Product Information

 Product Model: M850

 Product Name: Patient monitor
 Manufacturer: Guangdong Biolight Meditech Co., Ltd.
 After Service Contact Information:
Address: No.2 Innovation First Road, Technical
Innovation Coast, Hi-tech Zone, Zhuhai, P.R.
China
Fax: +86-756-3399919
Postcode: 519085
Toll-free consultation hot line: +86-400-8818-233

Revision History
This manual has a revision number. This revision
number changes whenever the manual is updated due to
software or technical specification change. Contents of this
manual are subject to change without prior notice.
 Document No.: J/M850CE-A-008
 Revision number: V1.0
 Release time: Feb. 2017
Copyright © 2017 Guangdong Biolight Meditech Co., Ltd.
All rights reserved.

I
CE mark

ve Name:
EC Representativ
Shanghai International Holding Corp. GmbH (Europ
pe)
ve Address:
EC Representativ
Eiffestraβe 80, 20537 Hamburg Germany

Statement
Manufacturer holds the copyright of this manuaal, and we
o deal with this manual as confideential files.
are also entitled to
This manual is only
o used for operation, mainten
nance and
service of productt, someone else can not publish thee manual.
This manual contains
c exclusive information pro
otected by
copyright laws an
nd we reserve its copyright. Withou
ut written
approval of manu
ufacturer no parts of this manuall shall be
photocopied, xero
oxed or translated into other languaages.
The contents contained in this manual are subject
s to
amendments without notification.

Manufactureer's Responsibility
Only under the following circumstancces will

II
manufacturer be responsible for the safety, reliability and
performance of the instrument:
 All the installation, expansion, readjustment, renovation
or repairs are conducted by the personnel certified by
manufacturer.
 The storage condition, operation condition and electrical
status of the instrument conform to the product
specification.
 The instrument is used in accordance with the user’s
manual.
About this manual
This manual contains the instructions necessary to
operate the product safely and in accordance with its
function and intended use. Observance of this manual is a
prerequisite for proper product performance and correct
operation and ensures patient and operator safety.
This manual is based on the maximum configuration and
therefore some contents may not apply to your product. If
you have any question, please contact us.
This manual is an integral part of the product. It should
always be kept close to the equipment so that it can be
obtained conveniently when needed.
All illustrations in this manual serve as examples only.

III
They may not necessarily reflect the setup or data displayed
on your product.
Conventions:
 Bold Italic text is used in this manual to quote
the referenced chapter or sections.
 【】is used to enclose screen texts.
 → is used to indicate operational procedures.
Signs in this manual:

 Warning: Indicates a potential hazard or unsafe

practice that, if not avoided, will 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.

IV
 Contents
Chapter 1 General Introduction........................................... 1-1 
1.1  Intended Use .............................................................. 1-1 
1.2  Main Unit ................................................................... 1-2 
1.3  Display Views ............................................................ 1-7 
Chapter 2 Safety ..................................................................... 2-1 
2.1  Safety Information ..................................................... 2-1 
2.2  Explanation of Symbols ............................................ 2-5 
Chapter 3 Basic Operations .................................................. 3-1 
3.1  Unpacking and Checking .......................................... 3-1 
3.2  Getting Started ........................................................... 3-1 
3.3  Starting the Monitor .................................................. 3-2 
3.4  Screen Brightness Setting .......................................... 3-2 
3.5  Auto-Rotate Setting ................................................... 3-3 
3.6  Date & Time Setting.................................................. 3-3 
3.7  Patient Information Setting ....................................... 3-4 
3.8  Demo Mode Setting................................................... 3-4 
3.9  Language Setting ....................................................... 3-5 
3.10 Checking the Version ................................................ 3-5 
3.11 Restoring the Factory Configuration ......................... 3-6 
3.12 Shutting off the Monitor ............................................ 3-6 
Chapter 4 Alarm .................................................................... 4-1 
4.1  Alarm Categories ....................................................... 4-2 

V
 4.2  Alarm Levels ............................................................. 4-2 
4.3  Alarm Indicators ........................................................ 4-4 
4.4  Alarm Status Symbol................................................. 4-7 
4.5  Alarm Tone Configuration ........................................ 4-7 
4.6  Pausing Alarms .......................................................... 4-8 
4.7  Adjust the Alarm Volume to Zero ............................. 4-9 
4.8  Alarm Reset ............................................................. 4-10 
4.9  When an Alarm Occurs ........................................... 4-11 
Chapter 5 Measuring ECG ................................................... 5-1 
5.1  Introduction ............................................................... 5-1 
5.2  Safety Information ..................................................... 5-1 
5.3  Monitoring Procedure................................................ 5-3 
5.4  Checking Paced Status .............................................. 5-8 
5.5  ECG Display ............................................................ 5-10 
5.6  Setting ECG ............................................................. 5-10 
Chapter 6 Measuring RESP ................................................. 6-1 
6.1  Principle of Measuring .............................................. 6-1 
6.2  Preparatory Steps of Measurement ........................... 6-1 
6.3  Resp Display .............................................................. 6-3 
6.4  Resp Setup ................................................................. 6-3 
Chapter 7 Measuring SpO2 .................................................. 7-1 
7.1  Introduction ............................................................... 7-1 
7.2  Safety Information ..................................................... 7-2 

VI
 7.3  Monitoring Procedure................................................ 7-4 
7.4  SpO2 Display............................................................. 7-5 
7.5  PR Display ................................................................. 7-6 
7.6  SpO2 Setup ................................................................ 7-7 
7.7  Desat limit Setup ....................................................... 7-9 
Chapter 8 Trend Review ....................................................... 8-1 
8.1  Introduction ............................................................... 8-1 
8.2  Review Interface ........................................................ 8-1 
8.3  Review Setup ............................................................. 8-2 
Chapter 9 Battery .................................................................. 9-1 
9.1  Introduction ............................................................... 9-1 
9.2  Charging the Battery.................................................. 9-2 
9.3  Optimizing Battery Performance .............................. 9-2 
9.4  Checking the Lithium Battery ................................... 9-3 
9.5  Disposing of the Batteries ......................................... 9-4 
Chapter 10 Maintenance and Cleaning ............................. 10-1 
10.1 Introduction ............................................................. 10-1 
10.2 Seasonal Safety Checking ....................................... 10-2 
10.3 Cleaning the Monitor............................................... 10-4 
10.4 Cleaning ECG Cable ............................................... 10-5 
10.5 Cleaning SpO2 Sensor............................................. 10-6 
10.6 Disposal ................................................................... 10-6 
Chapter 11 Accessories ........................................................ 11-1 

VII
Appendix A Product Specifications ......................................... 1 
A.1 Safety Specifications ..................................................... 1 
A.2 Physical Specifications .................................................. 2 
A.3 Environmental Specifications........................................ 2 
A.4 Charging Specifications................................................. 2 
A.5 Hardware Specifications................................................ 3 
A.6 Data Storage .................................................................. 4 
A.7 Measurement Specifications.......................................... 5 
Appendix B Factory Defaults ................................................ 13 
B.1 Alarm Setup ................................................................. 13 
B.2 System Setup................................................................ 13 
B.3 ECG Setup ................................................................... 14 
B.4 SpO2 Setup .................................................................. 14 
B.5 Trend Setup .................................................................. 14 
Appendix C Alarm Message .................................................. 15 
C.1 Physiological Alarm..................................................... 15 
C.2 Technical Alarm ........................................................... 16 
C.3 Prompt Message........................................................... 17 
Appendix D Guidance and Manufacturer’s Declaration of
EMC ......................................................................................... 18 
Appendix E Warranty Registration Card ............................ 27 

VIII
 Patient Monitor User’s Manual

Chapter 1 General Introduction

1.1 Intended Use

M850 Patient monitor is intended for continuously
monitoring or spot checking of SpO2, PR, ECG, HR and RR
parameters of single adult, pediatric and neonatal patient.
This device can be used in institutions or units with health care
capability. For instance, outpatient departments, emergency
rooms and departments of internal medicine in hospitals, and
ordinary departments in clinics, nursing hospitals and medical
institutions for communities.

 Warning: The monitor is intended for use only by

clinical professionals or under their
guidance. It must only be used by persons
who have received adequate training in its
use. Anyone unauthorized or untrained
must not perform any operations on it.

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1.2 Main Unitt

1.2.1 Front View

w

6 1

5 3
4

Fig 1--1 Front View of the Monitor

1. Alarm indicating lamp
When an alarrm occurs, this lamp will light up as defined
below:
 High level alaarm: the lamp quickly flashes red.
 Medium levell alarm: the lamp slowly flashes yeellow.

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 Patient Monitor User’s Manual

 Low level alarm: the lamp lights yellow without flashing.

2. Display screen
The device uses resistive touchscreen, using stylus or
fingernail will improve sensitivity.
3. Alarm pause button
 It can pause the alarm for 120s when alarm volume is on.
 Pressing it can change the alarm message to prompt
message when “Lead off” or “Sensor off” alarm happens.
4. Main interface button
 Press this button to return to main interface when it is on
menu setting.
 Press this button to shift between different display modes
when it is in main interface.
5. Menu
 Press this button to enter into menu interface when it is on
main interface.
 Press this button to return to main interface when it is on
menu setting interface.
6. Battery charging indicating lamp
 It is orange when the device is being charged.
 It turns off when the battery is full or device isn’t being
charged.

