PM-9000 Service Manual

PM-9000 Super
Patient Monitor
Service Manual
Intellectual Property Statement
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray)

owns the intellectual property rights to this product and this manual. This manual may refer to
information protected by copyrights or patents and does not convey any license under the
patent rights of Mindray, nor the rights of others. Mindray does not assume any liability arising
out of any infringements of patents or other rights of third parties.
Mindray intends to maintain the contents of this manual as confidential information. Disclosure
of the information in this manual in any manner whatsoever without the written permission of
Mindray is strictly forbidden. Release, amendment, reproduction, distribution, rent, adaption
and translation of this manual in any manner whatsoever without the written permission of
Mindray is strictly forbidden.
and are the registered trademarks or trademarks owned by Mindray in

China and other countries. All other trademarks that appear in this manual are used only for
editorial purposes without the intention of improperly using them. They are the property of their
respective owners.
Contents of this manual are subject to changes without prior notice.
For this Service Manual, the issued Date is January 2006 (Version: 2.0).
© 2002-2006 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.
I
Manufacturer’
s Responsibility
All information contained in this manual is believed to be correct. Mindray shall not be liable for
errors contained herein nor for incidental or consequential damages in connection with the
furnishing, performance, or use of this manual.
Mindray is responsible for safety, reliability and performance of this product only in the
condition that:
n all installation operations, expansions, changes, modifications and repairs of this
product are conducted by Mindray authorized personnel; and,
n the electrical installation of the relevant room complies with the applicable
national and local requirements; and,
n this product is operated under strict observance of this manual.
Warranty
This warranty is exclusive and is in lieu of all other warranties, expressed or implied, including
warranties of merchantability or fitness for any particular purpose.
Exemptions
Mindray's obligation or liability under this warranty does not include any transportation or other
charges or liability for direct, indirect or consequential damages or delay resulting from the
improper use or application of the product or the use of parts or accessories not approved by
Mindray or repairs by people other than Mindray authorized personnel.
This warranty shall not extend to

n any Mindray product which has been subjected to misuse, negligence or
accident; or
n any Mindray product from which Mindray's original serial number tag or product
identification markings have been altered or removed; or
n any product of any other manufacturer.
II
Return Policy
In the event that it becomes necessary to return a unit to Mindray, follow the instructions below.
1. Obtain a return authorization.

Contact the Mindray Service Department and obtain a Mindray Customer Service
Authorization Number. The Mindray Customer Service Authorization Number must appear on
the outside of the shipping container. Return shipments will not be accepted if the Mindray
Customer Service Authorization Number is not clearly visible. Please provide the model
number, serial number, and a brief description of the reason for return.
2. Freight policy
The customer is responsible for freight charges when this product is shipped to Mindray for
service (including any relevant customs fees or other freight related charges).
3. Return address
Please send the part(s) or equipment to the address offered by Customer Service Department.
III
Contact Information
Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Address: Mindray Building, Keji 12th Road South, Hi-tech Industrial Park,
Nanshan, Shenzhen 518057 P.R. China
Tel: +86 755 26522479 +86 755 26582888
Fax: +86 755 26582500 +86 755 26582501
Website: www.mindray.com.cn
EC Representative: Shanghai International Holding Corp. GmbH (Europe)
Address: Eiffestraße 80, 20537 Hamburg Germany
Tel: 0049-40-2513175
Fax: 0049-40-255726
IV
Safety Precautions
1. Meaning of Signal Words
In this manual, the signal words DANGER, WARNING, and CAUTION are used
regarding safety and other important instructions. The signal words and their meanings are
defined as follows. Please understand their meanings clearly before reading this manual.
Signal word Meaning
Indicates an imminently hazardous situation which, if not

DANGER avoided, will result in death or serious injury.
Indicates a potentially hazardous situation which, if not

WARNING avoided, could result in death or serious injury.
Indicates a potentially hazardous situation which, if not

CAUTION avoided, may result in minor or moderate injury.
2. Meaning of Safety Symbols

Symbol Description
Type-BF applied part
"Attention" (Refer to the operation manual.)
Safety Precautions
Please observe the following precautions to ensure the safety of service engineers as well as
operators when using this system.
DANGER: Do not use flammable gases such as anesthetics, or flammable
liquids such as ethanol, near this product, because there is danger of

explosion.
WARNING: Do not connect this system to outlets with the same circuit breakers
and fuses that control current to devices such as life-support

systems. If this system malfunctions and generates an over
current, or when there is an instantaneous current at power ON, the
circuit breakers and fuses of the building’s supply circuit may be
tripped.
V
CAUTION: 1. Malfunctions due to radio waves
(1) Use of radio-wave-emitting devices in the proximity of this kind

of medical electronic system may interfere with its operation.
Do not bring or use devices which generate radio waves, such
as cellular telephones, transceivers, and radio controlled toys,
in the room where the system is installed.
(2) If a user brings a device which generates radio waves near the
system, they must be instructed to immediately turn OFF the
device. This is necessary to ensure the proper operation of
the system.
2. Do not allow fluids such as water to contact the system or

peripheral devices. Electric shock may result.
VI
Symbols
Be Careful Protective earth ground
Indicates that the instrument is IEC-60601-1 Type CF equipment. The unit

displaying this symbol contains an F-Type isolated (floating) patient applied part providing
a high degree of protection against shock, and is suitable for use during defibrillation.
Equipotential grounding terminal CE mark 93/42/EEC a directive

of the European Economic Community
Silence Symbol ！ Close all alarm volume
@ Mark Event 》 Next menu
*** Highest level alarm ** Middle level alarm
* Lowest level alarm Alarm pause
Ð Trend graph cursor u SYS pressure（NIBP trend graph）
t DIA pressure(NIBP trend graph) * MEAN pressure (NIBP trend graph)
Î Right moving indicator Í Left moving indicator
Heart beat Pace signal
× Gain magnify √ Confirm
SN Series Number
VII
FOR YOUR NOTES
VIII
Contents
Contents
CHAPTER 1 ABOUT THE PRODUCT.................................................................................................1
1.1 INTRODUCTION ...............................................................................................................................1

1.2 APPLICATION ...................................................................................................................................1
1.3 ENVIRONMENT................................................................................................................................3
CHAPTER 2 PRINCIPLES......................................................................................................................1
2.1 GENERAL ........................................................................................................................................1

2.2 HARDWARE D ESCRIPTION ..............................................................................................................3
2.3 SOFTWARE D ESCRIPTION............................................................................................................. 13
2.4 S YSTEM PARAMETER ................................................................................................................... 15
CHAPTER 3 PRODUCT SPECIFICATIONS ......................................................................................1
3.1 SAFETY C LASSIFICATIONS ...............................................................................................................1

3.2 ENVIRONMENTAL SPECIFICATIONS ..................................................................................................2
3.3 P OWER S OURCE SPECIFICATIONS ....................................................................................................3
3.4 HARDWARE SPECIFICATIONS ...........................................................................................................4
3.5 WIRELESS NETWORK .......................................................................................................................5
3.6 DATA STORAGE ................................................................................................................................5
3.7 SIGNAL OUTPUT SPECIFICATIONS ..................................................................................................6
3.8 ECG SPECIFICATIONS .....................................................................................................................7
3.9 RESP S PECIFICATIONS .....................................................................................................................9
3.10 SP O2 SPECIFICATIONS .................................................................................................................. 10
3.11 IBP SPECIFICATIONS .................................................................................................................... 12
3.12 TEMP SPECIFICATIONS ................................................................................................................ 13
3.13 IBP SPECIFICATIONS..................................................................................................................... 13
3.14 CO S PECIFICATIONS ..................................................................................................................... 14
3.15 CO2 SPECIFICATIONS .................................................................................................................... 15
3.16 AG SPECIFICATIONS ..................................................................................................................... 18
CHAPTER 4 DISASSEMBLING/ASSEMBLING & TROUBLESHOOTING ..................................1
4.1 PM-9000 EXPRESS DISASSEMBLING/ASSEMBLING ......................................................................1

4.2 TROUBLESHOOTING .......................................................................................................................6
CHAPTER 5 TEST AND MATERIAL LIST .........................................................................................1
5.1 TEST PROCEDURE .........................................................................................................................1

5.2 NIBP CALIBRATION........................................................................................................................5
5.3 IBP CALIBRATE ..........................................................................................................................5
5.4 CO2 CHECK .................................................................................................................................8
5.5 AG CALIBRATE..........................................................................................................................9
5.6 PM-9000 EXPRESS MATERIAL LIST .............................................................................................11
I
Contents
CHAPTER 6 MAINTENANCE AND CLEANING.................................................................................1
6.1 MAINTENANCE ...............................................................................................................................1

6.2 CLEANING .......................................................................................................................................1
6.3 CLEANING R EAGENT ......................................................................................................................1
6.4 STERILIZATION ................................................................................................................................2
6.5 DISINFECTION .................................................................................................................................2
II
About the Product
Chapter 1 About the Product
1.1 Introduction
The PM-9000 Super Patient Monitor, a portable and accessible patient monitor, is supplied by
rechargeable batteries or external AC power, which applies to adults, pediatric and neonates.
You can select different configurations as required. Besides, the PM-9000 Super can be
connected with the central monitoring system whereby a monitoring network will be formed.
Parameters that the PM-9000 Super can monitor include: ECG, RESP, SpO2, NIBP, 2-channel
TEMP, 2-channel IBP, CO and CO2. It, integrating the functions of parameter measurement,
waveform monitoring, freezing and recording, is a compact and lightweight patient monitor. Its
color TFT LCD is able to show patient parameters and 8 waveforms clearly. The compact
control panel and knob control, and the easy-to-use menu system enable you to freeze, record,
or perform other operations conveniently.
The PM-9000 Super measures patient’
s ECG, NIBP, SpO2, TEMP, RESP, IBP, CO and CO2
physiological signals through the ECG electrode, SpO2 sensor, cuff, temperature sensor and
pressure transducer. During the measurement, the patient monitor does not get energy or any
substance from the human body, and does not release any substance to the human body.
However, it releases sine wave signals to the patient when measuring the respiration rate. The
patient monitor converts the measured physiological signals to the digital signals, waveforms
and values, and then displays them on the screen. You can control the patient monitor through
the control panel. For example, you can set different alarm limits for different patients. Thus,
when the patient monitor detects any physiological parameter exceeding the preset alarm limit,
it will enable the audio and visual alarm.
1.2 Application
1.2.1 General
In the treatment processes, it is necessary to monitor important physiological information of
patients. Therefore, the patient monitor has been playing an outstanding role among medical
devices. The development of technology does not only help medical staff get the important
physiological information, but also simplifies the procedures and makes it more effective. For
patients in hospital, the basic and important physiological information is required, including
ECG, SpO2, RESP, IBP, CO, CO2, TEMP, etc. In recent years, the development of science and
technology helping measure and get important physiological information of patients has made
the patient monitor more comprehensive in performance and better in quality. Today,
multi-parameter patient monitors are widely used.
1.2.2 Usage
Parameters that the PM-9000 Super can monitor include: ECG, RESP, SpO2, NIBP, TEMP, IBP,
CO AGand CO2. The PM-9000 Super converts these physiological signals to digital signals,
processes them and displays them on the screen. You can set the alarm limit as required.
1-1
About the Product
When the monitored parameter exceeds the preset alarm limit, the patient monitor will start the
alarm function. In addition, you can control the patient monitor through the control panel.
Usually, patient monitors are seen in some clinical areas in hospital, such as ICU, CCU,
intensive care units for heart disease patients, operating rooms, emergency departments and
observation wards. They can also be used in clinics. The PM-9000 Super should be run under
the control of clinical staff.
PM-9000 Super patient monitor has the following functions:

