PM-9000 Express
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PM-9000 Express
Patient Monitor
Operation Manual
I
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.
© 2005 Shenzhen Mindray Bio-Medical Electronics Co., Ltd. All rights reserved.
II
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:
! All installation operations, expansions, changes, modifications and repairs of
this product are conducted by Mindray authorized personnel; and
! The electrical installation of the relevant room complies with the applicable
national and local requirements; and
! 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
! Any Mindray product which has been subjected to misuse, negligence or
accident; or
! Any Mindray product from which Mindray's original serial number tag or
product identification markings have been altered or removed; or
! Any product of any other manufacturer.
III
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.
IV
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
V
Contents
Intellectual Property Statement.............................................................................I
Manufacturer’s Responsibility..............................................................................II
Warranty......................................................................................................... II
Exemptions..................................................................................................... II
Return Policy........................................................................................................III
Contact Information ............................................................................................ IV
Contents ..................................................................................................................V
Preface......................................................................................................................1
Manual Purpose...............................................................................................1
Intended Audience...........................................................................................1
Version Information ........................................................................................1
Illustrations and Names...................................................................................2
Conventions ....................................................................................................2
1 Safety.................................................................................................................... 1-1
1.1 Safety Information ...................................................................................... 1-2
1.1.1 Dangers ........................................................................................... 1-3
1.1.2 Warnings.......................................................................................... 1-3
1.1.3 Cautions........................................................................................... 1-4
1.1.4 Notes ............................................................................................... 1-5
1.2 Equipment Symbols .................................................................................... 1-6
1.3 CE Marking................................................................................................. 1-8
1.4 Reference Literature.................................................................................... 1-9
2 The Basics............................................................................................................ 2-1
2.1 Monitor Description .................................................................................... 2-2
Contents
VI
2.1.1 Intended Use.................................................................................... 2-2
2.1.2 Contraindications ............................................................................ 2-3
2.1.3 Components..................................................................................... 2-3
2.1.4 Functions......................................................................................... 2-3
2.2 External Appearance ................................................................................... 2-5
2.2.1 Front Panel ...................................................................................... 2-5
2.2.2 Side Panel........................................................................................ 2-6
2.2.3 Rear Panel ....................................................................................... 2-8
2.3 Control Panel............................................................................................. 2-10
2.4 Display ...................................................................................................... 2-12
2.5 Batteries .................................................................................................... 2-15
2.5.1 Battery Maintenance ..................................................................... 2-16
2.5.2 Battery Recycling.......................................................................... 2-17
3 Installation and Maintenance............................................................................. 3-1
3.1 Installation................................................................................................... 3-2
3.1.1 Unpacking and Checking ................................................................ 3-2
3.1.2 Environmental Requirements.......................................................... 3-3
3.1.3 Power Source Requirements ........................................................... 3-3
3.1.4 Bracket Mounting............................................................................ 3-3
3.1.5 Installation Method ......................................................................... 3-4
3.1.6 Powering on the Monitor................................................................. 3-8
3.1.7 Powering off the Monitor................................................................ 3-8
3.2 Maintenance ................................................................................................ 3-9
3.2.1 Inspection ........................................................................................ 3-9
3.2.2 Cleaning ........................................................................................ 3-10
3.2.3 Disinfection and Sterilization.........................................................3-11
4 System Menu ....................................................................................................... 4-1
4.1 Overview..................................................................................................... 4-2
4.2 Patient Setup................................................................................................ 4-4