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1.2.2 Rear View

w

Fig 1--2 Rear View of the Monitor

1.2.3 Side View

Topside:

1 2

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 Patiient Monitor User’s Manual

Downside:

Rightside:

4 5

Fig 1-3 Side View of the Monitor

1. ECG cable connector
2. onnector
SpO2 probe co
3. Micro USB co
onnector
 Connect with power adapter.

Caution：Usse only power adapters specified in this

ma
anual. Using other power adap
pters may
cau
use damage, and the power ad
dapter is a
part of the product.

 o computer.
Export data to

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 Patient Monitor User’s Manual

 Warning:
 The equipment connected to monitor shall meets
requirements of the system standard IEC 60601-1. If
in doubt, consult the technical service department or
your local representative.
 Operator shall be responsible for safe of system after
monitor connected to computer.
 Don’t touch the patient when operating the USB
connector, if not, it will generate risk of electric shock.

4. Shortcut key
Press this button to freeze or unfreeze the ECG waveform
5. Power buttom
 Press it about two seconds to turn on when the monitor is
on the condition of shutdown.
 Press it about two seconds to turn off when the monitor is
on the condition of working.
 Calibration of touch screen
Press shortcut key firstly and press power button and
immediately loose shortcut key, click the center of
appearing point on screen. If the calibration passes, it will
enter the normall interface, if not, a red fork will appear
on screen and continue to calibrate.

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 Patient Monitor User’s Manual

1.3 Display Views

This device has a function of automatic display rotation

(Gravity Activated) which provides for vertical and horizontal
positioning to maximizing space utilization and visibility.

1.3.1 Multi-Parameter Display Mode

8
9
7

2 10

1 11
12
Fig 1-4 Multi-Parameter Display Mode

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 Patient Monitor User’s Manual

1. Patient ID No.: Click and then set patient information, its

range from 1 to 96.
2. HR parameter area: The current HR parameter and its
high and low alarm limits are shown in the area.
3. Resp waveform area: Resp waveform is shown in the
area.
4. ECG waveform area: ECG waveform is shown in the
area.
5. SpO2 parameter area: The current SpO2 and its high and
low alarm limits are shown in the area.
6. SpO2 waveform area: The waveform shown in the area is
current SpO2 volume curve.
7. Physiological alarm area: Current physiological alarm
information is shown in the area.
8. Technical alarm and prompt information area: Current
technical alarm and prompt information are shown in the
area.
9. Alarm status area: Alarm status symbols are shown in the
area.
10. Resp parameter area: The current Resp and its high and
low alarm limits are shown in the area.
11. System time: Current time is shown in the area.
12. Battery symbol: The symbol indicates the current quantity
of electricity of batteries and whether the device is

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 Patient Monitor User’s Manual

connecting power source, the alternating-current symbol

is above battery symbol when the device is connecting
power source.

1.3.2 SpO2 Display Mode

2 3

Fig 1-5 SpO2 Display Mode

1. SpO2 waveform area: The waveform shown in the area is
current SpO2 volume curve.
2. SpO2 parameter area: The values shown in the area are

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 Patient Monitor User’s Manual

current SpO2 value and its upper and lower alarm limits.
3. PR parameter area: The values shown in the area are
current PR value and its upper and lower alarm limits.

1.3.3 ECG Waveform Display Mode

Fig 1-6 ECG Display Mode

1. HR parameter area: The values shown in the area are
current HR value and its higher and lower alarm limits.

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 Patient Monitor User’s Manual

2. ECG waveform display area: Waveform shown in the area

is current ECG waveform.

1.3.4 ECG Waveform Display Mode with RESP

Fig 1-7 ECG Display Mode with RESP

1. ECG waveform display area: Waveform shown in the area
is current ECG waveform.
2. HR parameter area: The values shown in the area are
current HR value and its upper and lower alarm limits.

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 Patient Monitor User’s Manual

3. Resp waveform area: Resp waveform is shown in the

area.
4. Resp parameter area: The current Resp and its high and
low alarm limits are shown in the area.

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 Patient Monitor User’s Manual

Chapter 2 Safety

2.1 Safety Information


 Warning:
 Explosion hazard: Do not use the monitor in the
presence of flammable anesthetics mixture with air,
oxygen, or hydrogen.
 When the monitor is in use, there should not be any
great power appliances as high voltage cables, X-ray
machine, ultrasound equipment and electrizer in use
nearby.
 Do not open the monitor housings; electric shock
hazard may exist. All servicing and future upgrades
must be carried out by the personnel trained and
authorized by manufacturer only.
 Keep the monitor away from dust, vibration,
corrosive substances, explosive materials, high
temperature and moisture.
 Do not come into contact with the patient during
defibrillation. Otherwise serious injury or death could
result.
 When the monitor is connecting with high-frequency
devices, sensors and cables should avoid touching

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 Patient Monitor User’s Manual

high-frequency devices, in order to leakage current

burns patient.
 The monitor is not designed for the sterilized room.
 The monitor should be handled with care so as to
avoid shocks and falls.
 When the monitor is in use, it must be ensured the
batteries have sufficient capacity; otherwise there
might be such phenomena as starting-up
abnormalities or inaccurate measurement data, etc.
 For pacemaker patients, rate meters may continue to
count the pacemaker rate during occurrences of
cardiac arrest or some arrhythmias. Do not rely
entirely upon rate meter alarms. Keep pacemaker
patients under close surveillance.
 The use of accessories, sensors, and cables other than
those specified may result in increased emission, low
anti-disturbance and/or create invalid readings of the
monitor. It is advised to check it at least once a month.
 The physiological data and alarm messages displayed
on the monitor are for reference only and cannot be
directly used for diagnostic interpretation.
 Disposable devices are intended for single use only.
They should not be reused as performance could
degrade or contamination could occur.

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 Patient Monitor User’s Manual

 The service life of this monitor is five years. 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 questions
concerning disposal of products, please contact
manufacturer or its representatives.
 To avoid inadvertent disconnection, route all cables in
a way to prevent a stumbling hazard. Wrap and
secure excess cabling to avoid risk of entanglement or
strangulation by patient or personnel.
 The adapter plug is intended to be used as isolation
device from the supply mains. Please always make it
easily to operate.

Caution:
 The monitor does not contain any parts for self-repair
by users. The repair of the instrument must be
conducted by the technical personnel authorized by
manufacturer.
 To ensure patient safety, use only parts and
accessories specified in this manual.
 When the monitor is connected to AC power, the
battery is in a state of being recharged. When it is

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 Patient Monitor User’s Manual

unable to be connected to the AC power, the battery

can be used to supply power, and at this time it is
unnecessary to use the electrical wires, and the
instrument can be switched on directly.
 The monitor can only monitor one patient at a time.
 When a defibrillator is applied on a patient, the
monitor may have transient disorders in the display of
waveforms. If electrodes are used and placed properly,
the display of the monitor will be restored within 5s.
During defibrillation, please note to remove the
electrode of limb lead to the side of the limb.
 In order to have more accurate measurements results,
the monitor should be used in quiet and comfortable
environment.
 To guarantee the normal and safe operation of the
monitor, a preventive check and maintenance should
be conducted for the monitor and its parts every 6 to
12 months (including performance check and safety
check) to verify the instrument can work in a safe and
proper condition and it is safe to the medical
personnel and the patient and has met the accuracy
required by clinical use.
 This manual describes all features and options. Your
monitor may not have all of them.

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 Patiient Monitor User’s Manual

2.2 Explanattion of Symbols

Symbol Symbol Note

Type CF
C applied part, defibrillation proteected.

The uniit displaying this symbol contains an F-Type

isolated
d (floating) applied part providin
ng a high
degree of protection against shock
k, and is
defibrilllator-proof.

Refer to
o user’s manual.

Alternaating current

IPX1 Degree of protection against ingress of liq

quid

Alarm volume
v off

Alarm paused
p

Alarm reset
r

QRS vo
olume off

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 Patient Monitor User’s Manual

Date of manufacture

Manufacturer

Serial number

Power button

ECG Short for “Electrocardiogram”

SpO2 Short for “Pulse Oxygen Saturation”

Warning：the protection against the effects of the

discharge of a cardiac defibrillator is dependent
upon the appropriated cable
Contents of the distribution packages are fragile
therefore it shall be handled with care.
This is the correct upright position of the
distribution packages for the transport and/or
storage.
Distribution packages shall be kept away from rain
and be kept in dry conditions.

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 Patient Monitor User’s Manual

Maximum number of identical transport

packages/items which may be stacked on the
bottom package, where “6” is the limiting number.
Symbol for the marking of electrical and
electronics devices according to Directive
2002/96/EC.

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 Patient Monitor User’s Manual

Chapter 3 Basic Operations

3.1 Unpacking and Checking

Open the package. Parts are as follows in the package .Take

out the monitor and its accessories.
Parts Standard Optional Quantity
3-lead/5-lead ECG
√ 1
cable
SpO2 probes √ 1
this
User’s manual √
manual
QC certificate √ 1
Packing list √ 1
Power adapter √ 1
USB data cable √ 1
Carrying case √ 1
Suction mount √ 1

3.2 Getting Started

Before you start to make measurements, carry out the

following checks on the monitor including all connected

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 Patient Monitor User’s Manual

modules.
——Check for any mechanical damage;
——Check for any incorrect connection of all the external
cables and accessories

 Warning:
 If the monitor is mechanically damaged, or if it is not
working properly, do not use it for any monitoring
procedure on a patient. Contact your service
personnel.
 To avoid explosion hazard, do not use the monitor in
the presence of flammable anesthetics, vapors or
liquids.

3.3 Starting the Monitor

Press the button about two seconds to turn on the

monitor. The alarm indicating lamp flashes, and then goes out.
The system gives a beep and enters the main screen.