Heart Rate (HR)
ECG
2-channel ECG waveform
Arrhythmia analysis and S-T analysis (optional)
Respiration Rate (RR)
RESP
Respiration waveform
Pulse Oxygen Saturation(SpO2), Pulse Rate (PR)
SpO2
SpO2 Plethysmogram
Systolic pressure (NS), diastolic pressure (ND), mean pressure
NIBP
(NM)
T1, T2, TD
TEMP
CH1: SYS, DIA

IBP
CH2: SYS, DIA
IBP waveform
Temperature of blood (TB)
CO
Cardiac Output (CO)
End-tidal carbon dioxide (EtCO2)
CO2
Inspired minimum CO2 (InsCO2)
Airway Respiration Rate (AwRR)
Inhaled and exhaled CO2 (FiCO2, EtCO2)
AG
Inhaled and exhaled N2O (FiN2O, EtN2O)
Inhaled and exhaled O2 (FiO2, EtO2)
Inhaled and exhaled anesthetic agent (FiAA, EtAA, where AA
refers to any of the following anesthetic agents.)
HAL (Halothane)
ISO (Isoflurane)
ENF (Enflurane)
SEV (Sevoflurane)
DES (desflurane)
Airway Respiration Rate (rpm: Respiration Per Minute): AwRR
Minimum Alveolar Concentration (MAC)
4 AG waveforms (CO2, N2O, O2, AA)
The PM-9000 Super provides the functions of audio/visual alarm, trend graphic storage and
output, NIBP measurement, alarm event identification, large font screen, defibrillator
synchronization, oxyCRG recall, drug calculation, etc.
1-2
About the Product
1.3 Environment
1.3.1 Temperature
Work mode 0 – 40℃
MINDRAY CO2 module +5 – +35℃
Welch Allyn mainstream CO2 module +10 – +40℃
Microstream CO2 module +5 – +35℃
Artema AION AG module +10 – +35℃
Transportation & Storage -20 – 60℃
1.3.2 Humidity
Work mode 15% – 95 % (non-condensing)
Transportation & Storage 10% – 95 % (non-condensing)
Atmospheric pressure 70.0kPa – 106.0kPa
1.3.3 Electrical specification

100 – 240 V AC, 50/60 Hz,
Maximum input power: 140VA; fuse: T 3A
2.3 Ah 12V lead-acid rechargeable battery
Working time of fully-charged batteries in normal status: 120 minutes (2 batteries).
From the first low-battery alarm, the batteries can supply power to the patient monitor for 5
more minutes.
Maximum charging time: =12h
4.4Ah 11.1V lithium battery

Working time of fully-charged batteries in normal status: 300 minutes (2 batteries).
From the first low-battery alarm, the batteries can supply power to the patient monitor for 5
more minutes.
Maximum charging time: = 6.5h
1-3
About the Product
FOR YOUR NOTES
1-4
Principles
Chapter 2 Principles
2.1 General
The intended use of the patient monitor is to monitor a fixed set of parameters including ECG,
RESP, SpO2, NIBP, TEMP, IBP, CO and CO2 (IBP, CO and CO2 are optional). It consists of the
following functional parts:
Parameter measurement;
Main control part;
Man-machine interface;
Power supply;
Other auxiliary functions;
These functional units are respectively detailed below.
Figure 2-1 Structure of the PM-9000 Super
2.1.1 Parameter Measurement

The parameter measurement and monitoring are the core functions of the patient monitor. The
parameter measurement part of the patient monitor consists of the measurement probe,
2-1
Principles
parameter input socket assembly, NIBP assembly and the main control board.
This part converts the physiological signals to electric signals, processes the those signals and
conducts the calculation by the preset program or command delivered from the main control
board, and then sends the values, waveforms and alarm information (which will be displayed
by using the man-machine interface) to the main control board.
2.1.2 Main Control Part

In the PM-9000 Super, the main control part refers to the main control part of the main control
board. It drives the man-machine interface, manages the parameter measurement and
provides users with other special functions, such as storage, recall of waveforms and data.
(See Figure 2-1)
2.1.3 Man-Machine Interface

The man-machine interface of the patient monitor includes the TFT display, recorder, speaker,
indicator, buttons and control knob.
The TFT display is the main output interface. It, with the high resolution, provides users with
abundant real-time and history data and waveforms as well as various information and alarm
information.
The recorder is a subsidiary of the display, which is used for the user to print data.
The speaker provides the auditory alarm function.
The indicator provides additional information about the power supply, alarms and so on.
The buttons and control knob are the input interface, which are used for the user to input the
information and commands to the patient monitor.
2.1.4 Power Supply

The power supply part is an important part of the patient monitor. It includes the main power
PCB, backlight board, batteries and fan.
The main power PCB converts the external AC current respectively to the 5V DC and 12V DC
current, which are supplied for the whole system. For the TFT display, there is a special
requirement on the power supply, so a backlight board is used. The batteries supply power for
the system for a short time when there is no external AC current. The fan is used for the heat
sink of the system.
2.1.5 Other Auxiliary Functions

The patient monitor also provides the network upgrade function for the service engineers to
upgrade the system software without disassembling the enclosure.
2-2
Principles
2.2 Hardware Description

The structure of the patient monitor is shown in the following figure.
Figure 2-2 Functional structure of the PM-9000 Super
The PM-9000 Super PCB connection is shown in the following figure.
Figure 2-3 PCB connection
2-3
Principles
Basic functions and working principles of modules are described in the following sections.
2.2.1 Main Board
2.2.1.1 General
The main board is the heart of the patient monitor. It implements a series of tasks, including the
system control, system scheduling, system management, data processing, file management,
display processing, printing management, data storage, system diagnosis and alarm.
2.2.1.2 Principle diagram
Figure 2-4 Working principle of the main board
2.2.1.3 Principle
The main board is connected with external ports, including the power input port, multi-way
serial port, TFT display interface, analog VGA interface, network port and analog output port.
Besides, on the main board is also a BDM interface reserved for the software debugging and
software downloading.
CPU System
CPU is the core part of the main board. It, connected with other peripheral modules
through the bus and I/O cable, implements the data communication, data processing,
logical control and other functions.
RTC
RTC provides the calendar information (such as second, minute, hour, day, month and
year). CPU can read and modify the calendar information from RTC.
Ethernet Controller
Ethernet Controller supports the IEEE802.3/IEEE802.3u LAN standard, and supports two
data transmission rate: 10Mbps and 100Mbps. CPU exchanges data with the Ethernet
through the Ethernet Controller.
Analog Output
2-4
Principles
The D/A converter converts the digital ECG/IBP signals sent from CPU to the analog
signals, which are provided for the external after low-pass filtered by the filter and
amplified by the amplifier.
FPGA and VRAM
VRAM stores the displayed data. CPU stores the displayed data to VRAM through FPGA.
FPGA gets data from VRAM, processes them, and then sends them to the relevant
graphic display device.
In addition, FPGA also extends multiple serial ports, which communicate with peripheral
modules. FPGA transfers the received data to CPU through the bus; CPU delivers data to
FPGA through the bus, and then the FPGA transfers those data to the peripheral
modules.
Watchdog
When powered on, watchdog provides reset signals for CPU, FPGA and Ethernet
Controller.
The patient monitor provides the watchdog timer output and voltage detection functions.
2.2.2 ECG/RESP/TEMP Module
2.2.2.1 General
This module provides the function of measuring three parameters: electrocardiograph (ECG),
respiration (RESP) and temperature (TEMP).
Figure 2-5 Working principle of the ECG/RESP/TEMP module
2.2.2.3 Principle
This module collects the ECG, RESP and TEMP signals through the transducer, processes the
signals, and sends the data to the main board through the serial port.
ECG Signal Input Circuit
The input protection and filtering circuits receive the ECG signal from the transducer, and filter
the high-frequency interference signal to protect the circuit against the damage by defibrillator
high-voltage and ESD.
2-5
Principles
The right-leg drive circuit gets the 50/60Hz power common-mode signal from the lead cable,
and sends the negative feedback signal to the human body to reject the common-mode
interference signal on the lead cable, which helps the detection of the ECG signal.
The lead-off detecting circuit checks whether the ECG lead is off, and sends the information to
CPU.
ECG Signal Process Circuit
The difference amplifying circuit conducts the primary amplification of the ECG signal and
rejects the common-mode interference signal.
The low-pas filtering circuit filters the high-frequency interference signal beyond the frequency
band of the ECG signal.
The PACE signal refers to the ECG pace signal. It has significant interference to the ECG
signal detection. The PACE rejection circuit can rejects the PACE signal, which helps the ECG
signal detection.
The main amplifying/filtering circuit conducts the secondary amplification of the ECG signal,
filters the signal, and then sends the ECG signal to the A/D conversion part.
Pace Detect
This part detects the PACE signal from the ECG signal and sends it to CPU.
Temperature Detect Circuit
This circuit receives the signal from the temperature transducer, amplifies and filters it, and
then sends it to the A/D conversion part.
Carrier Generate Circuit
The RESP measurement is based on the impedance method. While a man is breathing, the
action of the breast leads to changes of the thoracic impedance, which modulates the
amplitude of the high-frequency carrier signal. Finally, the modulated signal is sent to the
measurement circuit. The purpose of this module is generating the high-frequency carrier.
RESP Signal Input Circuit
This circuit couples the RESP signal to the detecting circuit.
RESP Signal Process Circuit
The pre-amplifying circuit conducts the primary amplification of the RESP signal and filters it.
The detecting circuit detects the RESP wave that has been modulated on the actuating signal.
The level shifting circuit removes the DC component from the RESP signal.
The main amplifying/filtering circuit conducts the secondary amplification of the RESP signal,
filters the signal, and then sends it to the A/D conversion part.
A/D
The A/D conversion part converts the analog signal to the digital signal, and sends the signal
to CPU for further processing.
CPU System
n Implementing the logical control of all parameter parts and A/D conversion parts;
n Implementing the data processing for all parameters;
n Implementing the communication with the main board.
Power & Signal isolate Circuit
n Isolating the external circuits to ensure the safety of human body;
n Supplying power for all circuits;
n Implementing the isolation communication between the CPU System and the main board.
2-6
Principles
2.2.3 CO/IBP Module
2.2.3.1 General
This module provides the function of measuring two parameters: Cardiac Output (CO) and
Invasive Blood Pressure (IBP).
Figure 2-6 Working principle of the CO/IBP module
2.2.3.3 Principle
This module collects the CO/IBP signal through the transducers, processes it and sends it
to the main board throgh the serial port.
CO Signal Process Network
The CO parameter is measured with the thermal dilution method. The transducer
sends two signals (TI: Temperature of Injectate; TB: Temperature of Blood) to the CO
Signal Process Network. After that, the signals are amplified and low-pass filtered, and
then sent to the CPU System for processing.
IBP Signal Process Network
The IBP signal is the differential signal. After the common-mode filtering, the difference
signal is amplified by the difference amplifying circuit which changes the dual-end signal
to the single-end signal. After the low-pass filtering, the IBP signal is sent to the CPU
System for processing.
CPU System
n Converting the analog signal obtained by the circuit to the digital signal;
n Implementing the logical control of all parameter parts;
n Implementing the data processing for the two parameters;
n Implementing the isolation communication between the CPU System and the main
board.
2-7
Principles
2.2.4 SpO2 Module
2.2.4.1 General
This module provides the function of measuring the Pulse Oxygen Saturation (SPO2).
Figure2-7 Working principle of the SpO2 module
2.2.4.3 Principle
The SpO2 measurement principle
1. Collecting the light signal of the red light and infrared transmitting through the finger
or toe which is pulsing;
2. Processing the collected signal to get the measured result.
The drive circuit of the LED and the gain of the amplifying circuit should be controlled
according to the different perfusions and transmittances of the tested object.
Led Drive Circuit
This circuit supplies the LED with the drive current, which can be regulated.
SPO2 Signal Process Network
The pre-amplifying circuit converts the photoelectric signal to the voltage signal and conducts
the primary amplification.
The gain adjusting and amplifying circuit conducts the secondary signal amplification and
adjusts the gain.
The biasing circuit adjusts the dynamic range of the signal, and sends it to the A/D conversion
part.
A/D
The A/D conversion part converts the analog signal to the digital signal, and then sends it to
CPU for further processing.
D/A
The D/A conversion part converts the digital signal received from CPU to the analog signal,
and provides the control signal for the Led Drive Circuit and SPO2 Signal Process Network.
CPU System
2-8
Principles
n Implementing the logical control of all the circuits;