4.2.1 Admit Patient .................................................................................. 4-5
4.2.2 Quick Admit Patient ........................................................................ 4-7
4.2.3 Modify Patient................................................................................. 4-7
4.2.4 Discharge Patient............................................................................. 4-7
4.3 Default Setup............................................................................................... 4-9
4.4 System Setup ............................................................................................. 4-10
4.4.1 Face Select .....................................................................................4-11
Contents
VII
4.4.2 Alarm Setup .................................................................................. 4-12
4.4.3 Time Setup .................................................................................... 4-13
4.4.4 Recorder Setup .............................................................................. 4-14
4.4.5 Data Output ................................................................................... 4-16
4.4.6 Analog Output............................................................................... 4-17
4.4.7 Module Setup ................................................................................ 4-18
4.4.8 Trace Setup.................................................................................... 4-19
4.4.9 Mark Event.................................................................................... 4-20
4.5 Selection Setup.......................................................................................... 4-21
4.6 Monitor Version ........................................................................................ 4-22
4.7 Maintenance .............................................................................................. 4-24
4.7.1 IP Address Setup ........................................................................... 4-27
4.7.2 Wireless Net Setup ........................................................................ 4-27
4.7.3 Self Definition of Color................................................................. 4-28
4.7.4 Nurse Call Setup ........................................................................... 4-29
4.7.5 CO
2
User Maintain........................................................................ 4-31
4.7.6 Monitor Status............................................................................... 4-31
4.8 DEMO Function........................................................................................ 4-32
5 Face Selection ...................................................................................................... 5-1
5.1 Standard Screen........................................................................................... 5-2
5.2 Trend Screen ............................................................................................... 5-3
5.3 OxyCRG Screen.......................................................................................... 5-4
5.4 Viewbed Screen........................................................................................... 5-5
5.5 Large Font Screen ....................................................................................... 5-8
5.6 Standby Mode ............................................................................................. 5-9
6 Alarms.................................................................................................................. 6-1
6.1 Overview..................................................................................................... 6-2
6.1.1 Alarm Categories............................................................................. 6-2
6.1.2 Alarm Levels................................................................................... 6-3
6.2 Alarm Modes............................................................................................... 6-4
6.2.1 Visual Alarms.................................................................................. 6-4
6.2.2 Audible alarms ................................................................................ 6-4
6.2.3 Alarm Messages .............................................................................. 6-5
6.2.4 Parameter Flashes............................................................................ 6-5
6.3 Alarm Statuses ............................................................................................ 6-6
6.3.1 Alarms Disabled.............................................................................. 6-6
Contents
VIII
6.3.2 Alarms Paused................................................................................. 6-7
6.3.3 System Silenced .............................................................................. 6-7
6.3.4 Alarms Silenced .............................................................................. 6-7
6.3.5 Status Switchover............................................................................ 6-8
6.4 Latching Alarms.......................................................................................... 6-9
6.5 Clearing Alarms ........................................................................................ 6-10
6.6 When an Alarm Occurs ..............................................................................6-11
7 Freezing Waveforms........................................................................................... 7-1
7.1 Overview..................................................................................................... 7-2
7.2 Freezing and Unfreezing ............................................................................. 7-2
7.3 FROZEN Menu........................................................................................... 7-3
7.4 Waveform Recall ......................................................................................... 7-4
7.5 Recording Frozen Waveforms..................................................................... 7-4
8 Recording............................................................................................................. 8-1
8.1 Overview..................................................................................................... 8-2
8.2 Recording Types.......................................................................................... 8-2
8.3 Recorder Operations.................................................................................... 8-5
8.4 Installing Recorder Paper ............................................................................ 8-9
9 Recall.................................................................................................................... 9-1