3.4 Screen Brightness Setting

，click the right of 【Brightness】

【Menu】→【System】 ，
you can set the screen brightness to a value between 1 to 5,

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 Patient Monitor User’s Manual

choose the low level brightness to save power.

Caution: If the monitor is used outdoors or the ambient

light is strong, set the screen brightness to a
higher level.

3.5 Auto-Rotate Setting

，click the right of 【Auto-rotate】

【Menu】→【System】
to select 【On】 or 【Off】. If you select 【On】, the screen
can react to the gravity. When the monitor rotates, the screen
will rotate the display direction automatically.

3.6 Date & Time Setting

After starting up, you need to set date and time of this
monitor. Operations are as follows:
1. Select 【Menu】→【System】to enter the System menu
shown as follows:
2. Select【Use 24-hour format】, it can be set to【24h】or
【12h】.
3. Select 【Date format】, it can be set to【YYYY/MM/DD】、
【MM/DD/YYYY】or【DD/MM/YYYY】.

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 Patient Monitor User’s Manual

4. Set the current date and time and select【OK】to confirm it.

3.7 Patient Information Setting

Caution: The alarm limits of different parameters

depend on the patient type. If you set patient
type incorrectly, the monitor will judge
patient condition by current setting, which
might be wrong for your patient.

Please select patient information correctly before

measuring, Click 【ID】 on the left bottom of main screen to
enter into 【Patient Info.】. You also can select 【Menu】→
【System】→【Patient Info.】. Setting shown as follow:
1. Click the right of 【ID】to set it values.
2. Set【Type】to【Adult】,【Pediatric】or【Neonate】.
3. Select 【Pace】to 【Yes】when patient with pacemaker.

3.8 Demo Mode Setting

To enter the demo mode:

Select 【Menu】→【System】→【Maintenance】→enter

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 Patient Monitor User’s Manual

the required password. Click the right of 【Demo】to turn on.

To exit the demo mode:
Select 【Menu】→【System】→【Maintenance】→enter the
required password. Click the right of 【Demo】to turn off.

Caution: The Demo mode is for demonstration purpose

only. To avoid that the simulated data are
mistaken for the monitored patient’s data, you
should not enter the Demo mode during a
patient is being monitored. Otherwise,
improper patient monitoring and delayed
treatment could result.

3.9 Language Setting

Select 【Menu】→【System】→【Maintenance】, enter the

required password. On 【Factory Mainten.】interface, you can
select 【Language】and then choose a desired language.

3.10 Checking the Version

Select【Menu】→【System】to check the version of the

monitor software.

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 Patient Monitor User’s Manual

3.11 Restoring the Factory Configuration

If you have changed the system’s configuration and want to

restore the factory configuration, follow this procedure:
1. Select【Menu】→【System】.
2. Select【Set to Default】, popping up a confirming window,
select【OK】to restore the factory configuration.

Caution: The factory configuration only can be set by

manual.

3.12 Shutting off the Monitor

Pressing power button about 2s can turn off the monitor.

1. Confirm that the patient monitoring is finished.
2. Disconnect all sensors and cables form the monitor.
3. Press the power button and hold it for 2s to turn off the
monitor. If the monitor can’t be switched off normally,
forced close the monitor by pressing and holding the power
switch more than 5s. This may cause some damages to the
device.
The device will turn off automatically if any operation or
measurement is going on. Auto power-off setting: 【Menu】→

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 Patient Monitor User’s Manual

【System】→【Maintenance】, enter the required password,

click the right of 【Auto power-off setting】, you can select
“off”, “10min”, “30min”.

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Chapter 4 Alarm
Alarm refers to a prompt that is given by the monitor for
medical personnel through visual, audible and other means when
a vital sign appears abnormal or the monitor occurs technical
problem.

 Warning:
 Setting alarm limits to extreme values that can render
the alarm system useless.
 Alarm settings are restored automatically after power
is interrupted for ≤30s, the alarm setting will lose if the
power is interrupted for＞30s.

 Note: The monitor generates all the audible and visual

alarms through speaker, alarm lamp and screen.
When the monitor powers on, the alarm lamp will
be lighted in red and yellow one time and the
speaker will give a beep voice, which indicates the
alarm system of the monitor is working normally.

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 Patient Monitor User’s Manual

4.1 Alarm Categories

By nature, the monitor’s alarms can be classified into three

categories:
1. Physiological alarms
Physiological alarms are triggered by a monitored parameter
value that violates set alarm limits or an abnormal patient
condition. Physiological alarm message are displayed in the
physiological alarm area.
2. Technical alarms
Technical alarms are triggered by a device malfunction or a
patient data distortion due to improper operation or system
problems. Technical alarm messages are displayed in the
technical alarm area.
3. Prompt messages
As a matter of fact, prompt messages are not alarm messages.
Apart from the physiological and technical alarm messages, the
pulse monitor will show some messages telling the system status.
Prompt messages are displayed in the technical alarm area.

4.2 Alarm Levels

1. By severity, the monitor’s physiological alarms can be

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 Patient Monitor User’s Manual

classified into three categories: high level alarms, medium

level alarms and low level alarms.
 High level alarms
Indicate that the patient is in a life threatening situation
and an emergency treatment is demanded.
 Medium level alarms
Indicate that the patient’s vital signs appear abnormal and
an immediate treatment may be required.
 Low level alarms
Indicate that the patent’s vital signs appear abnormal and
an immediate treatment may be required.
2. By severity, the monitor’s technical alarms can be
classified into three categories: high level, medium level
alarms and low level alarms.

Caution:
 The levels of technical alarms are predefined before
the monitor leaves the factory and cannot be changed
by users.
 The level of technical alarm can’t be changed by the
user.

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4.3 Alarm Indicators

When an alarm occurs, the monitor will raise user’s attention

by the following indications:
 Alarm tone: According to alarm level, speaker in the
monitor gives alarm sound in different tone.
 Alarm lamp: According to alarm level, alarm lamp on
monitor flashes in different color speed.
 Alarm message: Alarm message are displayed on the
screen.
 Flashing numeric: The numeric of parameter in alarm
flashes.

Caution: For different alarm levels, the alarm lamp,

alarm tone and alarm messages presented
are different.

4.3.1. Alarm Tone

The different level alarms are indicated by the system in

following different audio ways:

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 Patient Monitor User’s Manual

Alarm
Audible prompt
level

High “DO-DO-DO------DO-DO,DO-DO-DO------DO-DO”

Medium “DO-DO-DO”

Low “DO-”

4.3.2. Alarm Lamp

When an alarm occurs, the alarm levels are indicated in the

following different visual ways:

Alarm level Visual prompt

High Alarm lamp flashes in red with 2 Hz.

Medium Alarm lamp flashes in yellow with 0.5 Hz.

Alarm lamp lights on in yellow without

Low
flashing.

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 Patient Monitor User’s Manual

Caution:
 When multiple alarms of different levels occur at the
same time, the monitor will select the alarm of highest
level give visual and alarm indications.
 When multiple alarms occur at the same time, the
alarm message will be displayed in the alarm area in
turn.

4.3.3. Alarm Message

When an alarm occurs, the alarm message will be displayed

in the alarm area:
 The system uses the following symbols to match the alarm
level of physiological alarm messages:
High level alarms: ***
Medium level alarms: **
Low level alarms: *
 The system uses different background colors for the alarm
message to match the alarm level:
High level alarms: red
Medium level alarms: yellow
Low level alarms: yellow

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 Patiient Monitor User’s Manual

 Prompt messaage: blue.

4.3.4. Flashing Numeric

N

When a physiiological alarm occurs, the nu

umeric of
parameter will flash..

4.4 Alarm Sta

atus Symbol

To ideentify the control for alarm pau

used or to
indicatte that the alarm system is in the alarm
paused
d state.
Indicattes the alarm sound is turned off.
To iden
ntify the control for alarm reset.

4.5 Alarm Ton

ne Configuration

1. The minimum
m alarm volume setting.
Select 【Menu】
】→【System】→【Maintenancce】→enter
the required passworrd, select 【Machine Mainten.】→【Alarm
Setup】→【Min.Alm
m.Vol.】, you can select “0, High, Mid,
M Low”.
2. Alarm volumee setting
Select 【Menu】
】→【System】→【Alarm Volu
ume】, you
can select from X to high. Attention: “X” means: the value
v of the

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 Patiient Monitor User’s Manual

ume.
minimum alarm volu

 Warning: Auditory
A alarm signal sound pressure
levels,
l which are less than ambiient levels,
can
c impede operator recognition
n of alarm
conditions.
c

4.6 Pausing Alarms

A

Press the button

n on the front panel of mo
onitor, you
can suspend all alarm
m indicators of the monitor about 60s:
6
 The visual alarm
a and audible alarm are all susspended.
 The parameeters of physiological alarm stop fllashing.
 The alarm message
m in the physiological alarm
m area will
not be displlayed.
 The remain
ning time and the icon will bee shown in
the physiolo
ogical alarm area.
 The techniccal alarm message will still be shown in the
technical alaarm area.
 The alarm of lead-off/sensor-off turns into
o a prompt
message.
After the alarm paused time, the monitor will auttomatically
using. Press again the button
cancel the alarm pau , the alarm

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 Patient Monitor User’s Manual

pausing can be cancelled by manual operation.

4.7 Adjust the Alarm Volume to Zero

Set the 【Min.Alm.Vol.】and【Alarm Volume】to 【0】 to

adjust the alarm volume to 0. Then there will be a symbol
shown in the alarm status area. The alarm lamp and alarm
messages are still active after the alarm volume is set to 0. The
audible alarm is reactivated automatically when:
 The factory configuration is finished;
 Set the alarm volume to a nonzero value.
When a factory configuration is selected, the alarm volume
of the monitor may be lower than the minimum alarm volume.
In this case the alarm volume is automatically adjusted
according to the minimum alarm volume.