n Implementing the data processing for the SpO2 parameter;
n Implementing the isolation communication between the CPU System and the main
board.
2.2.5 NIBP Module
2.2.5.1 General
This module provides the function of measuring the Non-Invasive Blood Pressure (NIBP)
parameter.
Figure 2-8 Working principle of the NIBP module
2.2.5.3 Principle
The NIBP is measured based on the pulse vibration principle. Inflate the cuff which is on the
forearm till the cuff pressure blocks the arterial blood, and then deflate the cuff according to a
specified algorithm. While the cuff pressure is decreasing, the arterial blood has pulses, which
are sensed by the pressure transducer in the cuff. Consequently, the pressure transducer,
connected with the windpipe of the cuff, generates a pulsation signal, which is then processed
by the NIBP module to get the NIBP value.
Valve Drive Circuit
This circuit controls the status (ON/OFF) of valves. It, together with the Motor Drive Circuit,
implements the inflation and deflation of the cuff.
2-9
Principles
Motor Drive Circuit

This circuit controls the action of the air pump. It, together with the Valve Drive Circuit,
implements the inflation and deflation of the cuff. Besides, it provides the status signal of the
motor for the A/D conversion part.
NIBP Signal Process Network
The NIBP signal is the differential input signal. The difference amplifying circuit amplifies the
dual-end difference signal and converts it to the single-end signal; meanwhile, this circuit
sends a channel of signal to the A/D conversion part, and the other to the DC isolating and
amplifying circuit.
The DC isolating and amplifying circuit removes DC components from the signal, amplifies the
signal, and then sends it to the A/D conversion part.
A/D
The A/D conversion part converts the analog signal to the digital signal, and sends it to the
CPU System for further processing.
Over Pressure Detect
The circuit detects the NIBP pressure signal. Once the pressure value exceeds the protected
pressure value, it will send a message to the CPU System, which asks the Valve Drive Circuit
to open the valve to deflate the cuff.
CPU System
n Implementing the logical control of all the circuits;
n Implementing the data processing for the NIBP parameter;
2.2.6 Recorder Module
2.2.6.1 General
This module is used to drive the heat-sensitive printer.
Figure 2-9 Working principle of the recorder module
2.2.6.3 Principle
This module receives the to-be-printed data from the main board, converts them to the dot
2-10
Principles
matrix data, sends them to the heat-sensitive printer, and drives the printer.
Step Motor Drive Circuit
There is a step motor on the heat-sensitive printer. The step motor drives the paper. This
circuit is used to drive the step motor.
Printer Status Detect Circuit
This circuit detects the status of the heat-sensitive printer, and sends the status information to
the CPU system. The status information includes the position of the paper roller, status of the
heat-sensitive recorder paper and the temperature of the heat-sensitive head.
CPU System
n Processing the data to be printed;
n Controlling the heat-sensitive printer and step motor;
n Collecting data about the status of the heat-sensitive printer, and controlling the
printer;
2.2.7 Button Panel
2.2.7.1 General
This module provides a man-machine interactive interface.
Figure 2-10 Working principle of the button panel
2.2.7.3 Principle
This module detects the input signals of the button panel and control knob, converts the
detected input signals to codes and then sends to the main board. The main board sends
commands to the button panel, which, according to the commands, controls the status of the
LED and the audio process circuit to give auditory/visual alarms.
CPU
n Detecting the input signal of the button panel and control knob;
n Controlling the status of LED;
2-11
Principles
n Controlling the audio process circuit;

n Regularly resetting the Watchdog timer;
n Communicating with the main board.
Audio Process Circuit
This circuit generates audio signals and drives the speaker.
Watchdog
When powered on, the Watchdog provides the reset signal for CPU.
The patient monitor provides the watchdog timer output and voltage detection functions.
2.2.8 Power PCB
2.2.8.1 General
This module provides DC working current for other boards.
Figure 2-11 Working principle of the power PCB
2.2.8.3 Principle
This module can convert 220V AC or the battery voltage to 5V DC and 12V DC voltages, which
are supplied for other boards. When the AC voltage and batteries coexist, the AC voltage is
supplied for the system and used to charge the batteries.
AC/DC
This part converts the AC voltage to the low DC voltage for the subsequent circuits; besides, it
supplies the power for charging the batteries.
Battery Control Circuit
When the AC voltage and batteries coexist, this circuit controls the process of charging the
batteries with the DC voltage converted by the AC/DC part. When the AC voltage is
unavailable, this circuit controls the batteries to supply power for the subsequent circuits.
5V DC/DC
This part converts the DC voltage to the stable 5V DC voltage and supplies it for the external
boards.
2-12
Principles
12V DC/DC
This part converts the DC voltage to the stable 12V DC voltage and supplies it for the external
boards.
Power Switch Circuit
This circuit controls the status of the 5V DC/DC part and the 12V DC/DC part, thus to control
the switch of the patient monitor.
Voltage Detect Circuit
This circuit detects the output voltages of the circuits, converts the analog signal to the digital
signal, and sends the digital signal to the main board for processing.
2.3 Software Description
2.3.1 General
Figure 2-12 System function
As shown in Figure 2-12, in the red frame is the software system, on the left to the red
frame are the inputs of the software system, and on the right to the red frame are the
outputs. The parameter measurement module exchanges data with the software through
the serial port, while the user interacts with the system through the button panel. Among
the output devices, the recorder and alarm device receive data through the serial ports,
the analog output component is an MBUS component, and the LCD and network
controller are controlled directly by CPU.
2-13
Principles
2.3.2 System Task

NO Task Function Period
In case of a
1 System initialization Initializing the system
startup
2 Data processing Analyzing and saving the data 1 second
Display of timer
3 Implementing the timed refreshing 1 second
information
In case of a
Switchover of modules Switching over between waveforms and
5 screen change
and screens parameters on the screen
event
Processing of user
Processing the user inputs by buttons and In case of a
6 commands and
displaying them on the screen. button event
screens
System monitoring, voltage monitoring and
7 System monitoring 1 second
battery management
8 Network connection Implementing the network connection 1 second
9 Network data sending Sending the network data 1 second
10 Network data receiving Receiving the network data (viewbed) 1 second
Analyzing ECG signal, calculating ECG values
11 ECG analysis (HR, ARR and ST), and saving the analysis 1 second
results.
In case of a
12 Record output Outputting records
record event
13 NIBP processing Implementing NIBP-related processing 1 second
14 WATCHDOG task Managing the system watchdog 1 second
2-14
Principles
2.3.3 System Function