9.1 Overview..................................................................................................... 9-2
9.2 Trend Graph Recall ..................................................................................... 9-3
9.3 Trend Table Recall ...................................................................................... 9-5
9.4 NIBP Recall................................................................................................. 9-7
9.5 Alarm Event Recall ..................................................................................... 9-8
9.6 Non-Volatile Data Storage......................................................................... 9-10
10 Drug Calculation............................................................................................... 10-1
10.1 Drug Calculation ....................................................................................... 10-2
10.2 Titration Table ........................................................................................... 10-5
Contents
IX
11 ECG/RESP Monitoring.................................................................................... 11-1
11.1 Overview....................................................................................................11-2
11.1.1 ECG Waveform ..............................................................................11-2
11.1.2 ECG Parameters .............................................................................11-4
11.2 ECG Monitoring Procedure .......................................................................11-5
11.2.1 Preparation .....................................................................................11-5
11.2.2 Electrode Placement.......................................................................11-6
11.3 ECG Setup Menu .....................................................................................11-12
11.4 ST Analysis ..............................................................................................11-20
11.4.1 Overview......................................................................................11-20
11.4.2 ST Analysis Menu ........................................................................11-20
11.5 Arrhythmia Analysis ................................................................................11-24
11.5.1 Overview......................................................................................11-24
11.5.2 Arrhythmia Analysis Menu ..........................................................11-25
11.5.3 Arrhythmia Alarm Setup ..............................................................11-26
11.5.4 Arrhythmia Recall ........................................................................11-27
11.6 ECG 12-Lead Monitoring ........................................................................11-29
11.6.1 General.........................................................................................11-29
11.6.2 Monitoring Procedure ..................................................................11-30
11.6.3 ECG Setup Menu for 12-Lead Monitoring ..................................11-33
11.6.4 Data Review .................................................................................11-40
11.7 RESP Monitoring .....................................................................................11-42
11.7.1 Overview......................................................................................11-42
11.7.2 Electrode Placement.....................................................................11-43
11.7.3 Respiration Setup .........................................................................11-44
11.8 Maintenance and Cleaning .......................................................................11-46
12 SpO
2
Monitoring............................................................................................... 12-1
12.1 Overview................................................................................................... 12-2
12.2 Mindray SpO
2
Module .............................................................................. 12-4
12.2.1 Principles of Operation.................................................................. 12-4
12.2.2 Precautions .................................................................................... 12-5
12.2.3 Monitoring Procedure ................................................................... 12-6
12.2.4 Measurement Limitations.............................................................. 12-8
12.2.5 SpO
2
Setup Menu.......................................................................... 12-9
12.3 Masimo SpO
2
Module............................................................................. 12-12
12.3.1 Principles of Operation................................................................ 12-12
12.3.2 Precautions .................................................................................. 12-14
Contents
X
12.3.3 Monitoring Procedure ................................................................. 12-16
12.3.4 Measurement Limitations............................................................ 12-16
12.3.5 SpO
2
Setup Menu........................................................................ 12-17
12.3.6 Sensors and Accessories.............................................................. 12-19
12.3.7 Masimo Information.................................................................... 12-22
12.4 Nellcor SpO
2
Module.............................................................................. 12-23
12.4.1 Principles of Operation................................................................ 12-23
12.4.2 Precautions .................................................................................. 12-25
12.4.3 Monitoring Procedure ................................................................. 12-26
12.4.4 Measurement Limitations............................................................ 12-27
12.4.5 SpO
2
Setup Menu........................................................................ 12-28
12.4.6 Accessories.................................................................................. 12-30
12.4.7 Nellcor Information..................................................................... 12-32
13 NIBP Monitoring............................................................................................... 13-1
13.1 Overview................................................................................................... 13-2
13.2 Monitoring Procedure ............................................................................... 13-3
13.2.1 Cuff Selection and Placement ....................................................... 13-3
13.2.2 Operation Guides........................................................................... 13-4
13.3 Measurement Limitations.......................................................................... 13-6