 Warning:
 Potential hazard can exist if different alarm pre-sets
are used for the same of similar equipment in any
single area.
 When the alarm sound is adjusted to 0, the monitor
will give no audible alarm tones even if a new alarm
occurs. Therefore the user should be very carefully

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 Patiient Monitor User’s Manual

about whetheer to adjust the alarm volume to 0 or not.

 Don’t rely ex
xclusively on the audible alarm system
s for
patient monitoring. Adjusting alarm volumee to a low
level may reesult in a hazard to the patien
nt. Always
keep the patieent under close surveillance.

4.8 Alarm Reset

Select 【Menu
u】→【System】→【Alarm reseet】.
Press alarm reset , you can reset the alarm system::
 It will exit alaarm pause if it is on the condition of alarm
pause.
 It only turns offf audible alarm， the visual is go
oing on for
the existing alarm.
 The audible alarm will be restored when a new
n alarm
occurs.
 The parameters of physiological alarm keep on flaashing.
 The alarm of lead-off/sensor-off turns into a prompt
message.

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4.9 When an Alarm Occurs

 Note: When an alarm occurs, you should always

check the patient’s condition first.

Check the alarm message appeared on screen. It is needed to

identify the alarm and action appropriately, according to the
cause of the alarm.
1. Check the patient’s condition.
2. Identify alarming parameter and alarm category.
3. Identify the cause of the alarm.
4. Silence the alarm, if necessary.
5. When cause of alarm has been over, check that the
alarm system is working properly.
You will find the alarm message for the individual parameter
in Appendix C Alarm message.

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 Patient Monitor User’s Manual

Chapter 5 Measuring ECG

5.1 Introduction
Before the mechanical contraction, the heart will firstly
produce electrization and biological current, which will be
conducted to body surface through tissue and humors; the current
will present difference in potential in different locations of the
body, forming potential difference ECG, also known as body
surface ECG or regular ECG, is obtained by recording this
changing potential difference to form a dynamic curve. Monitor
measures the changes in the body surface potentials caused by the
heart of the patient, observe the cardioelectric activities, record
the cardioelectric waveforms and calculate the HR through the
multiple electrodes connected to ECG cable.

5.2 Safety Information

 Warning:
 It is imperative to only use the ECG electrodes and
cables provided by manufacturer or specified in this
manual. Users shall use the electrode which has little
polarization voltage and little contact resistance.

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 Patient Monitor User’s Manual

 When conducting defibrillation, it is imperative to

only use the ECG electrodes and cables specified by
manufacturer.
 Check the ECG cable and its package for any sign of
damage before use. Do not use the cable if any damage
is detected.
 Do not come into contact with the patient during
defibrillation. Otherwise serious injury or death could
result.
 When the electrode polarized voltage is too high, the
monitor will indicate the abnormal state by alarm
system.
 When you are connecting the electrodes or the patient
cable, make sure that the connectors never come into
contact with other conductive parts, or with earth. In
particular, make sure that all of the ECG electrodes
are attached to the patient, to prevent them from
contacting conductive parts or earth.
 Please check the skin where the electrodes are placed,
replace the electrodes or relocate the electrodes in case
of skin allergy occurs.
 Interference from instruments near the patient and

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 Patient Monitor User’s Manual

ESU interference can cause problems with the ECG

wave.
 The monitor cannot be directly applied to heart and
cannot be used for the measurement of endocardio
ECG.
 Line isolation monitor transients may resemble actual
cardiac waveforms and thus inhibit heart rate alarm,
at this time, you should unplug power adapter and
supply power by lithium battery.

5.3 Monitoring Procedure

5.3.1 Skin Preparation for Electrode Placement

Good electrode-to-skin contact is important for a good ECG

signal, as the skin is a poor conductor of electricity. It is necessary
to deal with the skin properly before placing the electrodes. The
steps are shown as follows:
1. Select sites with intact skin, without impairment of any
kind.
2. Clip or shave hair from sites as necessary.

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 Patient Monitor User’s Manual

3. Gently abrade the skin to remove dead skin cells to

improve the conductivity of the electrode site.
4. Wash sites thoroughly with soap and water, leaving no
soap residue.( We do not recommend using ether or pure
alcohol, because this dries the skin and increases the
resistance.)
5. Dry skin thoroughly.

5.3.2 Placing Electrode

1. Preparation before electrode placement

1) Skin preparation (refers to Chapter 5.3.1).
2) Check if the buttons on the electrodes are clean and free of
damage.
3) Place the electrodes on the body of patient. Before
attaching, smear some conducting cream on the electrodes
if the electrodes are not electrolyte self-supplied.
4) Connect the cable leads to the electrodes through the
buttons of the electrodes.

 Note:
 For patients who tremble a lot or patients with
especially weak ECG signals, it might be difficult to

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 Patient Monitor User’s Manual

extract the ECG signals, and it is even more difficult to

conduct HR calculation. For severely burnt patients, it
may be impossible to stick the electrodes on and it may
be necessary to use the special pin-shape electrodes. In
case of bad signals, care should be taken to place the
electrodes on the soft portions of the muscle.
 Check the irritation caused by each electrode to the
skin, and in case of any inflammations or allergies, the
electrodes should be replaced and the user should
relocate the electrodes every 24 hours or at a shorter
interval.
 When the amplifier is saturated or overloaded, the
input signal is medical meaningless, then the
equipment gives an indication on the screen.

2. Electrode Placement
 3-Lead
Take the AHA standard as an example, when conducting
3-lead ECG monitoring, use 3-lead ECG cable. The three
limb-leads of RA, LA and LL as shown in below figure, will be
placed on the relevant locations. This connection can establish
the lead of I, II, III.

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 Patient Monitor User’s Manual

LA RA

LL

 5-Lead
Take the AHA standard for example, when conducting
7-lead ECG monitoring, use 5-lead ECG cable. The four
limb-leads of RA, LA, RL and LL as shown in below figure, will
be placed on the relevant locations. This connection can
establish the lead of I, II, III, aVR, aVL, aVF; according to
actual needs, chest lead V can be placed on any of the locations
between V1~V6, respectively making one lead of V1~V6
established.

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 Patient Monitor User’s Manual

RA LA

RL LL

 Warning:
 To avoid burning, when the electrotome operation is
performed, the electrodes should be placed near the
middle between ESU grounding pad and electrotome
and the electrotome should be applied as far as
possible from all other electrodes, a distance of at least
15 cm/6 in is recommended.
 When using the ESU device, avoid placing the
electrodes near the ESU grounding pad, otherwise,

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 Patiient Monitor User’s Manual

grate deal intterference will influence the EC

CG signals.
The monitor should be placed far from the operating
table. Powerr wires and the ECG cables should be
partitioned and should not be in parallel.

5.3.3 Connecting ECG Cable

Plug the ECG cable into the ECG connector. An ECG

waveform and numeeric appears on the monitor disp
play. Using
the shortcut key on the right of monitor to staart or pause
ECG measurement.

5.3.4 Selecting leeads

Depending on th
he patient to be monitored, you shall
s select
the proper leads. Enter into 【ECG Setup】to sellect【Lead
Type】.

5.4 Checking Paced Status

t set the paced status correctly when you

It is important to
start monitoring ECG
G.
If the【Pace】status has been set to【Yes】, If the system

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 Patient Monitor User’s Manual

detects paced signal, the symbol “︱” will be marked on the

ECG wave.
To change the paced status, you can review 3.7 Patient
Information Setting.

 Warning:
 For paced patients, you must set 【Paced】to【Yes】.
If it is incorrectly set to【No】, the monitor could
mistake pace pulses for regular QRS complexes and
fail to alarm during asystole.
 Some pace pulses can be difficult to reject. When this
happens, the pulses are counted as a QRS complex, and
could result in an incorrect HR and failure to detect
cardiac arrest or some arrhythmias. Keep pacemaker
patients under close observation.
 For non-paced patients, you must set【Paced】to【No】,
otherwise, the system cannot detect the arrhythmia
related to Ventricular Premature (including PVCs
count), and will not conduct ST analysis.

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 Patient Monitor User’s Manual

5.5 ECG Display

1
2
3
4
6

Fig 5-1 ECG Display

1. HR label 2.HR high alarm limit 3.HR value
4. HR low alarm limit 5. ECG waveform
6. Pacemake pulse symbol 7.Scan speed

5.6 Setting ECG

Select 【Menu】→【ECG Setup】, enter into ECG setup

interface.

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 Patiient Monitor User’s Manual

Fig
F 5-2 ECG Setup Interface

5.6.1 Setting HR
R Alarm

Click the right off 【HR Alm】, you can select “M

Mid, High”.

5.6.2 Setting HR
R Alarm Limits

Click the right of

o 【HR Uplimit】or 【HR Downllimit】, you
can set the HR uplim
mit and downlimit. Attention: The high alarm
should greater than the
t low one.

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 Patient Monitor User’s Manual

5.6.3 Setting ECG Scan Speed

Select scan speed of ECG waveform. Click the right of

【Speed】, you can select “6.25 mm/s、12.5mm/s, 25 mm/s”.

5.6.4 Setting ECG Gain

Select the gain item of ECG waveform. Click the right of

【ECG Gain】, you can select “2.5 mm/mV、5 mm/mV、10
mm/mV”.

5.6.5 Setting Lead Type

Select the lead type of ECG input.

 If the monitor only has 3 lead, you can select “3 lead” as
lead type.
 If the monitor has 3 lead and 5 lead, you can select “3 lead”
or “5 lead” as lead type.