The system tasks can be classified as follows.
Figure 2-13 System task
2.4 System Parameter
2.4.1 General
For the PM-9000 Super patient monitor, signals are collected by modules, and the results are
2-15
Principles
transferred to the main board through the adapter board, thus to process and display the data
and waveforms. Commands from the main board, as well as the status information of modules,
are transferred through the adapter board. In addition, the adapter board adapts and changes
the power supply. The structure of the whole system is shown in the following figure.
---
As shown in Figure 2-14, the five modules and measurement cables monitor and measure
NIBP, SpO2, ECG/RESP/TEMP, IBP/CO and CO2 in real time, and send the results to the main
board for processing and displaying. If necessary, the results are sent to the recorder for
printing.
The parameter monitoring functions are described respectively in the following sections.
2.4.2 ECG/RESP
■　 ECG
The PM-9000 Super patient monitor has the following ECG functions:
1) Lead type: 3-lead, 5-lead, 12-lead
2) Lead way:
3-lead (1 channel): I, II, III
5-lead (2 channels): I, II, III, aVR, aVL, aVF, V
12-lead (8 channels): I, II, III, aVR, aVL, aVF, V1-V6, CAL
3) Floating input
4) Right-foot drive
5) Lead-off detection
6) 2-channel ECG waveform amplification; processing ECG signals of any two leads
■　 The ECG circuit processes the ECG signals. It consists of the following parts:
2-16
Principles
1) Input circuit: The input circuit protects the ECG input level, and filters the ECG signals
and external interference. The ECG electrode is connected to the input circuit through the
cable.
2) Buffer amplifying circuit: This circuit ensures extremely high input impedance and low
output resistance for ECG.
3) Right-foot drive circuit: The output midpoint of the buffer amplifying circuit is fed to the
RL end of the 5-lead after the inverse amplification, so as to ensure that the human body
is in the equipotential state, decrease the interference, and increase the common-mode
rejection ratio of the circuit.
4) Lead-off detection: The lead-off causes changes in the output level of the buffer
amplifying circuit. Therefore, the lead-off can be detected with a comparator, and the state
of lead-off can be converted TTL level for the Micro Controller Unit (MCU) to detect it.
5) Lead circuit: Under the control of MCU, the lead electrodes should be connected to the
main amplification circuit.
6) Main amplification circuit: The measurement amplifier is composed of 3 standard
operation amplifiers.
7) Subsequent processing circuit: This circuit couples the ECG signals, remotely controls
the gains, filters the waves, shifts the level, amplifies the signal to the specified amplitude,
and sends the signal to the A/D converter.
■　 RESP
The PM-9000 Super measures the RESP based on the impedance principle. While a man
is breathing, the action of the breast leads to impedance changes between RL and LL.
Change the high-frequency signal passing the RL and LL to amplitude-modulation
high-frequency signal (AM high-frequency signal), which is converted to the electric signal
after being detected and amplified and then sent to the A/D converter. The RESP module
consists of the RESP circuit board and coupling transformer. The circuit has several
functions: vibration, coupling, wave-detection, primary amplification and high-gain
amplification.
2.4.3 NIBP
The NIBP is measured based on the pulse vibration principle. Inflate the cuff which is
on the forearm till the cuff pressure blocks the arterial blood, and then deflate the cuff
according to a specified algorithm. While the cuff pressure is decreasing, the arterial
blood has pulses, which are sensed by the pressure transducer in the cuff.
Consequently, the pressure transducer, connected with the windpipe of the cuff,
generates a pulsation signal. Then, the pulsation signal is filtered by a high-pass filter
(about 1Hz), amplified, converted to the digital signal by the A/D converter, and finally
processed by the MCU. After that, the systolic pressure, diastolic pressure and mean
pressure can be obtained. For neonates, pediatric and adults, it is necessary to select
the cuffs of a proper size to avoid possible measurement errors. In the NIBP
measurement, there is a protection circuit used to protect patient from over-high
pressure.
The NIBP measurement modes include:
1) Adult/pediatric/neonate mode: To be selected according to the build, weight and age
2-17
Principles
of the patient;
2) Manual/Auto/Continuous mode: The manual measurement is also called single
measurement; in this mode, only one measurement is done after being started. In the
auto measurement mode, the measurement can be done once within the selected
period, with the interval being 1, 2, 3, 4, 5, 10, 15, 30, 60, 90, 120, 180, 240 or 480
minutes. In the continuous measurement mode, quick continuous measurement will be
done within 5 minutes after being started; it detects the changes in blood pressure
effectively.
2.4.4 SpO2
The SpO2 value is obtained through the pulse waves of the finger tips based on specific
algorithm and clinical data. The SpO2 probe is the measurement transducer. It has two
inbuilt LEDs and an inbuilt light receiver. The two LEDs include one red-light diode and
one infrared diode, which emit light in turns. When the capillaries in the finger tip are
iteratively congested with blood pumped by the heart, the light emitted by the LEDs, after
absorbed by the capillaries and tissue, casts on the light receiver, which can sense, in the
form of electric signal, the light strength changing with the pulsated blood. The DC/AC
ratio of the two photoelectric signals corresponds to the content of the oxygen in the blood.
Therefore, the correct pulse oxygen saturation can be obtained with specific algorithm.
Moreover, the pulse rate can be obtained according to the pulse waveform.
The circuit of the SpO2 module is involved in four parts: SpO2 probe, signal processing
unit, LED-driven sequencing control part and the MCU.
2.4.5 TEMP
Temperature measurement principle:
1. The transducer converts the body temperature to the electric signal;
2. The amplifier amplifies the electric signal;
3. The CPU processes the data.
The circuit is a proportional amplifier consisting of operation amplifiers. When the
temperature reaches the heat-sensitive probe, the heat-sensitive probe generates the
voltage signal, which is sent to the A/D converter after being amplified. The probe
detecting circuit is a voltage comparator consisting of operation amplifiers. When the
probe is disconnected, the voltage input is lower than the comparing voltage, so the
voltage comparator outputs the low level; when the probe is connected, the voltage input
is higher than the comparing voltage, so the voltage comparator outputs the high level.
2.4.6 IBP
The IBP module can monitor the arterial pressure, central venous pressure and
pulmonary arterial pressure.
Measurement principle: Introduce a catheter, of which the external end is connected to
the pressure transducer, into the blood vessel under test, inject the physiological saline.
Since the liquid can be transferred by pressure, the pressure inside the blood pressure is
transferred by liquid to the pressure transducer, and the dynamic waveform of the
pressure inside the blood pressure is obtained in real time. Thus, the arterial pressure,
central venous pressure and pulmonary arterial pressure are obtained based on specific
2-18
Principles
algorithm.
2.4.7 CO
CO measurement principle: The thermal dilution method is widely used in the clinical CO
monitoring. Introduce a floating catheter into the pulmonary artery through the right atrium,
and inject the physiological saline into the right atrium through the catheter whose front
end is connected to the temperature transducer. When the cold liquid mixes with the
blood, there will be a change of temperature. Thus, when the blood mixed with the
physiological saline flows into the pulmonary artery, its temperature will be sensed by the
temperature transducer. According to the injection time and temperature change, the
patient monitor can analyze the CO, and calculate the Cardiac Index (CI), Stroke Volume
Index (SVI), SVIs of the left atrium and right atrium, Pulmonary Vascular Resistance (PVR)
and so on.
2.4.8 CO2
The CO2 module works based on the infrared spectrum absorption principle. According to
different connection methods, the infrared light transducer is classified as the mainstream
infrared light transducer and sidestream infrared light transducer. The sidestream CO2
module is composed of the circuit board, inbuilt sidestream infrared light transducer,
deflation pump and control. When used, this module requires the external water trap,
drying pipe and sampling tube. The mainstream CO2 module is composed of the circuit
board and external mainstream infrared light transducer. The infrared light transducer
needs to be preheated. In the sidestream mode, the deflation rate can be set to
100ml/min, 150ml/min or 200ml/min according to the patient situation. In the AG
monitoring, multiple compensations can be set, such as hydrosphere, oxygen,
temperature and desflurane (Des). When the CO2 measurement is not being conducted,
the sidestream deflation pump, the transducer of the mainstream module, and the infrared
source are expected to be shut down, thus to extend the service life and reduce the power
consumption of the module. In the mainstream mode, the infrared light transducer takes a
longer time to be preheated, and there is no windpipe which is available in the sidestream
mode.
2.4.9 AG
The Anesthesia Gas (AG) can be used to measure the AG and respiration gas of the
anesthetized patient. The AG concentration is measured based on the principle that the
AG has the property of absorbing the infrared. All gases that the AG module can measure
have the property of absorbing the infrared, and every gas has their own specific
absorption peculiarity.
AG measurement procedure:
1. Send the gas to be measured to a sampling chamber;
2. Use an optical infrared filter, select a specific band of infrared, and transmit it
through the gas;
3. Measure the infrared that gets through the gas to obtain the gas concentration.
For a given volume, the higher the gas concentration is, the more absorbed infrared is,
and the less the infrared that gets through the gas is. For the measurement of multiple
2-19
Principles
gases, multiple infrared filters are required in the AG module.

The oxygen does not absorb the infrared within the above-mentioned wave band.
Therefore, the oxygen is measured based on its paramagnetism. Inside the transducer of
the O2 module, there are two crystal balls full of nitrogen. They are suspended in the
symmetrical magnetic field, and designed to point to the strongest outgoing part of the
magnetic field. Outside the balls is the paramagnetic oxygen. Therefore, the balls are
forced, by the relatively stronger paramagnetic oxygen, out of the magnetic field. The
moment of the force acting on the balls is proportional to the paramagnetic strength as
well as to the concentration of the paramagnetic oxygen.
2-20
Product Specifications
Chapter 3 Product Specifications
3.1 Safety Classifications
Class I with internal electric power supply.

Type of protection against Where the integrity of the external protective earth (ground) in
electric shock the installation or its conductors is in doubt, the equipment shall
be operated from its internal electric power supply (batteries)
Monitor: B
Degree of protection Sidestream CO2/AG: BF (defibrillation proof)
against electric shock ECG/RESP/TEMP/SpO2/NIBP/IBP/
CO/mainstream CO2: CF (defibrillation proof)
Degree of protection
against hazards of ignition
Not protected (ordinary)
of flammable anesthetic
mixtures
Degree of protection
against harmful ingress of Not protected (ordinary)
water
Mode of operation Continuous
Equipment type Portable
3-1
3.2 Environmental Specifications
0 to 40℃
5 to 35℃ (With Mindray CO2 module)
Operating temperature 10 to 40℃ (With Welch Allyn CO2 module)
5 to 35℃ (With Oridion CO2 module)
10 to 35℃ (With AION AG module)
Operating humidity 15 to 95%, noncondensing
-500 to 4600m (-1640 to 15092 feet)

Altitude -305 to 3014m (-1000 to 9889 feet) (with CO2, AG, Masimo or
Nellcor SpO2 module)
Storage temperature –20 to 60℃
Storage humidity 10 to 95%, noncondensing
3-2
3.3 Power Source Specifications
AC mains
Input voltage 100 to 240V
Frequency 50/60Hz
Power 140VA
Fuse T 3A
Internal battery
Number of batteries 2
Type Sealed lead-acid battery or lithium-ion battery
Time to shutdown 5 to 15min (after the first low-power alarm)
Sealed lead-acid battery
Nominal voltage 12VDC
Capacity 2.3Ah
48 minutes or 120 minutes typical when powered by one or two

Operating time new fully-charged batteries respectively (25℃, ECG, SpO2,
NIBP measurement per 15 minutes).
A maximum of 6 h for each battery, and a maximum of 12h for

Charge time
both (in the running status or standby mode)
Lithium battery
Rated voltage 11.1VDC
Capacity 4.4Ah
120 minutes or 300 minutes typical when powered by one or two

Operating time new fully-charged batteries respectively (25℃, ECG, SpO2,
NIBP measurement per 15 minutes).
Charge time A maximum of 6.5h (in the running status or standby mode)
3-3
3.4 Hardware Specifications
Physical
Size 318 × 270 × 137mm (width×height×depth)
Different due to different configurations

Weight Standard configuration: 4.7kg
Maximum weight: = 7.5kg
Display
Type Color TFT LCD
Size 10.4 inches (diagonal)
Resolution 800×600 pixels
Recorder
Type Thermal dot array
Horizontal resolution 160 dots/cm (at 25 mm/s recording rate)
Vertical resolution 80 dots/cm
Width of the recorder paper 50 mm
Length of the recorder paper 30 m
Recording rate 25 mm/s, 50 mm/s
Recorded waveforms 2
LED indicator
Alarm indicator 1 (yellow and red)
AC power indicator 1 (green)
Audio indicator
Giving audio alarms, keypad tones, and heartbeat/pulse tone.

Speaker Supporting PITCH TONE and multi-level volume.
Audio alarms comply with EN475 and IEC60601-1-8.
Control
1 knob, which can be rotated clockwise/counterclockwise or

Control knob
pressed.
Button 7 buttons: POWER, MAIN, FREEZE, PAUSE, RECORD,
3-4
NIBP, MENU
Connectors
Power supply 1 AC power connector
Parameter ECG, RESP, TEMP, SPO2, NIBP, IBP, CO, CO2, AG
Network 1 standard RJ45 network connector, 100 BASE-TX
VGA 1 standard color VGA monitor connector, 15-PIN D-sub
Auxiliary output 1 BNC connector
Equipotentiality 1 equipotential grounding connector
3.5 Wireless network
Standards IEEE 802.11b, Wi-Fi compatible
Frequenct range 2.412 to 2.462GHz
China America Canada Europe Spain France Japan
Operating channel 1 to 11 10, 11 2
For other country, please refer to your local law.
Safe distance 10m (a circle centering AP with the diameter of 10m)
Maximum data rate 11Mbps
3.6 Data Storage
Long trend: 96 hours, resolution 1min, 5 min or 10 min.