13.4 NIBP Setup Menu ..................................................................................... 13-7
13.4.1 Calibration..................................................................................... 13-9
13.4.2 Testing for Air Leakage............................................................... 13-10
13.5 Maintenance and Cleaning .......................................................................13-11
14 TEMP Monitoring............................................................................................. 14-1
14.1 Overview................................................................................................... 14-2
14.2 Measurement Procedure ............................................................................ 14-3
14.3 TEMP Setup Menu.................................................................................... 14-4
14.4 Maintenance and Cleaning ........................................................................ 14-6
15 IBP Monitoring ................................................................................................. 15-1
15.1 Overview................................................................................................... 15-2
15.2 Precautions ................................................................................................ 15-3
15.3 Monitoring Procedure ............................................................................... 15-4
Contents
XI
15.4 IBP Menu .................................................................................................. 15-5
15.4.1 IBP Setup Menu ............................................................................ 15-5
15.4.2 IBP Pressure Zero Menu ............................................................... 15-8
15.4.3 IBP Pressure Calibration ..............................................................15-11
15.5 Maintenance and Cleaning ...................................................................... 15-14
15.6 ICP Transducer ICT/B............................................................................. 15-16
15.6.1 Introduction ................................................................................. 15-16
15.6.2 Precautions .................................................................................. 15-17
15.6.3 Calibration and Zeroing .............................................................. 15-18
15.6.4 Application of ICT/B .................................................................. 15-20
15.6.5 Maintenance and Cleaning .......................................................... 15-23
15.6.6 Frequently Asked Questions........................................................ 15-26
16 CO Monitoring.................................................................................................. 16-1
16.1 Overview................................................................................................... 16-2
16.2 Measurement Procedure ............................................................................ 16-3
16.2.1 Window for CO Measurement ...................................................... 16-5
16.2.2 Blood Temperature Monitoring..................................................... 16-8
16.3 CO Setup Menu......................................................................................... 16-9
16.4 Hemodynamic Calculation .......................................................................16-11
16.5 Maintenance and Cleaning ...................................................................... 16-13
17 CO
2
Monitoring................................................................................................. 17-1
17.1 Overview................................................................................................... 17-2
17.2 Mindray CO
2
Module................................................................................ 17-3
17.2.1 Principles of Operation.................................................................. 17-3
17.2.2 Preparations for CO
2
Measurement............................................... 17-4
17.2.3 CO
2
Setup Menu ........................................................................... 17-6
17.2.4 CO
2
User Maintain Menu............................................................ 17-10
17.2.5 Maintenance and Cleaning .......................................................... 17-12
17.3 Oridion CO
2
Module ............................................................................... 17-13
17.3.1 Principles of Operation................................................................ 17-13
17.3.2 Preparations for CO
2
Measurement............................................. 17-14
17.3.3 CO
2
Setup Menu ......................................................................... 17-15
17.3.4 CO
2
User Maintain Menu............................................................ 17-19
17.3.5 Maintenance and Cleaning .......................................................... 17-21
17.3.6 Oridion Information .................................................................... 17-21
17.4 Welch Allyn CO
2
Module ....................................................................... 17-22
Contents
XII
17.4.1 Principles of Operation................................................................ 17-22
17.4.2 Preparations for CO
2
Measurement............................................. 17-23
17.4.3 CO
2
Setup Menu ......................................................................... 17-24
17.4.4 Maintenance and Cleaning .......................................................... 17-28
18 Anesthesia Gas Monitoring.............................................................................. 18-1
18.1 Overview................................................................................................... 18-2
18.2 Measurement Principles and Procedure .................................................... 18-4
18.3 AG Setup Menu......................................................................................... 18-6
18.4 Maintenance and Cleaning ...................................................................... 18-10
19 Accessories......................................................................................................... 19-1
19.1 ECG Accessories....................................................................................... 19-2
19.2 SpO
2
Accessories ...................................................................................... 19-4
19.2.1 Mindray SpO
2
Accessories............................................................ 19-4
19.2.2 Masimo SpO
2
Accessories ............................................................ 19-5
19.2.3 Nellcor SpO
2
Accessories.............................................................. 19-5