5.6.6 Setting Primary Lead

Select the ECG waveform, and this lead is the key

monitoring lead。
 If lead type is 3 lead, you can select “I，II，III”.
 If lead type is 5 lead, you can select” I，II，III，aVR，
aVL，aVF，Vx”.

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5.6.7 Setting Lead Layout

 If lead type is 3 lead, you can select ”Primary Lead”.

 If lead type is 5 lead, you can select” Primary Lead,
7-Lead”.

5.6.8 Setting QRS Volume

Click the right of 【QRS Vol.】,you can select “Off, High,

Mid, Low”.

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Chapter 6 Measuring RESP

6.1 Principle of Measuring

Monitor measures RESP with the method of impedance.

When a patient exhales and inhales, changes will take place in
the size and shape of the thoracic cavity, causing consequent
changes in the impedance between the two electrodes installed at
the patient’s chest. Based on the cycle of impedance changes, the
respiration rate can be calculated. The measuring range of
respiration rate is from 0/minute to 150/minutes.

6.2 Preparatory Steps of Measurement

1） Plug the 5-lead ECG cable into the ECG socket of the
monitor.
2） Place the various pads of the electrodes onto the body of
patient and connect them to the relevant lead cables. At this
moment, the screen will show Resp waves and the RESP
rate will be calculated.
3） Set the parameters relevant to Resp monitoring.
To measure Resp parameters, it is unnecessary to use other
cables and it is only necessary to use the two RA and LL leads in

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 Patient Monitor User’s Manual

the 5-lead ECG cable. So please plug the 5-lead ECG cable into
the ECG socket and refer to 5.3 Monitoring Procedure to place
the RA and LL leads onto the body of patient.

 Warning: For the sake of safety, all the leads on the

5-lead ECG cable must be connected to the
body of patient.

 Caution:
 In order to get the best Resp waveforms, when
selecting leadⅡfor measuring Resp, it is advised to
place RA and LL electrodes cornerways.
 For reducing the influence of rhythmic blood flow on
Resp electrode pickup impedance changes, avoid the
liver area and ventricles of heart in the line between
RA and LL electrodes. This is particularly important
for neonates.
 The measurement of RESP is not applicable for
patient with excessive motion, otherwise it may cause
the mistake of RESP alarm.

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 Patient Monitor User’s Manual

6.3 Resp Display

1

6
3

Fig 6-1 Resp Display

1. Resp label 2.Resp waveform
3. Resp uplimit value 4. Resp value
5. Resp downlimit value 6. Resp unit

6.4 Resp Setup

Select 【Menu】→【Resp Setup】, enter into Resp setup

interface.

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 Patiient Monitor User’s Manual

Fig
F 6-2 Resp Setup Interface

6.4.1 Resp Alarm

m Setup

Click the right off【Resp Alm】, you can select “M

Mid, High”.

6.4.2 Resp Alarm

m Limits Setup
Click the right off 【Uplimit】or 【Downlimit】, you
y can set
the Resp uplimit and
d downlimit. Attention: The high alarm
a limit
should greater than the
t low one.

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 Patient Monitor User’s Manual

6.4.3 Resp Scan Speed Setup

Select scan speed of Resp waveform. Click the right of

【Speed】, you can select “6.25 mm/s,12.5mm/s, 25 mm/s”.

6.4.4 Gain Setup

Select gain of Resp waveform. Click the right of【Gain】,

you can select “x0.25 ,x1,x2”.

6.4.5 Resp Lead Setup

Select computing method of Resp lead. Click the right of

【Resp Lead】, you can select “RA-LA，RA-LL”.

6.4.6 Apnea Alarm Setup

Suffocation alarm occurs when the time of zero Resp rate

has reached this time scale. Click the right of 【Apnea Alarm】,
you can select “Off, 5s, 10s, 20s, 40s, 60s, 80s, 100s, 120s”.

6.4.7 Resp Anti-Drift Setup

Click the right of 【Resp Anti-Drift】, you can turn on or

turn off this function.

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Chapter 7 Measuring SpO2

7.1 Introduction
The measurement of oxygen saturation of arterial blood
(also known as pulse oxygen saturation, usually shortened as
SpO2) adopts the principles of light spectra and volume tracing.
The LED emits lights with two specific wavelengths, which are
selectively absorbed by oxygenated hemoglobin and
deoxyhemoglobin. The optical receptor measures the changes in
the light intensity after the light passes the capillary network and
estimates the ratio of oxygenated hemoglobin and the total
hemoglobin.
oxygenated hemoglobin
SpO2 % = x 100%
oxyhemoglobin + deoxyhemoglobin

Wavelengths of the light emitted by the pulse oximeter

probe are nominally 660nm for red LED and 940nm for infrared
LED.

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7.2 Safety Information

 Warning :
 Use only SpO2 sensors specified in this manual. Follow
the SpO2 sensor’s instructions for use and adhere to
all warnings and cautions.
 When a trend toward patient deoxygenation is
indicated, blood samples should be analyzed by a
laboratory co-oximeter to completely understand the
patient’s conditions.
 Do not use the monitor and the SpO2 sensor during
magnetic resonance imaging (MRI). Induced current
could cause burns.
 Prolonged continuous monitoring may increase the
risk of unexpected changes in skin characteristics,
such as irritation, reddening, blistering or burns.
Inspect the sensor site every two hours and move the
sensor if the skin quality changes. For neonates, or
patients with poor peripheral blood circulation or
sensitive skin, inspect the sensor site more frequently.
 Measurements and pulse signals can be affected by
certain environmental conditions, sensor application
errors, and certain patient conditions. See the
appropriate sections of this manual for specific safety

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 Patient Monitor User’s Manual

information.
 Check the SpO2 sensor and its package for any sign of
damage before use. Do not use the sensor if any
damage is detected.
 When disposing the disposable SpO2 probe or useless
SpO2 probe, please observe all local, state, and federal
regulations that relate to the disposal of this products
or similar products.

Caution: In case it is necessary to add a clip to fix the

fingertip sensor, the cable instead of the
sensor itself should be clipped. Please note
that the cable of sensor should not be pulled
with force.

 Note:
 The pleth wave is not equal to the intensity of PR
signal.
 The monitor does not provide automatic
self-examination alarm signal and the operator has to
use SpO2 simulator for self-examination.
 A functional tester cannot be used to assess the
accuracy of SpO2 of the monitor.

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 Patient Monitor User’s Manual

7.3 Monitoring Procedure

1. Selecting SpO2 Sensor

Depending on the patient category, weight and application
site, you can select the SpO2 sensor as required.
2. Connecting SpO2 Sensor
Plug the SpO2 sensor cable into the SpO2 connector on the
measurement module.
3. Applying SpO2 Sensor
Clean the application site, such as colored nail polish, and
apply the sensor to the finger of patient.

 Warning:
 Do not use the SpO2 sensor on a limb where the NIBP
cuff is applied. This may result in inaccurate SpO2
reading due to blocked blood flow during cuff
inflation.
 Do not conduct SpO2 measurement on the finger
smeared with nail polish, otherwise unreliable
measurement results might be produced.
 When using finger sensor, make sure the nail faces to
the light window.

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7.4 SpO2 Display

 Parameter Display

1 5

Fig 7-1 SpO2 Parameter

1. SpO2 label 2. High alarm limit of SpO2

3. Low alarm limit of SpO2 4. SpO2 value

5. SpO2 unit

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 Patient Monitor User’s Manual

 Waveform Display

Fig 7-2 SpO2 Volume Curve

7.5 PR Display

1 5

Fig 7-3 PR Display

1. PR label 2. High alarm limit of PR
3. Low alarm limit of PR 4. PR value 5. PR unit

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 Patiient Monitor User’s Manual

Caution: Duriing the monitoring of HR and PR,

displaying of HR has priority. That is PR will
be displayed
d only when there isn’t HR
moniitoring.

7.6 SpO2 Setu

up
Select 【Menu】
】→【SpO2 Setup】, enter into SpO2
S Setup
interface.

Fig 7-4 SpO2 Setup

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 Patient Monitor User’s Manual

7.6.1 SpO2 Alarm Setup

Click the right of 【Alarm】, you can set alarm level of SpO2
and PR, you can select “Mid, High”

7.6.2 SpO2 Alarm Limits Setup

Click the right of 【Uplimit】or 【Downlimit】, you can set

the SpO2 and PR uplimit and downlimit. Attention: The high
alarm limit should greater than the low one. The downlimit for
SpO2 should be higher than Desat limit.

7.6.3 Scan Speed Setup

Click the right of 【Speed】, you can select “6.25 mm/s、
12.5mm/s, 25 mm/s”.

7.6.4 Average Time Setup

Select the average time for SpO2. The shorter the averaging
time is, the quicker the monitor responds to the change in the
patient’s oxygen saturation level. Click the right of【Avg Time】,
you can select “4s, 8s, 16s”.

7.6.5 QRS Volume Setup

Click the right of【QRS Vol.】, you can select “Off, High,

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 Patient Monitor User’s Manual

Mid, Low”.

7.7 Desat limit Setup

SpO2 desat means when SpO2 measuring value is lower than
the desat limit, a high physiological alarm will be trigged. Its
setting is as follows.
1、 Select【Menu】→【System】→【Maintenance】, enter the
required password.
2、 Select【Machine Mainten】→【SpO2 Setup】→【Desat
limit】, click the right of 【Desat limit】to set its value.

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 Patiient Monitor User’s Manual

Chapter 8 Trrend Review

8.1 Introductiion

Select 【Menu】→【Trend】to enter trend reviewing

window. In the wind
dow, you can review ECG, Reap,, SpO2 and
PR data stored beforre.