Trend data
Short trend: 1 hour, resolution 1 s or 5 s.
70 alarm events and associated waveforms (with user

Alarm events
selectable waveform length 8s, 16 or 32).
ARR events 80 ARR events and associated waveforms with 8s wavelength.
800 NIBP groups, including systolic pressures, mean pressures,

NIBP measurements
diastolic pressures and measurement time.
3-5
3.7 Signal Output Specifications
Meets the requirements of EC60601-1 for short-circuit

Standards
protection and leakage current
Output impedance 50O
ECG analog output
0.05 to 100Hz(12-lead: 0.05 to

Bandwidth Diagnostic mode:
150Hz)
(-3dB; reference Monitor mode:
0.5 to 40Hz
frequency: 10Hz) Surgery mode:
1 to 20Hz
Signal delay = 25ms
Maximum propagation delay 25ms (In DIAGNOSTIC mode, NOTCH is OFF)
Sensitivity 1V/mV±5%
PACE rejection/enhancement No pace rejection or enhancement
IBP analog output
Bandwidth 0 to 12.5 Hz (-3dB, reference frequency: 1Hz)
Maximum propagation Delay 55ms (the filter function is disabled)
Sensitivity 1 V/100mmHg±5%
Nurse call output

Driver Relay
Electrical specifications =60W, =2A, =36VDC, =25VAC
Isolation voltage > 1500 VAC
Signal type Normally open or normally closed, selectable
Defibrillator synchronization pulse
Maximum time delay 35ms (R-wave peak to leading edge of the pulse)
Amplitude 3.5 V (min) at 3 mA sourcing; 0.8 V (max) at 1 mA sinking
Pulse width 100 ms ±10%
Rising and falling time < 3ms
VGA
Signal RGB: 0.7 Vp-p/75O;

Horizontal/vertical synchronization: TTL level
3-6
3.8 ECG Specifications
3-lead (1 channel): I, II, III

Lead type 5-lead (2 channels): I, II, III, aVR, aVL, aVF and V
12-lead (8 channels): I, II, III, avR, avL, avF, V1-V6
Lead naming style AHA, EURO
1.25mm/mV (×0.125), 2.5mm/mV (×0.25), 5mm/mV (×0.5),

Sensitivity selection
10mm/mV (×1), 20mm/mV (×2) and auto
Sweep speed 12.5mm/s, 25mm/s, 50mm/s
Diagnostic mode: 0.05 to 100Hz (12-lead: 0.05 to 150Hz)

Bandwidth (–3dB) Monitor mode: 0.5 to 40Hz
Surgery mode: 1 to 20Hz
Diagnostic mode: =90 dB (12-lead: >95 dB)

Monitor mode: =105 dB
Common mode rejection
Surgery mode: =105 dB
(The notch filter is turned off.)
Differential input
= 5MO
impedance
Input signal range ±8mV (peak-to-peak value)
DC offset voltage ±300mV (12-lead: ±500mV)
Patient leakage current < 10uA
Recovery time after

< 3s
defibrillation
Calibration signal 1mV (peak-to-peak value), precision: ±5%
HR
Neonate: 15 to 350 BPM

Measurement range Pediatric: 15 to 350 BPM
Adult: 15 to 300 BPM
Resolution 1 BPM
Precision ±1BPM or ±1%, whichever is greater.
Sensitivity 200µV (lead II)
3-7
Meets the requirement of ANSI/AAMI EC13-2002: Section

Response time to heart rate 4.1.2.1 f).
changes Less than 11 sec for a step increase from 80 to 120 BPM
Less than 11 sec for a step decrease from 80 to 40 BPM
When tested in accordance with ANSI/AAMI EC13-2002 Section

4.1.2.1 g, the response time is as follows.
Figure 4ah –range: 15.7 to 19.2s, average: 17.4s

Response time of 4a –range: 5.7 to 8.5s, average: 7.5s
tachycardia alarm 4ad –range: 3.6 to 5.1s, average: 4.2s
Figure 4bh –range: 11.5 to 14.7s, average: 12.9s
4b –range: 4 to 14s, average: 7.2s
4bd –range: 6.6 to 14.5s, average: 10.5s
Pace pulse
Pace pulses meeting the following conditions are marked by the

PACE indicator.
Pulse indicator Amplitude: ±4 to ±700mV
Width: 0.1ms to 2ms
Rise time: 10us to 100µs
When tested in accordance with the ANSI/AAMI EC13-2002:

Sections 4.1.4.1 and 4.1.4.3, the heart rate meter rejects all pulses
meeting the following conditions.
Pulse rejection Amplitude: ±2 to ±700mV

Width: 0.1ms to 2ms
Rise time: 10us to 100µs
Min. input slew rate: 50V/s RTI
ST segment measurement
Measurement range –2.0 to +2.0 mV
–0.8 to +0.8mV: ±0.02mV or ±10%, whichever is

Precision greater.
Beyond this range: Undefined.
Update period 10s
Arrhythmia analysis
ASYSTOLE, VFIB/VTAC, PVC, COUPLET, VT>2,

Type BIGEMINY, TRIGEMINY, R ON T, MISSED BEATS, TACHY,
BRADY, PNC and PNP
3-8
3.9 RESP Specifications
Measurement technique Thoracic impedance
Lead Optional: lead I and lead II; default lead II
Differential input
> 2.5MO
impedance
Respiration impedance test

0.3 to 3O
range
Excitation current < 300µA
Baseline impedance range 200 to 2500O (using an ECG cable with 1kO resistance)
Bandwidth 0.2 to 2Hz (-3 dB)
Sweep speed 6.25 mm/s, 12.5 mm/s, 25 mm/s
RR
Adult: 0 to 120 BrPM

Measurement range
Pediatric/neonate: 0 to 150 BrPM
Resolution 1 BrPM
7 to 150 BrPM: ±2 BrPM or ±2%, whichever is greater.

Precision
0 to 6 BrPM: Undefined.
Apnea alarm delay 10 to 40s
3-9
3.10 SpO2 Specifications
Mindray SpO2 Module
SpO2
Measurement range 0 to 100%
Resolution 1%
70 to 100%: ±2 % (adult/pediatric, non-motion conditions)

70 to 100%: ±3 % (neonate, non-motion conditions)
Precision
70 to 100%: ±3 % (in motion conditions)
0% to 69%: Undefined.
Refreshing rate 1s
PR
Measurement range 20 to 254bpm
Resolution 1bpm
±3 bpm (non-motion conditions)

Precision
±5 bpm (in motion conditions)
Refreshing rate 1s
Masimo SpO2 Specifications
SpO2
Measurement range 1 to 100%
Resolution 1%
70 to 100%: ±2% (adult/pediatric, non-motion conditions)

70 to 100%: ±3% (neonate, non-motion conditions)
Precision
70 to 100%: ±3% (in motion conditions)
0% to 69%: Undefined.
Refreshing rate 1s
3-10
PR
Measurement range 25 to 240bpm
Resolution 1bpm
±3bpm (non-motion conditions)

Precision
±5bpm (in motion conditions)
Refreshing rate 1s
Nellcor SpO2 Specifications
Sensor Range Precision*
MAX-A, MAX-AL, MAX-N, 70 to 100% ±2%

MAX-P, MAX-I and MAX-FAST 0% to 69% Undefined
OxiCliq A, OxiCliq N, OxiCliq P, 70 to 100% ±2.5%

SpO2 measurement range
OxiCliq I 0% to 69% Undefined
and precision
D-YS, DS-100A, OXI-A/N and 70 to 100% ±3%
OXI-P/I 0% to 69% Undefined
70 to 100% ±3.5%
MAX-R, D-YSE and D-YSPD
0% to 69% Undefined
PR measurement range and 20 to 250bpm: ±3bpm

precision 251 to 300bpm: Undefined
Refreshing rate 1s
*: When sensors are used on neonatal subjects as recommended, the specified precision range is
increased by ±1%, to account for the theoretical effect on oximeter measurements of fetal
hemoglobin in neonatal blood.
3-11
3.11 IBP Specifications
Measurement technique Auto oscillation
Displayed parameters Systolic pressure, diastolic pressure and mean pressure
Mode of operation Manual, auto and continuous
Measurement interval in
1/2/3/4/5/10/15/30/60/90/120/180/240/480 minutes
auto mode
Measurement time in
5 minutes
continuous mode
mmHg Adult Pediatric Neonate
Systolic
40 to 270 40 to 200 40 to 135
Measurement range in pressure
normal mode Diastolic
10 to 210 10 to 150 10 to 100
pressure
Mean pressure 20 to 230 20 to 165 20 to 110
Maximum average error: ±5mmHg

Measurement precision
Maximum standard deviation: 8mmHg
Resolution 1mmHg
Adult: 297±3 mmHg

Over-pressure protection Pediatric: 240±3 mmHg
Neonate: 147±3 mmHg
3-12
3.12 TEMP Specifications
Number of channels 2
Displayed parameters T1, T2 and TD
Measurement range 0 to 50°C (32 to 122°F)

Resolution 0.1°C
0.1°C (excluding the sensor)

Precision
±0.2°C (including the YSI 400 series sensor)
Update period 1s
Body surface: < 100s

Minimum time for
Body cavity: < 80s
accurate measurement
(YSI 400 series sensor)
3.13 IBP Specifications
Number of channels 2
Pressure labels ART, PA, CVP, RAP, LAP, ICP, P1 and P2
ART 0 to 300 mmHg
PA –6 to 120 mmHg
Measurement range
CVP/RAP/LAP/ICP –10 to 40 mmHg
P1/P2 –50 to 300 mmHg
Resolution 1 mmHg
Precision ±2% or ±1mmHg, whichever is greater
Update period 1s
Pressure transducer
Sensitivity 5 uV/V/mmHg
Impedance range 300 to 3000O
3-13
3.14 CO Specifications
Measurement technique Thermal dilution
Calculated parameter CO, hemodynamics
CO 0.1 to 20l/min
Measurement range TB 23 to 43°C
TI 0 to 27°C
CO: 0.1 l /min

Resolution
TB, TI: 0.1°C
CO: ±5% or ± 0.1 l /min

Precision
TB, TI: 0.1°C
TB
Alarm range 23 to 43°C
:
3-14
3.15 CO2 Specifications

Measurement technique Infrared absorption technique
Measurement mode Sidestream, microstream or mainstream (optional)
Displayed parameter EtCO2, FiCO2, Respiration Rate
CO2 function Meet the requirements of EN864 and ISO9918.
Mindray CO2 Specifications
CO2 measurement range 0 to 99mmHg
0 to 40 mmHg: ±2mmHg
Precision* 41 to 76 mmHg: ±5%
77 to 99 mmHg: ±10%
Deflation rate 100, 150ml/min
Precision of deflation rate 15%
< 1min.
Start-up time of CO2
The module enters the warming up status after the startup. Ten
module
minutes later, it enters the ready-to-measure status.
AwRR measurement range 0 to 120 BrPM
0 to 70 BrPM: ±2 BrPM
Precision
> 70 BrPM: ±5 BrPM
Response time < 240 ms (10 to 90%)
< 2s (Length of sampling tube: 7 feet; inner diameter: 0.055

Delay time
inches; sampling flow: 150ml/min)
Apnea alarm delay AwRR: 10 to 40 s
* Conditions for measurements in typical precision:

