace the ID adapter.
The [Devices Integrated]
window displays
nothing after
connection.
Generate the alarm:
[BeneLink Comm Stop].
The patient monitor
has no response
when loading the
ID adapter.
The ID adapter is not
compatible with the
external device.
The serial port adapting
cable is not compatible with
the external device.
Wrong software version or
wrong protocol version of
the external device.
The application of the
BeneLink module is
damaged.
The application of the
BeneLink module is
damaged.
The kernel or the document
system of the BeneLink
module is damaged.
2. Upgrade the ID adapter in [Factory Maintenance] menu to make the ID
adapter match the corresponding external
device. See 3.11.1 Device Connection and Setup for more about the setup of the ID.
Replace the serial port adapting cable.
Make sure the protocol version and software
version are supported by the BeneLink
module.
Update or upgrade the application of the
BeneLink module with the network
upgrading tool.
Update or upgrade the application of the
BeneLink module with the network
upgrading tool.
Return the BeneLink module to factory for
repair.
4-12
5 Repair and Disassembly
5.1 Tools
During disassembly and replacing, the following tools may be required:
Phillips screwdrivers Small flat-bladed screwdrivers Contact spanner Tweezers Sharp nose pliers Sleeve
5.2 Preparations for Disassembly
Before disassembling the monitor, finish the following preparations:
Stop monitoring the patient, turn off the monitor and disconnect all the accessories and
peripheral devices.
Disconnect the AC power source and take out both of the batteries. Pull off all the modules in the integral module rack. If the SMR is connected, disconnect
the SMR from the monitor and then remove all the modules in it.
WARNING
z Before disassembling the monitor, be sure to eliminate the static charges first.
When disassembling the parts labeled with static-sensitive symbols, make sure you are wearing electrostatic discharge protection such as antistatic wristband or gloves to avoid damaging the equipment.
z Put the cables or wires in place when reassemble the monitor to avoid short circuit. z When assembling the monitor, be sure to select proper screws. If an unfit screw is
tightened by force, the monitor may be damaged and the screw or the part may fall off during use to cause unpredictable damage or human injury.
z Be sure to follow the correct sequence to disassembly the monitor. Otherwise, the
monitor may be damaged permanently.
z Be sure to disconnect all the cables before disassembling any parts. Be sure not to
damage any cables or connectors.
z Be sure to place the monitor face up when disassembling it. Otherwise, the screen
or the knob may be scratched or damaged.
5-1
5.3 Disassembling Procedure
5.3.1 Removing the Recorder
1. Open the recorder door and unscrew the two M3×6 screws.
2. Pull the two clips in the directions as indicated and meanwhile pull out the recorder.
NOTE
z Be sure not to damage the connecting cables or connectors when pulling out the
recorder.
5-2
3. Unscrew the M3×6 screw and unplug the recorder grounding cable and the cable
between the recorder and the mother board.
4. Pull the two clips backwards and remove the recorder driving board.
5-3
5. Pull the press bar upwards about 1 mm and then unplug the flexible cable. Remove the
cable that connects the driving board and the button board. Unscrew the PT2×6 screw
and remove the drive board’s grounding cable. Then take out the recorder driving board.
6. Unscrew the two PT2×6 screws and take out recorder’s button board.
5-4
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