8.2 Review In
nterface

Fig 8-1 Review Interface

If the trend date is not only one page, you can turn pages

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 Patiient Monitor User’s Manual

xt】or【Pre.】.
by clicking the【nex

8.3 Review Seetup

Click the right of 【ID】to select patient’s ID

D, you can
review patient’s trend review by selecting different ID.

Fig
g 8-2 ID Review Interface
Click the right off 【More】on the top of review intterface, the
drop-down window shown
s as following:

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 Patiient Monitor User’s Manual

Fig 8-3 The

T drop-down Window of “Morre”
You can set 【S
Save time】, 【Delete】, 【Deelete all】,
n this interface.
【Transmission】in
 Save time: To
o adjust recording time, you can select1“0s,
30s, 1min, 2 min,
m 5min, 10min”.
 Delete: To dellete trend data of the selected ID No.
N
 Delete all: To delete trend data of all patients.
 n: To send trend. Before the operation,
Transmission
“review systtem of monitoring data” pro
ovided by
manufacturer must be opened, and connect com
mputer and
monitor with the USB connector. After sendiing all the
u can check them in the computer..
trend data, you

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Chapter 9 Battery

9.1 Introductiion

A rechargeable and
a maintenance-free battery is deesigned for
Patient Monitor, wh
hich enables continuous working when AC
power off.

 Warning：Thee replacement and maintenance of battery

sha
all only be conducted by the man
nufacturer.
Pleease contact to the manufacturer or its
rep
presentatives.

When a lithium ion

i battery is used, the battery ico
on indicates
the battery status as follows:
f
1. Indicates that
t the power of the battery is full；
2. Indicates that
t the power of the battery is 3 grids
g left；
3. Indicates that
t the power of the battery is 2 grids
g left；
4. Indicates that
t the power of the battery is 1 grid
g left；
5. Indicates that
t the battery is almost depleted..
Battery power supply
s can only last for a period of time. If

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 Patient Monitor User’s Manual

the voltage of batteries is too low, an alarm of “Battery Low”

will be triggered. Please insert the monitor to battery charger to
charge the battery. The monitor will be switched off
automatically 10 minutes after the first “Battery Low” alarm is
given.

9.2 Charging the Battery

To charge the battery:

1. Connect the Micro USB in power adapter,
2. Connect the other connector of Micro USB in the monitor,
and plug the adapter into the AC mains,
3. The indicating lamp on the monitor is on to indicate that
the battery is in charge,
4. When the battery charging indicating lamp on the monitor
turns off, the battery is fully charged.

9.3 Optimizing Battery Performance

A battery needs at least two optimizing cycles when it is put

into use for the first time. A battery cycle is one complete,
uninterrupted charge of the battery, followed by a complete,
uninterrupted discharge of the battery. A battery should be

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 Patient Monitor User’s Manual

conditioned regularly to maintain its useful life. Condition a

battery once when it is used or stored for two months, or when
its run time becomes noticeably shorter.
To optimize a battery, follow this procedure:
1. Disconnect the monitor from the patient and stop all
monitoring and measuring procedures.
2. Place the monitor in the charger stand and connect the AC
mains. Allow the battery to be charged uninterruptedly for
above 4 hours.
3. Remove the AC mains and allow the monitor to run from
the battery until it shuts off.
4. Replace the monitor in the charger stand and connect the
AC mains. Allow the battery to be charged uninterruptedly
for above 4 hours.
5. The optimizing of the battery is over.

9.4 Checking the Lithium Battery

The performance of a battery may deteriorate over time. To

check the performance of a battery, follow this procedure:
1. Disconnect the monitor from the patient and stop all
monitoring and measuring procedures.
2. Place the monitor in the charger stand and connect the AC

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 Patient Monitor User’s Manual

mains. Allow the battery to be charged uninterruptedly for

above 4 hours.
3. Disconnect AC mains and allow the monitor to run on the
battery until it shuts off.
4. The operating time of a battery reflects its performance
directly.

9.5 Disposing of the Batteries

Batteries that are damaged or depleted should be replaced

and discarded properly. Dispose of used batteries according to
local regulations.

 Warning: Do not disassemble batteries, or dispose of

them in fire, or cause them to short circuit.
They may ignite, explode, or leak, causing
personal injury.

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Chapter 10 Maintenance and Cleaning

10.1 Introduction

Keep your equipment and accessories free of dust and dirt.

To avoid damage to the equipment, follow these rules:
1. Always dilute according the manufacturer’s instructions
or use lowest possible concentration.
2. Do not immerse part of the equipment in the liquid.
3. Do not pour liquid onto the equipment or accessories.
4. Do not allow liquid to enter the case.
5. Never use abrasive materials (such as steel wool or silver
polish), or erosive cleaners (such as acetone or
acetone-based cleaners).

 Warning:
 Be sure to shut down the system and disconnect all
power cables from the outlets before cleaning the
equipment.
 For optimal performance, product service should be
performed only by qualified service personnel

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Caution: If you spill liquid into the equipment of

accessories, connect you service personal or
us.

10.2 Seasonal Safety Checking

 Note: To ensure the performance and safety of

equipment, it must be checked after using 1
year. When check the equipment, please
contact professional technology engineers.

Please clean the plug of power cord at least once a year. Too
much dust on plug may cause the fire.
The following safety checks should be performed at least
every 12 months by a qualified person who has adequate training,
knowledge, and practical experience to perform these tests.
The data should be recorded in an equipment log. If the
device is not functioning properly or fails any of the following
tests, the device has to be repaired.
① Inspect the equipment and accessories for mechanical and

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 Patient Monitor User’s Manual

functional damage.
② Inspect the safety relevant labels for legibility.
③ Verify that the device functions properly as described in the
instructions for use.
④ Test the earth leakage current according IEC 60601-1 Limit:
NC 500μA, SFC: 1000μA.
⑤ Test the enclosure leakage current according to IEC 60601-1:
Limit: NC 100μA, SFC: 500μA.
⑥ Test the patient leakage current (normal operation) according
IEC 60601-1
Limit: type CF: for a.c.: 10μA, for d.c.: 10μA.
⑦ Test the patient leakage current under single fault condition
according IEC 60601-1
Limit: type CF: for a.c.: 50μA, for d.c.: 50μA.
⑧ Test the patient leakage current Mains voltage on applied part:
According IEC 60601-1:
Limit: type CF: for a.c.: 50uA.

 Warning: No use-serviceable parts inside, before

servicing to authorized representative or
manufacturer.

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10.3 Cleaning the Monitor

1. Common detergent and non-corrosive disinfectant used in

hospital can be applied to clean monitor, however you must
be aware that many kinds of detergents must be diluted prior
to utilization, and please use it according to the instruction of
detergent manufacturer.
2. Avoid the use of alcohols, amino or acetonyl detergent.
3. The enclosure and screen of monitor shall be free of dust, and
they can be wiped with lint-free soft cloth or sponge soaked
in detergent. While cleaning, be careful and do not spill
liquid onto the instrument and keep any liquid out of it. When
wiping the side panel of monitor, you must be especially
careful to keep water out of all kinds of cable and outlet on
the panel.
4. Do not use abrasive material including wire brush or metal
brightener during cleaning because this material will damage
the panel and monitor screen.
5. Do not submerge the monitor in liquid.
6. While cable or plug of attachment accidentally gets wet,
please rinse it with distilled water or deionized water and
dry it in the environment of temperature 40℃ to 80℃ for at
least one hour.

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 Patient Monitor User’s Manual

10.4 Cleaning ECG Cable

The recommended disinfectors include glutaric dialdehyde

solution and 10% decolourant solution.
a) Please clean cable prior to sterilization.
b) Clean the cable surface with soft cloth bedewed with some
fresh water or neutral soapy water.
c) Scrub cable with soft cloth bedewed with some disinfector.
d) Wipe off the disinfector remaining on cable by soft cloth
bedewed with fresh water.
e) Put cable in a shady and cool environment for airing.
Attention:
 Do not sterilize lead wire with high-pressure, radioactive
or steam device.
 Do not directly submerge lead wire in liquid.
 To avoid long-time harm to cable, it is suggested that
sterilization to the product be conducted only when
necessary according to the regulation of your hospital.
 Do not clean and reuse disposable electrode.

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 Patient Monitor User’s Manual

10.5 Cleaning SpO2 Sensor

1. The casing of the sensor and light tube can be cleaned with
swab or non-velvet soft cloth dipped with medical alcohol.
2. The sensor cable can be cleaned or sterilized with Hydrogen
Peroxide 3% or isopropyl alcohol 70%.
3. It is forbidden to put the monitor in high-pressure containers
and put the sensor directly in liquid.

 Warning: Do not reuse or disinfect the disposable SpO2

sensor.

10.6 Disposal

Dispose of the monitor in accordance with local

environment and waste disposal laws and regulations. For the
disposal of SpO2 sensor and ECG cable, follow local regulations
regarding disposal of hospital waste.

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 Patient Monitor User’s Manual

Chapter 11 Accessories

 Warning:
 Use only accessories specified in this manual. Using
other accessories may cause damage to the monitor.
 Disposable accessories are designed for single-patient
use only. Reuse of them may cause a risk of
contamination and affect the measurement accuracy.
 Check the accessories and their packages for any sign
of damage. Do not use them if any damage is
detected.