The measurement is started after the preheating mode of the module;
Ambient pressure: 750mmHg to 760mmHg; room temperature: 22℃ to 28℃;
The gas under test is dry, and the balance gas is N2;
The deflation rate is 150ml/min, the respiration rate is no greater than 30BrPM, with a
fluctuation less than ±3BrPM, and the inhale interval/exhale interval is 1:2;
In other conditions, the measurement precision should meet the requirements of EN864 or
ISO9918: ±4mmHg (0 to 40mmHg) or ±12% of the reading (41 to 99mmHg)
3-15
Oridion CO2 Specifications
Precision*
39 to 99 mmHg: ±5% + 0.08%× (reading - 38mmHg)
Waveform: 0.1mmHg
Resolution
Value: 1mmHg
Flow rate 50 −+7.5

15 ml/min
Initialization time 30s (typical)
Response time 2.9s (typical)
Delay time 2.7s (typical)
0 to 70BrPM: ±1BrPM
AwRR measurement
precision
Apnea alarm delay AwRR: 10 to 40s
* Precision applies for breath rates of up to 80 bpm. For breath rates above 80 bpm, accuracy
complies with EN 864/ISO 9918 (4 mmHg or ±12% of reading whichever is greater) for EtCO2
values exceeding 18 mmHg. To achieve the specified accuracies for breath rates above 60
breaths/minute, the Microstream® FilterLine H Set for Infant/Neonatal (p/n 006324) must be
used.
The accuracy specification is maintained to within 4% of the values indicated in the above table
in the presence of interfering gases according to EN864 Section Eleven, Part 101.
3-16
Welch Allyn CO2 Specifications
Precision* 41 to 76 mmHg: ±5%
77 to 99 mmHg: ±10%
Resolution 1mmHg
Refreshing rate 1s
< 80s (ambient temperature: 25℃; preheating power of

Start-up time
transducer: 5W)
Response time 100ms (10% to 90 %)
Calibration Daily calibration is unnecessary
There is a difference (< 1%) from the precison criteria after a

Calibration stability
12-month continuous service time
Alarm range 0 to 99 mmHg
AwRR alarm range 0 to 150 BrPM
Apnea alarm delay AwRR: 10 to 40 s
* Precision specification is based upon the following standard airway conditions: sensor 42℃;
airway adapter temperature 33℃; water vapor pressure 38 mmHg; standard gas mixture equals
CO2 in balance air; fully hydrated at 33℃; atmospheric pressure 760 mmHg; airway flow rate
60 cc/min.
3-17
3.16 AG Specifications
Measurement technique Infrared absorption
Measurement mode Side stream
AG functions Meets requirements of ISO9918, ISO11196, EN12598 and ISO7767
45 seconds (warming-up status)

Warm-up time
10 minutes (ready-to-measure status)
Sampling flow Adult/Pediatric 120, 150, 200 ml/minute (user-selectable)

(sidestream) Neonatal 70, 90, 120 ml/minute (user-selectable)
Gas type CO2, N2O, O2 (optional), Des, Iso, Enf, Sev, Hal
CO2: 0 to 30%
N2O: 0 to 105%
Des: 0 to 30%
Measurement range Sev: 0 to 30%
Enf, Iso, Hal: 0 to 30%
O2: 0 to 105%
AwRR: 2 to 100 BrPM
CO2: 1 mmHg
Resolution
AwRR: 1 BrPM
Precision Gas Range (%REL) Precision (%ABS)
0 to 1 ±0.1
1 to 5 ±0.2
CO2 5 to 7 ±0.3
7 to 10 ±0.5
> 10 Not specified
0 to 20 ±2
N2O
20 to 100 ±3
Des 0 to 1 ±0.15
1to 5 ±0.2
5 to 10 ±0.4
10 to 15 ±0.6
3-18
15 to 18 ±1
>18 Not specified
0 to 1 ±0.15
1 to 5 ±0.2
Sev
5 to 8 ±0.4
>8 Not specified
0 to 1 ±0.15
Enf, Iso, Hal 1 to 5 ±0.2
>5 Not specified
0 to 25 ±1
O2 (Optional) 25 to 80 ±2
80 to 100 ±3
2 to 60 BrPM ±1 BrPM
AwRR
> 60 BrPM Not specified
CO2: 0 to 10 % (0 - 76 mmHg)
Alarm range
AwRR: 2 to 100 BrPM
Apnea alarm delay AwRR： 20 - 40 s
Refreshing rate 1s
Calibration Yearly calibration requested.

Calibration stability After module being used for 12 consective months, the error is < 1%
Rise time (10 % to 90 %) CO2 250 ms (fall time 200 ms)
Sampling flow N2O 250 ms
120ml/min, using the
DRYLINE™ water trap O2 600ms
and neonatal HAL, ISO, SEV, DES 300 ms
DRYLINE™ sampling
ENF 350 ms
line (2.5m)
Rise time (10 % to 90 %) CO2 250 ms (fall time 200 ms)
Sampling flow N2O 250 ms

200ml/min, using the
O2 500ms
DRYLINE™ water trap
and adult DRYLINE™ HAL, ISO, SEV, DES 300 ms
sampling line (2.5m) ENF 350 ms
Delay time < 4s
3-19
FOR YOUR NOTES
3-20
Disassembling/Assembling & Troubleshooting
Chapter 4 Disassembling/Assembling
& Troubleshooting
4.1 PM-9000 Super Disassembling/Assembling

4.1.1 Exploded View of PM-9000 Super
Figure 4-1 Exploded view of PM-9000 Super
NO Material code Part & Specification Quantity

1 9201-30-11414 Front cover assembly 1
2 9300-30-13912 Back plate assembly 1
3 M04-000305--- Cross-head self-tapping screw 3*12 5
4 M02-000802--- Flat washer GB97.13 4
5 9201-30-35944 Support assembly (Lithium battery) 1
6 9201-20-35971- Battery door 1
7 M04-003105--- Cross-head self-tapping screw M3*8 3
8 9201-30-35948 6pin parameter socket 1
9 9201-30-35992 Back cover assembly (microstream CO2) 1
10 TR6C-30-19654 TR6D-C recorder 1
11 M04-004012--- Gasketed cross-head screw M3*6 2
14 M04-051140--- Screw assembly M3*8 2
4-1
4.1.2 PM-9000 Super Display (TFT Display) Assembly
Figure 4-2 PM-9000 Super display (TFT display) assembly

NO Standard Name & Specification Quantity
1 ９３００－２０－１３９１１　 10.4’TFT display fixture ２　
2 ００００－１０－１１０２１　 LCD TFT 10.4’display ８００＊６００　３．３Ｖ１　
3 Ｍ０４－０５１１３７－－－　 Cross-head screw M 2*4 ４　
4 ９３００－２０－１３９１０　 10.4’TFT display fixture １　
5 Ｍ０４－００４０１２－－－　 Cross-head screw M3*6 ４　
6 ９３００－２０－１３９０１　 Insulating washer １　
7 ００１０－１０－１２０９６　ＤＣ／ＡＣ　１２ＶＤＣ　５００Ｖｒｍｓ　６ｍＡ１　
8 Ｍ０４－００２４０５－－－　 Cross-head screw M2*6 ２　
4-2
4.1.3 PM-9000 Super Support Assembly (Lithium Battery) (9201-30-35944)
Figure 4-3 PM-9000 Super support assembly

NO Material Code Part & Specification Quantity
2 9200-20-10689 Recorder regulating panel 1
3 9200-20-10485 Printer mounting plate 1
4 M04-005005--- Cross-head sunk screw M3*6 14
5 9201-20-35965 Support 1
6 M04-002505--- Cross-head screw M3*6 10
7 9201-30-35954 CF wireless network adapter assembly 1
8 9210-30-30150 9210 main control board 1
9 9201-30-35922 Battery compartment assembly (Lithium 1
battery)
10 0010-10-12329 Lithium battery 2
11 9200-20-10516 Insulating plate of ECG board 1
12 812A-30-08557 812A ECG board 1
13 M04-060009--- Stud M3*14 1
14 9200-20-10677 Insulating plate of mounting plate 3 1
15 9200-20-10676 SPO2/IBP mounting plate 1
17 M03A-30-90293 IBP/CO module 1
18 630D-30-09121 630D blood pressure pump 1
19 0010-10-12274 MASIMO SpO2 module 1
4-3
20 9201-20-36012 Power PCB insulating plate 1

21 9201-30-35901 Lithium battery power PCB 1
22 9210-30-30163 Socket assembly 1
23 9201-30-35908 Microstream CO2 adapter board 1
24 9201-30-35955 Microstream CO2 module 1
25 9201-20-35928 Mounting plate of microstream CO2 1
module
4.1.4 Front Cover Assembly
Figure 4-4 Front cover assembly

NO Material Code Part & Specification
15 9000-20-07356 Power Button 2
14 9000-20-07355 Button panel 2
13 9200-30-10470 Encoder plate
12 9000-20-07347 Front Cover 2
11 9200-20-10464 10.4 TFT panel
10 8000-20-10205 Rotary knob
9 9000-20-07458 Foot plate 3
8 M04-000102--- Flat washer
7 900E-20-04890 Alarm indicator cover
6 M04-051003--- Cross-head self-tapping screw PT2.0*6
5 0010-30-42658 Button backer
4 M04-003105--- Cross-head self-tapping screw PT 3*8
3 900E-20-04892 Connector
2 900E-20-04894 Dust washer1
1 900E-20-04895 Dust washer2
4-4
4.1.5 Back Cover Assembly
Figure 4-5 Back cover assembly (microstream CO2) (9201-30-35992)

NO Material Code Part & Specification Remark
1 M04-003105--- Cross-head self-tapping screw 3*8
2 9200-20-10620 Speaker press plate
3 9200-21-10633 Speaker
4 9200-20-10622 Hook mounting plate
5 9201-21-35974 Back cover (microstream CO2 module)
6 9201-20-35970 Handle
7 9201-20-35969 Gland
8 M04-000802--- Flat washer GB9713
10 9201-30-35923 Mounting assembly of microstream CO2
connector
11 6200-20-11614 CO2 nozzle
12 9200-20-10511 Foot plate 1
13 M04-000501--- Stainless steel nut GB6170MS
14 9201-30-35978 Fan assembly
4-5
4.1.6 Microstream CO2 Assembly
Figure 4-6 Microstream CO2 assembly

NO Material Code Part & Specification
1 9201-30-35959 Microstream CO2 connector
3 9201-20-36010 Baffle of torsional spring
4 9201-20-35961 Retaining torsional spring of microstream CO2
connector
5 9201-20-35915 Mounting plate of CO2 connector
6 9201-20-35914 Baffle of CO2 connector
4.2 Troubleshooting
4-6
4.2.1 Black Screen, Startup Failure
Figure 4-7 Location flow of faults causing black screen
4-7
4.2.2 White Screen & Other Abnormal Screen

In case of faults causing white screen or other abnormal screens,
■　 Check whether the LCD connection wires are in good contact;
■　 Replace the LCD connection wires, or replace the LCD if necessary;
■　 Replace the main control board if the fault still exists.
4.2.3 Encoder Faults