19.3 NIBP Accessories ...................................................................................... 19-6
19.4 TEMP Accessories .................................................................................... 19-7
19.5 IBP Accessories......................................................................................... 19-8
19.6 CO Accessories ......................................................................................... 19-9
19.7 CO
2
Accessories...................................................................................... 19-10
19.7.1 Mindray CO
2
Accessories ........................................................... 19-10
19.7.2 Oridion CO
2
Accessories............................................................. 19-10
19.7.3 Welch Allyn CO
2
Accessories ......................................................19-11
19.8 AG Accessories ....................................................................................... 19-12
20 Appendices......................................................................................................... 20-1
Appendix A Product Specifications................................................................. 20-2
A.1 Safety Classifications .................................................................... 20-2
A.2 Environmental Specifications........................................................ 20-3
A.3 Power Source Specifications......................................................... 20-4
A.4 Hardware Specifications ............................................................... 20-5
A.5 Wireless network........................................................................... 20-6
A.6 Data Storage .................................................................................. 20-6
Contents
XIII
A.7 Signal Output Specifications......................................................... 20-7
A.8 ECG Specifications ....................................................................... 20-8
A.9 RESP Specifications.................................................................... 20-10
A.10 SpO
2
Specifications......................................................................20-11
A.11 NIBP Specifications .................................................................... 20-13
A.12 TEMP Specifications................................................................... 20-14
A.13 IBP Specifications ....................................................................... 20-15
A.14 CO Specifications........................................................................ 20-16
A.15 CO
2
Specifications ...................................................................... 20-17
A.16 AG Specifications ....................................................................... 20-20
Appendix B EMC .......................................................................................... 20-22
Appendix C Alarm Messages and Prompt Information................................. 20-27
C.1 Physiological Alarm Messages.................................................... 20-27
C.2 Technical Alarm Messages.......................................................... 20-28
C.3 Prompt Messages......................................................................... 20-40
Appendix D Optional Functions.................................................................... 20-43
Appendix E Symbols and Abbreviations....................................................... 20-45
E.1 Symbols....................................................................................... 20-45
E.2 Abbreviations .............................................................................. 20-47
Contents
XIV
FOR YOUR NOTES
1
Preface
Manual Purpose
This manual provides the instructions necessary to operate the PM-9000 Express
Patient Monitor (hereinafter called as this monitor) in accordance with its function
and intended use. Observance of this manual is a prerequisite for proper
performance and correct operation, and ensures patient and operator safety.
This manual is written based on the maximum configuration. Part of this manual
may not apply to your monitor. If you have any question about the configuration of
your monitor, please contact our Customer Service.
This manual is an integral part of and should always be kept close to the patient
monitor, so that it can be obtained conveniently when necessary.
Intended Audience
This manual is geared for the clinical medical professionals. Clinical medical
professionals are expected to have working knowledge of medical procedures,
practices and terminology as required for monitoring of critically ill patients.
Version Information
This manual has a version number. This version number changes whenever the
manual is updated due to software or technical specification change. Content of this
manual is subject to change without prior notice. The version information of this
manual is as follows.
Version number Release date
2.0 2005-11-1
Preface
2
Illustrations and Names
All illustrations in this manual are provided as examples only. They may not
necessarily accord with the graph, settings or data displayed on your patient monitor.
All names appeared in this manual and illustrations are fictive. It is a mere
coincidence if the name is the same with yours.
Conventions
! Italic text is used in this manual to quote the referenced chapters or sections.
! The terms danger, warning, and caution are used throughout this manual to point
out hazards and to designate a degree or level or seriousness.
1-1
1 Safety
1.1 Safety Information ...................................................................................... 1-2
1.1.1 Dangers ........................................................................................... 1-3
1.1.2 Warnings.......................................................................................... 1-3
1.1.3 Cautions........................................................................................... 1-4
1.1.4 Notes ............................................................................................... 1-5
1.2 Equipment Symbols .................................................................................... 1-6
1.3 CE Marking................................................................................................. 1-8
1.4 Reference Literature.................................................................................... 1-9
Safety
1-2
1.1 Safety Information
The safety statements presented in this chapter refer to the basic safety information
that the operator of the patient monitor shall pay attention to and abide by. There are
additional safety statements in other chapters or sections, which may be the same as
or similar to the followings, or specific to the operations.
DANGER
# Indicates an imminent hazard situation that, if not avoided, will result in
death or serious injury.