Type Model PN

Adult 15-100-0008
ECG Electrode
Pediatric/Neonatal 15-100-0009

3 lead, IEC 15-048-0002

ECG Cable
3 lead, AHA 15-048-0001

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 Patient Monitor User’s Manual

Type Model PN

5 lead, IEC 15-048-0004

ECG Cable
5 lead, AHA 15-048-0003

usable，adult 15-100-0013

SpO2 sensor usable，pediatric 15-100-0014

usable，neonatal 15-100-0015

Power adapter LXCP12-005 15-048-0020

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 Patient Monitor User’s Manual

Appendix A Product Specifications

A.1 Safety Specifications

Class IIb (Rule 10 of Annex

Classification
IX of the MDD 93/42/EEC)
Type of protection against electric II with internal power or
shock external power device
Type CF applied part,
Degree of protection against
defibrillation protected
electric shock
（ECG, SpO2）
Ordinary equipment, without
Degree of protection against
protection against hazards of
hazards of explosion
explosion
Degree of protection against
IPX1
ingress of liquid
Equipment type Portable
Mode of operation Continuous
EMC Group 1, class A

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 Patient Monitor User’s Manual

A.2 Physical Specifications

350g(full configuration, including the

Mainframe weight
batteries)
Mainframe size 142mm(W)×78mm(H)×36mm(D)

A.3 Environmental Specifications

Operating: 5℃ to +40℃；
Temperature
Storage: -20℃ to +55℃；
Atmospheric Operating: 860hPa to 1060hPa；
pressure Storage: 500hPa to 1060hPa；
Operating: 15% to 85%(non condensing)
Humidity
Storage: less than 93%(non condensing)

A.4 Charging Specifications

A4.1 Power Adapter

Micro USB Charge, Data export

Power adapter Input: AC 100～240Ｖ
Output: DC 5V/2A

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 Patient Monitor User’s Manual

A4.2 Battery Requirement

Type Built-in lithium battery

Voltage 3.7V
capacity 4800mAH
Charging time 3 hours to 90%
4 hours to 100%
Run time >28h

A.5 Hardware Specifications

A.5.1 Display

Size 4.3inch
Resolution 480*272
Touch Resistive touch
Autorotation four direction
Direction

A.5.2 Indicating Lamp

Alarm indicating 1(Yellow/Red), on the top of screen.

Battery charging 1（orange）
indicating lamp When charged, it lights orange.
When fully charged or not charged, it
doesn’t light.

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 Patient Monitor User’s Manual

A.5.3 Audio Indicating

Speaker Gives audible alarm, button tone and

QRS tone;
Supports Pitch Tone and multi-level
volume;
Alarm tones meet the requirement of IEC
60601-1-8.
Alarm pressure 45 dB to 85 dB, Testing place is 1 meter
from the tone.

A.5.4 Buttons

Power button Turn on/off

Freeze/Unfreeze ECG waveform.
Shortcut key Short press to achieve the above
function，long press + power button to
achieve calibration of LCD.

A.6 Data Storage

The changing trends of physiological parameters will be

shown in the monitor, you can select optionally PC software, to
upload trend review to computer by USB.

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 Patient Monitor User’s Manual

Patient ID 1～96

Display way Trend tabular

trend interval 10s, 30s, 1min, 2min, 5min, 10min

Storage Save when power down
500 groups/patient can be stored (only
Capacity
data, no waveform).

A.7 Measurement Specifications

A.7.1 ECG Specifications

ECG
Lead type 3-lead：I,II,III
5-lead：I, II, III, aVR, aVL, aVF, Vx
ECG input ±6mV
rang
Gain 2.5mm/mV, 5mm/mV, 10mm/mV
Input ≥5.0MΩ
impedance
Leakage ＜10 uA
Current
GMRR ≥89dB

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 Patient Monitor User’s Manual

Frequency 0.5－40Hz
response
Electrode
offset ±500mV d.c.
potential

Standardizing 1mV ±5%

signal
Protection Electric isolation voltage is 4000V at 50/60Hz
60s.
Defibrillator-proof.
Electrode off with(except RL)
indicating

Scan speed 6.25 mm/s,12.5 mm/s, 25 mm/s

Protection
against the
effects of
defibrillation
<5s after Defibrillation.
and blocking
after
defibrillation

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 Patient Monitor User’s Manual

Recovery time
of equipment
from
ECG waveform will recover to the baseline in
electrodes
10 s.
polarization
after
defibrillation
Pacemaker With pacemaker detection ， meet the
pulse symbol requirement of IEC60601-2-27: 2011
201.12.101.12 ， the pace pulse meet the
following requirements ,the pace symbol
(≥2mm) will be shown on screen：
Pulse amplitude：±2mV~±700mV
Pulse width：0.1~2.0ms
Rise time：10~100us

Electrosurgery Cut power :300W

protection Coagulation power :100W
( electrotome Change of heart rate : ≤10％
protection ) Recover time : ≤10s
Comply with the requirement of clause
4.2.9.14 in ANSI/AAMI EC 13:2002

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 Patient Monitor User’s Manual

Tall T-Wave Minimum recommended 1.2 mV T-Wave

rejection amplitude. Comply with requirement of clause
capability 4.1.2 c in ANSI/AAMI EC 13:2002.)
Heart rate ≤ 50 bpm, once every two beats;
averaging 50 bpm to 120 bpm, once every four beats;
> 120 bpm, once every six beats.
Heart rate Ventricular bigeminy : 80bpm
meter Slow alternating ventricular bigeminy : 60bpm
accuracy and Rapid alternating ventricular bigeminy :
response to 120bpm
irregular Bidirectional systoles : 90bpm
rhythm
Response time HR changes from 80bpm to 120bpm: less than
of HR meter 6s to 10s.
to change in HR changes from 80bpm to 40bpm: less
HR than 6s to 10s.
Time to alarm Vent Tachycardia 1mVp-p, 206bpm:
for Gain 0.5, Range 6.5 to 8.4 seconds, Average
Tachycardia 7.2 seconds
Gain 1.0 Range 6.1 to 6.9 seconds, Average
6.5 seconds.

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 Patient Monitor User’s Manual

HR
Measurement Adult: 15 bpm to 300 bpm
range Pediatric and Neonatal: 15 bpm to 350 bpm
1 bpm
Resolution

±1% or ±1 bpm, whichever is greater

Accuracy

Detecting ≥0.20mVpp
sensitivity (II
lead)
Response time <12s
of HR meter
to change in
HR
Response of
HR to QRS Adult: without response
amplitude is
1mVp-p,
width is 10ms
0 bpm to 300 bpm, high/low limit can be
Alarm range
adjusted continuously.

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 Patient Monitor User’s Manual

A.7.2 RESP Specifications

RESP

Method Impedance

Measuring lead Lead I(RA-LA)、

II(RA-LL)optional， II(default)

Excitation frequency 64.8 kHz sine wave

Excitation voltage ≤[email protected] kHz

Measuring impedance 0.2 ~3Ω

range

Base line impedance 500~2000Ω(using defibrillation

range cable with 1Ω)

Gain X0.25、X1、X2

Resp bandwidth(BW) 0.25~2.0Hz(-3dB)

Measurement range 0~150 rpm

The high/low limit can be

adjusted continuously

Resolution 1 rpm

Accuracy ±2 rpm or ±2%

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 Patient Monitor User’s Manual

A.7.3 BLT-SpO2

SpO2
Measurement 0~100%
range
Resolution 1%
70~100%：± 2%
Accuracy
0~69%:unspecified
Alarm Select the high and low alarm limit of
SpO2
Sensor Pulse oximetry sensors contain LEDs
that emit red light at a wavelength of
approximately 660 nm and infrared light
at a wavelength of approximately 905
nm.
The total optical output power of the
sensor LEDs is less than 15 mW.
This information may be useful to
clinicians, such as those performing
photodynamic therapy.
Data update 13s
period

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 Patient Monitor User’s Manual

Anti-interference Anti-motion interference

Anti-electrotome interference
Recovery time of
equipment after 5s
defibrillation
Resisting low With powerful ability of resisting low
perfusion ability perfusion, PR amplitude can reach to
0.2% with value of SpO2 displaying.
Pitch Tone with
PR
Measurement 25 bpm ~250 bpm
range
resolution 1 bpm
accuracy ±1% or ± 1 bpm, whichever is greater
Alarm Select the high and low alarm limit of PR

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Appendix B Factory Defaults

This section lists the most important factory default settings.
These settings can be adjusted and you can load the factory
defaults if you need.

B.1 Alarm Setup

Alarm Setup Factory Default

Alarm volume Medium
Minimum alarm
Low
volume
SpO2 Alarm Level Medium
HR Alarm Level Medium
RESP Alarm Level Medium

B.2 System Setup

System setup Factory Default

QRS volume medium
Brightness 3
Scan speed 12.5mm/s

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 Patient Monitor User’s Manual

B.3 ECG Setup

HR setup Adult Pediatric Neonate

HR High Limit 120 bpm 160 bpm 200 bpm
HR Low Limit 50 bpm 75 bpm 90 bpm
RESP Adult Pediatric Neonate
Resp High Limit 30 rpm 30 rpm 100 rpm
Resp Low Limit 8 rpm 8 rpm 30 rpm

B.4 SpO2 Setup

SpO2 Setup Adult Pediatric Neonate

SpO2 High Limit 100 % 100 % 95 %
SpO2 Low Limit 90 % 90 % 85 %
PR Setup Adult Pediatric Neonate
PR High Limit 120 bpm 160 bpm 200 bpm
PR Low Limit 50 bpm 75 bpm 90 bpm

B.5 Trend Setup

Trend Setup Factory Default

Interval 30s

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 Patient Monitor User’s Manual

Appendix C Alarm Message

This section lists some important alarm message. In the
tables below, “*” means the alarm level is user-adjustable.