1. If all other functions (indicator, alarm, buttons) of the button panel are normal,
proceed to step 2; otherwise, replace the button panel;
2. Check whether short-circuit or abnormal open-circuit occurs in the encoder pad;
3. Replace the encoder.
4.2.4 No Audio Alarm

1. Check whether the audio alarm function is disabled in the software settings;
2. Replace the speaker;
3. Replace the button panel.
4.2.5 Printing Failure

1. Check whether there is any alarm about the recorder. If any, eliminate it;
2. Check whether the recorder indictor is on;
3. If not, check the connection wire for inputting signals to the recorder;
4. Check whether the recorder module is enabled in the maintenance menu;
5. Check the power cord of the recorder (including the recorder power PCB);
6. Replace the recorder module.
4.2.6 Abnormal Paper Drive

1. Check whether there are blocks on the paper roller of the recorder;
2. Check whether there are blocks in the gear cluster of thermal assembly of the
recorder;
3. Check whether the voltage input of the recorder is larger than 17.6V.
4-8
Test and Material List
Chapter 5 Test and Material List

5.1 Test Procedure
5.1.1 Connection and Checking
Connect the simulators, power supply and test fixture properly to the PM-9000 Super
patient monitor, and power it on. Then, the patient monitor displays the start-up screen on
the TFT screen and enters the system screen.
5.1.2 Functions of Buttons

Press every button on the button panel to check their functions as specified in PM-9000
Super Operation Manual. Rotate the control knob to check its functions.
5.1.3 ECG/RESP
The TFT screen displays the standard ECG waveform, and the error between the heart
rate and the set value of the simulator is no more than ±1, namely 60±1; the RESP
waveform is smooth, and the respiration rate is 20±1.
1. Select all leads in order, including Cal, select all the four gains and AUTO, ensure
the waveforms are displayed properly, and check whether the 50Hz/60Hz
interference can be filtered.
2. Check, in all the above-mentioned cases, the consistency between the
heartbeats, the flashes of the red heart-like indicator, and the R-wave.
3. The gain has no impact on the message “ECG signal over weak” in the HR
calculation.
4. Verify the range and precision: Suppose that the amplitude of the GCG signal of
the simulator is 1mV, the heart rates are respectively 30, 60, 120, 200, 240 and
300. Check leads I, II and III. The results should meet 29-31, 59-61, 119-121,
198-202, 238-242, and 297-303.
5. PACE pulse test: Set the simulator to PACE. You should be able to view the pace.
Change PACE amplitude to ±8 – 700mv, and pulse width to 0.1ms – 2ms. The
PACE should be legible, and LEAD OFF is displayed properly.
6. RESP measurement: Set the baseline impedance to 1K, the respiration
impedance to 0.5O and 3O, and the respiration rate to 30 and 120. The
respiration rate should be 29 – 31, 118 –122.
7. PVC test: Set the simu lator to the PVC mode, and set the occurrence times. The
relevant PVCS should be obtained.
8. Set the simulator as follows: RR: 40, baseline impedance: 2KO, RESP waveform:
3:1. Open the apnea alarm, set the respiration resistance to 0O, and set various
alarm time. Alarms should be given.
5.1.4 Temperature
1. YSI probe
Select YSI probe from the manufacturer menu, select YSI temperature probe as
the test fixture, set the analog resistance to 1.471K, 1.355K and 1.249K. Then
the TEMP parameter should be 35±0.1℃ , 37±0.1℃ and 39±0.1℃ .
5-1
2. CY-F1 probe
Select CY-F1 probe from the manufacturer menu, select CY-F1 temperature
probe as the test fixture, set the analog resistance to 6.534K, 6.018K and
5.548K. Then the TEMP parameter should be 35±0.1℃ , 37±0.1℃ and
39±0.1℃ .
5.1.5 NIBP
Connect the NIBP simulator, adult cuff and accessories, and then connect the module
CUFF and clockwise screw it tightly.
1. After the simulator self-test, press <ENT> to enter the ADULT analog blood
pressure mode. Set the blood pressure to the 255/195/215 mmHg level, SHIFT
to +15, and the HR to 80BPM. Set PM-9000 Super to the adult mode. Press
<START>. Then the results will be obtained in about 30s. The measured results
should be respectively 270±8mmHg, 210±8mmHg and 230±8mmHg.
2. Press <ESC> and <?> on the simulator to enter the NEONATE mode. Set the
blood pressure to the 120/80/90 mmHg level, HR to 120bmp, and PM-9000
Super to the pediatric mode. Press <START>. Then the results will be obtained
in about 30s. The measured results should be respectively 120±8mmHg,
80±8mmHg and 90±8mmHg.
3. Press <ESC> and <?> on the simulator to enter the NEONATE mode. Set the
blood pressure to the 60/30/40 mmHg level, SHIFT to -20, HR to 120bmp, and
PM-9000 Super to the neonate mode. Change the simulator accessory to the
neonatal cuff. Press <START>. Then the results will be obtained in about 30s.
The measured results should be respectively 40±8mmHg, 10±8mmHg and
20±8mmHg.
5.1.6 SpO2
Select PLETH as the HR source of PM-9000 Super, and put the finger into the SpO2
sensor. The screen should display the PR and SpO2 values normally. The normal SpO2
value is above 97%.
5.1.7 IBP
1. Test fixture
Physiological signal simulator
2. Test procedure
　 ① IBP1 test:
Set the BP sensitivity of the ECG simulator to 5uv/v/mmHg, BP to 0mmHG, and the
IBP channel 1 to ART. Enter the IBP PRESSURE ZERO menu of the PM-9000
Super, zero Channel 1, and then return to the main screen. Set the BP of the
simulator to 200mmHg. Enter the IBP PRESSURE CALIBRATE menu of the
PM-9000 Super, conduct calibration, and then exit the IBP PRESSURE CALIBRATE
menu.
Set the BP value of the simulator respectively to 40mmHg, 100mmHg and
200mmHg. Then the screen of the PM-9000 Super should display 40±1mmHg,
100±2mmHg and 200±4mmHg.
Set the simulator output to ART wave. Then the screen of the PM-9000 Super
5-2
should display relevant waveform properly.

Unplug the IBP probe. Then the screen should prompt “IBP: Transducer 1 OFF!”
and “IBP: Transducer 2 OFF!”
Plug the OHMEDA cable to the IBP1 channel. Then the prompting message “IBP:
Transducer 1 OFF!”disappears.
　　② IBP2 test:
Plug the IBP cable to the IBP2 channel, and repeat the procedure in Section ① .
5.1.8 CO
1. Test fixture
Physiological signal simulator
　 2. Test procedure
Injectate and blood temperature test: Assemble the TB and TI test fixture, output
three TB temperature values: 36℃ , 37℃ and 38℃ . Then TB should be respectively
36.0±0.1℃ , 37.0±0.1℃ and 38.0±0.1℃ . Set the injectate switch to ON, output two
TI temperature values: 0℃ and 2℃. Then the screen should display 0±0.1℃ and
2.0±0.1℃ .
CO measurement: Set the CO.CONST and TI to the default values: 0.542 and 0℃ ,
set the injectate switch to OFF, and then press START. Then the simulator will
output 0℃ , 2.5L/M and 0℃ , 5L/M within 2s. The CO values should be 2.5±0.25L/M
and 5±0.5L/M.
5.1.9 CO2
1. Test fixture
CO2 steel bottle (containing 10% CO2)
2. Test procedure
① Mainstream CO2 measurement: Set the calculation compensation of PM-9000
Super to COMMON.
Plug the mainstream transducer to the CO2 socket, connect the windpipe connector
with the CO2 steel bottle, and open/close the valve of the CO2 steel bottle based on
the interval of 3s. The CO2 value should be the calibration gas pressure value:
76±5%mmHg. When the valve is opened permanently, the patient monitor prompts
“APNEA ALARM”.
Unplug the transducer. The patient monitor prompts “CO2 transducer OFF”on
the main screen. Plug the transducer again. The patient monitor prompts “CO2
transducer pre-heated”.
② Sidestream CO2 measurement: Set the calculation compensation of PM-9000
Super to COMMON.
Plug the water trap to the water trap socket, connect the sampling tube with the CO2
steel bottle, and open//close the valve of the CO2 steel bottle based on the interval of
3s. The CO2 value should be the calibration gas pressure value: 76±5%mmHg. When
the valve is opened permanently, the patient monitor prompts “APNEA ALARM”.
Unplug the water trap. The patient monitor prompts “CO2 water trap OFF”. Plug the
water trap again. The prompting message disappears.
③ When the measured value exceeds the high limit of CO2, the patient monitor
prompts “CO2 too high”on the main screen. When the measured value is lower
5-3
than the low limit, the patient monitor prompts “CO2 too low”.
5.1.10 Recorder
1. Print the ECG waveform. The recorder should print it normally and clearly. Set
the recorder to the fault of lack of paper and abnormal clip. There should be relevant
prompting messages on the main screen. When the fault is cleared, the patient
monitor should become normal.
2. Print the alarm messages of all parameters. Set the alarm print switch to ON for
all parameters, and set different alarm limits. Then the recorder should print the
alarm message in case of an alarm.
5.1.11 Power Supply

When the patient monitor is supplied with the external AC power, the power indicator
becomes ON. When it is disconnected from the external AC power, the power
indicator becomes OFF. After the patient monitor is started without assembling the
batteries, “x”is displayed in the battery indication frame on the main screen. After the
batteries are assembled, the battery electricity is displayed in the battery indication
frame on the main screen. The patient monitor can work normally with or without
batteries. It, however, should give an alarm when the batteries are exhausted.
5.1.12 Clock
Verify the correctness of the clock in the system test, and then set the clock to the current time.
5.1.13 System Test

Load all parameters, and conduct operations respectively on the loaded parameters.
During the synchronization, no exceptions (for example, mutual interference) occur.
Set all parameter setups in menus to the default values which are those at the time of
software loading, and conduct operations on the menus, for example, managing the
patient information, recalling data, and so on. All the operations should be done
normally, and the corresponding functions should be correct and meet the product
requirements.
5-4
5.2 NIBP Calibration
Figure 5-1 NIBP Calibration

Calibration method:
Based on the precision of 50mmHg (6.7kPa), increase the pressure step by step. The
maximum error at any pressure point within the NIBP measurement range of the patient
monitor should be no more than ±3mmHg (±0.4kPa). Decrease the pressure step by step.
The maximum error at any pressure point within the NIBP measurement range of the patient
monitor should be no more than ±3mmHg (±0.4kPa).
5.3 IBP CALIBRATE
5.3.1 IBP Transducer Zero
n Press the ZERO button on the IBP module to call up IBP PRESSURE ZERO menu as
shown below:
Figure 5-2 IBP PRESSURE ZERO
5-5
Zero Calibration of Transducer