WARNING
# Indicates a potential hazard situation or unsafe practice that, if not
avoided, could result in death or serious injury.
CAUTION
# Indicates a potential hazard or unsafe practice that, if not avoided, could
result in minor personal injury or product/property damage.
NOTE
# Provides application tips or other useful information to ensure that you
get the most from your product.
Safety
1-3
1.1.1 Dangers
There are no dangers that refer to the product in general. Specific “Danger”
statements may be given in the respective sections of this operation manual.
1.1.2 Warnings
WARNING
# The device is intended for use by qualified clinical physicians or
well-trained nurses in the specified places.
# To ensure patient safety, verify the device and accessories can function
safely and normally before use.
# EXPLOSION HAZARD: Do not use this device in the presence of
flammable anesthetics, explosive substances, vapors or liquids.
# You must customize the alarm settings according to the individual
patient situation, and make sure the alarm sound is activated when an
alarm occurs.
# ELECTRIC SHOCK: Do not open the monitor housing. All servicing and
future upgrades to this device must be carried out by personnel trained
and authorized by our company only.
# DEFIBRILLATION: Do not come into contact with the patient during
defibrillation. Otherwise serious injury or death could result.
# When used in conjunction with electro-surgery equipment, you must
give top priority to the patient safety.
# DISPOSE: Dispose of the package material, observing the applicable
waste control regulations and keeping it out of children’s reach.
# The device must be connected to a properly installed power outlet with
protective earth contacts only. If the installation does not provide for a
protective earth conductor, disconnect the monitor from the power line
and operate it on battery power, if possible.
Safety
1-4
1.1.3 Cautions
CAUTION
# To ensure patient safety, use only parts and accessories specified in this
manual.
# Remove the battery from the patient monitor if it will not be used or not
be connected to the power line for a long period.
# Disposable devices are intended for single use only. They should not be
reused as performance could degrade or contamination could occur.
# At the end of its service life, the product described in this manual, as
well as its accessories, must be disposed of in compliance with the
guidelines regulating the disposal of such products. If you have any
questions concerning disposal of the products, please contact with us.
# Magnetic and electrical fields are capable of interfering with the proper
performance of the device. For this reason make sure that all external
devices operated in the vicinity of the monitor comply with the relevant
EMC requirements. Mobile phone, X-ray equipment or MRI devices are a
possible source of interference as they may emit higher levels of
electromagnetic radiation.
# Before connecting the patient monitor to the power line, check that the
voltage and frequency ratings of the power line are the same as those
indicated on the label or in this manual.
# Install or carry the patient monitor properly to avoid damages caused by
drop, impact, strong vibration or other mechanical force.
Safety
1-5
1.1.4 Notes
NOTE
# Keep this manual close to the patient monitor so that it can be obtained
conveniently when necessary.
# This patient monitor complies with the requirements of CISPR11
(EN55011) class A.
# The software was developed per IEC601-1-4. The possibility of hazards
arising from errors in software program is minimized.
# Put the patient monitor in a location where you can easily see the screen
and access the operating controls.
# The instructions of this manual are based on the maximum
configuration. Some of them may not apply to your patient monitor.
Safety
1-6
1.2 Equipment Symbols
NOTE
# Some symbols may not appear on all equipment.
Attention: Consult accompanying documents (this manual).
Power ON/OFF
Alternating current (AC)
Battery indicator
Type CF applied part. The unit displaying this symbol contains
an F-type isolated (floating) patient part providing a high
degree of protection against shock, and is suitable for use
during defibrillation.
TYPE BF applied part. Defibrillator-proof protection against
electrical shock.
Equipotentiality
Gas inlet
Gas outlet
Auxiliary output
Network connector
VGA connector
Safety
1-7
Manufacture date
Serial number
European community representative
This mark means that this device is fully in conformance with
the Council Directive Concerning Medical Devices 93/42/EEC.