C.1 Physiological Alarm

SpO2 Cause Level

Alarm Messages
SpO2 Too High * High、
Medium
SpO2 Too Low * A measurement has risen High、
above the high alarm limit Medium
PR Too High * or fallen below the low High、
alarm limit Medium
PR Too Low * High、
Medium
SpO2 Desat SpO2 measurement has High
fallen below the SpO2 desat
limit.
No Pulse The pulse signal was too High
weak to be analyzed.

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 Patient Monitor User’s Manual

ECG Cause Level

Alarm Messages
HR Too High * A measurement has risen High、
above the high alarm limit Medium
HR Too Low * or fallen below the low High、
alarm limit Medium
Asystole No QRS is detected for 4 High
consecutive seconds.
RESP Too High A measurement has risen High、
above the high alarm limit Medium
RESP Too Low or fallen below the low High、
alarm limit Medium
Apnea Resp can’t be detected on High
preset-time

C.2 Technical Alarm

Message Cause Level

SpO2 Sensor Off The SpO2 sensor detached
Low
the patient or the monitor.
ECG Sensor Off The ECG sensor detached Low

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 Patient Monitor User’s Manual

the patient or the monitor.

Communication Communication error or test
Low
Error model error.
Battery Low The battery power is low Medium
SpO2 Low Perf The signal detected is weak Medium
I Polarized ECG electrode polarized Low
II Polarized ECG electrode polarized Low
V Polarized ECG electrode polarized Low

C.3 Prompt Message

Message Cause Level

searching Searching pulse Prompt
Message
SpO2 sensor SpO2 sensor disconnected Prompt
off from the patient or the monitor Message
after starting monitor, pausing
alarm or alarm reset.
ECG sensor ECG sensor disconnected Prompt
off from the patient or the monitor Message
after starting monitor, pausing
alarm or alarm reset.

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 Patient Monitor User’s Manual

Appendix D Guidance and

Manufacturer’s Declaration of EMC
Guidance and manufacturer’s declaration –
electromagnetic emissions-
for all EQUIPMENT and SYSTEMS
Guidance and manufacture’s declaration – electromagnetic emission
The monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of the monitor should assure
that it is used in such and environment.
Emission test Compliance Electromagnetic environment –
guidance
RF emissions The monitor uses RF energy only for
CISPR 11 its internal function. Therefore, its RF
Group 1 emissions are very low and are not
likely to cause any interference in
nearby electronic equipment.
RF emission The monitor is suitable for use in all
Class A
CISPR 11 establishments other than domestic
Harmonic and those directly connected to the
emissions Class A public low-voltage power supply
IEC 61000-3-2 network that supplies building used
Voltage for domestic purposes.
fluctuations/
flicker Complies
emissions
IEC 61000-3-3

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 Patient Monitor User’s Manual

Guidance and manufacturer’s declaration –

electromagnetic immunity –
for all EQUIPMENT and SYSTEMS
Guidance and manufacture’s declaration – electromagnetic
immunity
The monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of monitor should
assure that it is used in such an environment.
Electromagnetic
Immunity IEC 60601 Compliance
environment -
test test level level
guidance
Electrostatic 6 kV 6 kV Floors should be
discharge contact contact wood, concrete or
(ESD) 8 kV air 8 kV air ceramic tile. If
IEC floor are covered
61000-4-2 with synthetic
material, the
relative humidity
should be at least
30%.
Users must
eliminate static in
their hands before
use it.
Electrical fast 2 kV for 2kV for Mains power
transient/burst power power quality should be
IEC supply lines supply lines that of a typical
61000-4-4 1 kV for 1 kV for commercial or
input/output input/output hospital
lines lines environment.

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 Patient Monitor User’s Manual

Make sure there is

not impulse
interference >1kV
in use
environment.
Surge 1 kV 1 kV Mains power
IEC differential differential quality should be
61000-4-5 mode mode that of a typical
2 kV 2 kV commercial or
common common hospital
mode mode environment.
Voltage dips, <5% UT <5% UT Mains power
short (>95% dip (>95% dip quality should be
interruptions in UT) in UT) that of a typical
and voltage for 0.5 for 0.5 cycle commercial or
variations on cycle 40% UT hospital
power supply 40% UT (60% dip in environment. If the
input lines (60% dip in UT) user of the monitor
IEC UT) for 5 cycles requires continued
61000-4-11 for 5 cycles 70% UT operation during
70% UT (30% dip in power mains
(30% dip in UT) interruptions, it is
UT) for 25 recommended that
for 25 cycles the monitor be
cycles <5% UT powered from an
<5% UT (>95% dip uninterruptible
(>95% dip in UT) power supply or a
in UT) for 5 sec battery.
for 5 sec
Power 3A/m 3A/m If image distortion
frequency occurs, it may be

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 Patient Monitor User’s Manual

(50Hz) necessary to
magnetic position the
field monitor further
IEC from sources of
61000-4-8 power frequency
magnetic fields or
to install magnetic
shielding. The
power frequency
magnetic field
should be
measured in the
intended
installation
location to assure
that it is
sufficiently low.
NOTE UT is the a.c. mains voltage prior to application of the test
level.

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 Patient Monitor User’s Manual

Guidance and manufacturer’s declaration –

electromagnetic immunity –
for EQUIPMENT and SYSTEMS that are not
LIFE-SUPPORTING
Guidance and manufacture’s declaration – electromagnetic immunity
The monitor is intended for use in the electromagnetic environment
specified below. The customer or the user of monitor should assure that it is
used in such an environment.
IEC
Immunity Compliance Electromagnetic
60601 test
test level environment - guidance
level
Portable and mobile RF
communications
equipment should be used
no closer to any part of
the monitor including
cables, than the
recommended separation
distance calculated from
the equation applicable to
the frequency of the
transmitter.
Recommended
Conducted separation distance
RF 3 Vrms
 3 .5 
IEC 150 kHz to 3 V d   P
61000-4-6 80 MHz  V1 

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 Patient Monitor User’s Manual

 3.5 
Radiated RF 3 V/m 3 V/m d   P
IEC 80 MHz to  E1 
61000-4-3 2.5 GHz 80 MHz to 800 MHz

7
d  P
 E1 
800 MHz to 2.5 GHz
Where P is the maximum
output power rating of the
transmitter in watts (W)
according to the
transmitter manufacturer
and d is the recommended
separation distance in
metres (m).
Field strengths from fixed
RF transmitters, as
determined by an
electromagnetic site
survey,a should be less
than the compliance level
in each frequency range.b
Interference may occur in
the vicinity of equipment
marked with the
following symbol:

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 Patient Monitor User’s Manual

NOTE 1 At 80 MHz and 800 MHz, the higher frequency range

applies.
NOTE 2 These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.
a
Field strengths from fixed transmitters, such as base stations for radio
(cellular/cordless) telephones and land mobile radios, amateur radio, AM
and FM radio broadcast and TV broadcast cannot be predicted theoretically
with accuracy. To assess the electromagnetic environment due to fixed RF
transmitters, an electromagnetic site survey should be considered. If the
measured field strength in the location in which the monitor is used exceeds
the applicable RF compliance level above, the monitor should be observed
to verify normal operation. If abnormal performance is observed, additional
measures may be necessary, such as reorienting or relocating the monitor
b
Over the frequency range 150 kHz to 80 MHz, field strengths should
be less than 3 V/m.

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 Patient Monitor User’s Manual

Recommended separation distances between portable

and mobile RF communications equipment and
the EQUIPMENT or SYSTEM –
for EQUIPMENT or SYSTEM that are not
LIFE-SUPPORTING

Recommended separation distances between

portable and mobile RF communications equipment and the monitor
The monitor is intended for use in an electromagnetic environment in which
radiated RF disturbances are controlled. The customer or the user of the
monitor can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications
equipment (transmitters) and the monitor as recommended below, according
to the maximum output power of the communications equipment.
Separation distance according to frequency of
Rated transmitter
maximum (m)
output power of 150 kHz to 80 80 MHz to 800 800 MHz to
transmitter MHz MHz 2.5 GHz
(W)  3.5   3 .5  7
d   P d   P d  P
 V1   E1   E1 
0.01 0.12 0.12 0.23

0.1 0.37 0.37 0.74

1 1.17 1.17 2.33

10 3.69 3.69 7.38

100 11.67 11.67 23.33

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 Patient Monitor User’s Manual

For transmitters rated at a maximum output power not listed above, the
recommended separation distance d in metres (m) can be estimated using the
equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to
the transmitter manufacturer.

NOTE 1 At 80 MHz and 800 MHz, the separation distance for the higher
frequency range applies.
NOTE 2 These guidelines may not apply in all situations.
Electromagnetic propagation is affected by absorption and reflection from
structures, objects and people.

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 Patient Monitor User’s Manual

Appendix E Warranty Registration

Card
Thank you for purchasing products of BLT!
Please complete this card and mail back to BLT Service
Center in ZHUHAI within one week. If you need any
support or the defects occur, please feel free to contact us by
telephone or fax. Warranty will apply with no charge in the
warranty period (exclude accident, misuse, abuse or
misapplication). You are also and always welcome to our
service center, when you need any special service after
warranty. Do not repair the product by any person who is not
authorized or trained by BLT.

Product Model
Serial No. Contract
Date Installed Warranty
Name
Address
Contact Tele/fax
Person

27
Product name: Patient Monitor
Product type: M850
Manufacturer: Guangdong Biolight Meditech Co., Ltd.
Address: No.2 Innovation First Road, Technical Innovation
Coast, Hi-tech Zone, Zhuhai, P.R. China
Postcode: 519085

PN: 22-067-0007