Select CH1, the system will zero IBP1. Select CH2, the system will zero IBP2.
Cautions:( Use the PM-6000 IBP module as a example)
n Turn off patient stopcock before you start the zero procedure.
n The transducer must be vented to atmospheric pressure before the zero procedure.
n The transducer should be placed at the same height level with the heart, approximately
mid-axially line.
n Zero procedure should be performed before starting the monitoring and at least once a
day after each disconnect-and-connect of the cable.
Figure 5-3 IBP Zero
5.3.2 IBP Calibration
n Press CAL button on the IBP module to call up the IBP PRESSURE CALIBRATE menu as
shown below:
5-6
Figure 5-4 IBP Calibration Menu
Calibrate the transducer:
Turn the knob to select the item CH1 CAL VALUE, press and turn the knob to select the
pressure value to be calibrated for channel 1. Then turn the knob to select the item
CALIBRATE to start calibrating channel 1.
Turn the knob to select the item CH2 CAL VALUE, press and turn the knob to select the
pressure value to be calibrated for channel 2. Then turn the knob to select the item
CALIBRATE to start calibrating channel 2.
n The pressure calibration of PM-9000 Super:
Figure 5-5 IBP Calibration
You will need the following pieces of equipment:

• Standard sphygmomanometer
• 3-way stopcock
• Tubing approximately 25 cm long
5-7
The Calibration Procedure:
1. Close the stopcock that was open to atmospheric pressure for the zero calibration.
2. Attach the tubing to the sphygmomanometer.
3. Ensure that connection that would lead to patient is off.
4. Connect the 3-way connector to the 3-way stopcock that is not connected to the patient
catheter.
5. Open the port of the 3-way stopcock to the sphygmomanometer. .
6. Select the channel to be calibrated in the menu and select the pressure value to which the
IBP is to be adjusted.
7. Inflate to make the mercury bar rise to the setup pressure value.
8. Adjust repeatedly until the value in the menu is equal to the pressure value shown by the
mercury calibration.
9. Press the Start button, the device will begin calibrating.
10. Wait for the calibrated result. You should take corresponding measures based on the
prompt information.
11. After calibration, disassemble the blood pressure tubing and the attached 3-way valve.
Calibration completion message:
“SUCCESSFUL CALIBRATE”
5.4 CO2 CHECK

Check procedure for sidestream module only
Via the PM-9000 Super’
s system and maintain menus you are prompted for a password for
entering the factory key. After entering the password “332888”you get access to the pump rate
settings and to check the accuracy of the CO2 measurement. Using the below test set up to
verify the accuracy of the CO2 module.
Figure 5-6 Sidestream test set up
5-8
Note Neither the mainstream nor the sidestream module can be calibrated. Only the
overall performance and accuracy is checked. If the Co2 module fails the tests it should be
replaced.
Figure 5-7 Factory Maintain Menu Figure 5-8 CO2 check menu
5.5 AG CALIBRATE
5.5.1 AG Check
1、Using T-piece to connect the watertrap and Agent steel bottle well. One of the T-piece ports
must be vented to atmospheric pressure.
2、Select ‘MEASURE’from work mode item in “AG SETUP”menu, then set pump rate ‘
low’
and wait for 10 minutes after the warm up information disappears.
3、Enter ‘
CALIBRATE’menu, then open AG bottle and press the ‘
VERIFY ACCURACY’item.
Figure 5-9 AG Check Menu

4、Observe the display value after 1 minute. The agent concentration accurate should be less than
±5%.
5、Choose other pump rate ‘ high’，and repeat the previous procedures.
middle’or ‘
(pump rate definition: three pump rate under adult mode: 100/150/200ml/min; neonate:
70/90/110 ml/min）
6、If the accurate over range, please press ‘
START CAL’
.
5-9
5.5.2 AG CALIBRATE
（Agent>1.5%, CO2>1.5%, N2O>40%, O2>40% ）

1、Press ‘
START CAL’
, then input password ‘
MINDRAY’entering ‘
CALIBRATE’menu.
Note: Make sure the AG in ‘
Measure’mode not ‘
Standby’mode before you do calibrate.
Figure 5-10
Figure 5-11
2、Input each gas concentration value according to the label on the AG bottle label.
Note: If your monitor do not have O2 module, input ‘
0.0’in O2 item.
3、Open AG cover, wait for the display value stabilization.
4、If the display value does not accord with the input value, please press ‘
CALIBRATE’item
and exit.
AG concentration must fit the following requirements:
Agent>1.5%, CO2>1.5%, N2O>40%, O2>40%
5-10
5.6 PM-9000 Super Material List

NO Material Code` Name & Specification Quantity
2 9200-20-10689 Recorder regulating panel 1
3 9200-20-10485 Printer mounting plate 1
4 M04-005005--- Cross-head sunk screw M3*6 14
5 9201-20-35965 Support 1
6 M04-002505--- Cross-head screw M3*6 10
7 9201-30-35954 CF wireless network adapter assembly 1
8 9210-30-30150 9210 main control board 1
9 9201-30-35922 Battery compartment assembly (Lithium 1
battery)
10 0010-10-12329 Lithium battery 2
11 9200-20-10516 Insulating plate of ECG board 1
12 812A-30-08557 812A ECG board 1
13 M04-060009--- Stud M3*14 1
15 9200-20-10676 SPO2/IBP mounting plate 1
17 M03A-30-90293 IBP/CO module 1
18 630D-30-09121 630D blood pressure pump 1
19 0010-10-12274 MASIMO SpO2 module 1
20 9201-20-36012 Power PCB insulating plate 1
21 9201-30-35901 Lithium battery power PCB 1
22 9210-30-30163 Pinboard assembly 1
23 9201-30-35908 Microstream CO2 adapter board 1
24 9201-30-35955 Microstream CO2 module 1
25 9201-20-35928 Mounting plate of microstream CO2 1
module
5-11
FOR YOUR NOTES
5-12
Maintenance and Cleaning
Chapter 6 Maintenance and Cleaning

6.1 Maintenance
6.1.1Checking Before Using
■　 Check the patient monitor for mechanical damages;
■　 Check all exposed conductors, connectors and accessories;
■　 Check all functions that are possibly enabled for the monitored patient, and
ensure the device is in good working status.
In case of any damage, stop using this patient monitor, and contact biomedical
engineers of the hospital or Mindray maintenance engineers.
6.1.2 Regular Checking

An all-around check, including the safety check, should be done by qualified personnel
every 6-12 months or after maintenance each time.
All checks in which the patient monitor should be disassembled should be done by
qualified maintenance personnel. The safety and maintenance checks can be done by
Mindray engineers. The local office of Mindray at your region will be pleased to provide
you with the information about the maintenance contract.
6.2 Cleaning
Do switch off the patient monitor and disconnect the AC power supply before
cleaning it or the probes.
The PM-9000 Super patient monitor should be dust free. To clean the surface of its
enclosure and screen, use the cleaning agent that is not corrosive, for example, soap
and water.
1. Do not use strong solvent, such as acetone;
2. Most cleaning agents must be diluted before being used, so conduct dilution under
the instruction of manufacturers;
3. Do not use any erosive material (such as steel wool or polishing agent);
4. Prevent the ingress of any liquid to the enclosure and any part of the device;
5. Ensure no residue of cleaning liquid on the surface of the device.
6.3 Cleaning Reagent

1. Diluted aqua ammonia
2. Diluted sodium hypochlorite (bleaching powder for washing)
3. Diluted formaldehyde 35 – 37%
4. Hydrogen peroxide 3%
5. Ethanol
6-1
Maintenance and Cleaning
6. Isopropyl alcohol
6.4 Sterilization
To avoid the long-time damage to the patient monitor, we recommend you
ü To conduct only sterilization which is considered necessary in your maintenance
plan;
ü To clean the patient monitor before the sterilization;
ü To sterilize the patient monitor with specified sterilization agent: Ethylate, and
Acetaldehyde.
For the sterilization agents of the ECG leads and blood pressure cuffs, refer to relevant
Operation Manual.
Caution
n Conduct dilution or use the liquid of the possibly-lowest concentration

under the instructions by the manufacturer.
n Prevent the ingress of liquid to the enclosure.
n Prevent any part of the system from being dipped.
n In sterilization, do not spill the liquid to the patient monitor.
n Ensure no residue of sterilization agent on the surface of the patient
monitor. Clean it if any.
6.5 Disinfection
To avoid the long-time damage to the patient monitor, we recommend you
ü To conduct only disinfection which is considered necessary in your maintenance
plan;
ü To clean the patient monitor before the disinfection;
For the disinfections of ECG leads, SpO2 sensor, blood pressure cuffs and temperature
sensor, refer to relevant Operation Manual.
Gas (EtO) or formaldehyde are forbidden for the disinfection of the patient
monitor.
6-2
P/N: 9100-20-11310(2.0)

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PM-9000 Super

SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD. (hereinafter called Mindray)

and are the registered trademarks or trademarks owned by Mindray in

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

This warranty shall not extend to

1. Obtain a return authorization.

Manufacturer: Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

Tel: +86 755 26522479 +86 755 26582888

Fax: +86 755 26582500 +86 755 26582501

EC Representative: Shanghai International Holding Corp. GmbH (Europe)

Address: Eiffestraße 80, 20537 Hamburg Germany

Signal word Meaning

Indicates an imminently hazardous situation which, if not

Indicates a potentially hazardous situation which, if not

Indicates a potentially hazardous situation which, if not

2. Meaning of Safety Symbols

Type-BF applied part

"Attention" (Refer to the operation manual.)

DANGER: Do not use flammable gases such as anesthetics, or flammable

liquids such as ethanol, near this product, because there is danger of

and fuses that control current to devices such as life-support

(1) Use of radio-wave-emitting devices in the proximity of this kind

2. Do not allow fluids such as water to contact the system or

Be Careful Protective earth ground

Indicates that the instrument is IEC-60601-1 Type CF equipment. The unit

Equipotential grounding terminal CE mark 93/42/EEC a directive

Silence Symbol ！ Close all alarm volume

@ Mark Event 》 Next menu

*** Highest level alarm ** Middle level alarm

* Lowest level alarm Alarm pause

Ð Trend graph cursor u SYS pressure（NIBP trend graph）

t DIA pressure(NIBP trend graph) * MEAN pressure (NIBP trend graph)

Î Right moving indicator Í Left moving indicator

Heart beat Pace signal

× Gain magnify √ Confirm

1.1 INTRODUCTION ...............................................................................................................................1

2.1 GENERAL ........................................................................................................................................1

CHAPTER 3 PRODUCT SPECIFICATIONS ......................................................................................1

3.1 SAFETY C LASSIFICATIONS ...............................................................................................................1

CHAPTER 4 DISASSEMBLING/ASSEMBLING & TROUBLESHOOTING ..................................1

4.1 PM-9000 EXPRESS DISASSEMBLING/ASSEMBLING ......................................................................1

CHAPTER 5 TEST AND MATERIAL LIST .........................................................................................1

5.1 TEST PROCEDURE .........................................................................................................................1

CHAPTER 6 MAINTENANCE AND CLEANING.................................................................................1

6.1 MAINTENANCE ...............................................................................................................................1

Chapter 1 About the Product

PM-9000 Super patient monitor has the following functions:

CH1: SYS, DIA

1.3.3 Electrical specification

4.4Ah 11.1V lithium battery

FOR YOUR NOTES

Figure 2-1 Structure of the PM-9000 Super

2.1.1 Parameter Measurement

2.1.2 Main Control Part

2.1.3 Man-Machine Interface

The speaker provides the auditory alarm function.

* Highest level alarm Middle level alarm