The number adjacent to the CE marking (0123) is the number
of the EU-notified body that certified meeting the requirements
of Annex II of the Directive.
The following definition of the WEEE label applies to EU
member states only.
This symbol indicates that this product should not be treated as
household waste. By ensuring that this product is disposed of
correctly, you will help prevent bringing potential negative
consequences to the environment and human health. For more
detailed information with regard to returning and recycling this
product, please consult the distributor from whom you
purchased it.
* For system products, this label may be attached to the main
unit only.
Safety
1-8
1.3 CE Marking
The patient monitor bears CE mark indicating its conformity with the provision of
Council Directive 93/42/EEC concerning medical devices, and fulfills the essential
requirement of Annex I of this directive.
The patient monitor is in radio-interference protection class A in accordance with
EN55011.
The product complies with the requirement of standard EN60601-1-2
“Electromagnetic Compatibility – Medical Electrical Equipment”.
Safety
1-9
1.4 Reference Literature
1. Medical Device Directive 93/42/EEC
2. EN60601-1+A1+A2 or IEC60601-1+A1+A2, Medical Electrical Equipment,
Part 1: General Requirements for Safety
3. EN60601-1-1 or IEC60601-1-1, Medical Electrical Equipment- Part 1-1:
General Requirements for Safety - Collateral Standard: Safety Requirements
for Medical Electrical Systems
4. IEC60601-1-4, Medical Electrical Equipment- Part 1-4: General Requirements
for Safety - Collateral Standard: Programmable Electrical Medical Systems
5. IEC60601-2-49 Medical Electrical Equipment-Part 2-49: Particular
Requirements for the Safety of Multifunction Patient Monitoring Equipment
Safety
1-10
FOR YOUR NOTES
2-1
2 The Basics
2.1 Monitor Description .................................................................................... 2-2
2.1.1 Intended Use.................................................................................... 2-2
2.1.2 Contraindications ............................................................................ 2-3
2.1.3 Components..................................................................................... 2-3
2.1.4 Functions......................................................................................... 2-3
2.2 External Appearance ................................................................................... 2-5
2.2.1 Front Panel ...................................................................................... 2-5
2.2.2 Side Panel........................................................................................ 2-6
2.2.3 Rear Panel ....................................................................................... 2-8
2.3 Control Panel............................................................................................. 2-10
2.4 Display ...................................................................................................... 2-12
2.5 Batteries .................................................................................................... 2-15
2.5.1 Battery Maintenance ..................................................................... 2-16
2.5.2 Battery Recycling.......................................................................... 2-17
The Basics
2-2
2.1 Monitor Description
This monitor integrates the functions of parameter measurement, waveform
monitoring, freezing, and recording, etc. Its color TFT liquid crystal display is able
to show patient parameters and waveforms clearly. The monitor also features
compact size, lightweight, easy-to-carry handle and built-in battery, which make it
portable, especially in hospital transport. The compact control panel and control
knob, and the easy-to-use menu system enable you to freeze, record, or perform
other operations conveniently. Besides, this monitor can be connected with the
central monitoring system whereby a monitoring network will be formed.
2.1.1 Intended Use
The intended use of this monitor is to monitor a fixed set of parameters (see 2.1.4
Functions) for single adult, pediatric and neonatal patient, to display patient data
and waveforms, to store patient data in a trend database, and to generate alarms and
recordings.
This monitor is to be used in but not restricted to medical institutions such as ICU,
CCU, cardiopathy ICU, operating room, emergency room and postoperative
observation ward etc. This monitor may also be used during hospital transport or
ambulance. This monitor is not intended for helicopter transport or home use.
WARNING
# This Monitor is to be operated by clinical physicians or appropriate
medical staffs under the direction of physicians. The operator of the
monitor must be well trained. Any operation by unauthorized or
non-trained personnel is forbidden.
# The physiological waveforms and parameters and the alarm information
displayed by the monitor are only for the reference of physicians, but
cannot be used directly to determine the clinical treatment.
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