Product Information
• Product Model: LifeVet CP
• Product Name: Capnograph and Pulse Oximeter
• Manufacturer: EICKEMEYER KG
• After-service Contact Information:
Address: Eltastraße 8, 78532 Tuttlingen, Germany
Phone: +49 7461 96 580 0
Fax: +49 7461 96 580 90
Email: info@eickemeyer.de
Revision History
This manual has a revision number. This revision
number changes whenever the manual is updated due to
software or technical specification change. Contents of this
manual are subject to change without prior notice.
• Revision number: V1.0
• Release time: Oct. 2016
II
Statement
Manufacturer holds the copyright of this manual, and we
are also entitled to deal with this manual as confidential files.
This manual is only used for operation, maintenance and
service of product, someone else can not publish the manual.
This manual contains exclusive information protected by
copyright laws and we reserve its copyright. Without written
approval of manufacturer no parts of this manual shall be
photocopied, xeroxed or translated into other languages.
The contents contained in this manual are subject to
amendments without notification.
Manufacturer's Responsibility
Only under the following circumstances will
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 conforms to the product
specification.
• The instrument is used in accordance with the user’s
manual.
3
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.
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.
4
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.
Contents
Chapter 1 General Introduction ......................................... 1-1
Intended Use ........................................................... 1-1
Main Unit ................................................................ 1-1
Display Views ......................................................... 1-6
Chapter 2 Safety .................................................................. 2-1
Safety Information .................................................. 2-1
Explanation of Symbols .......................................... 2-5
Chapter 3 Basic Operations ................................................ 3-1
Unpacking and Checking ........................................ 3-1
Getting Started ........................................................ 3-1
Starting the Monitor ................................................ 3-2
Screen Brightness Setting ........................................ 3-3
Auto-Rotate Setting ................................................ 3-3
Date & Time Setting ............................................... 3-3
Patient Information Setting ...................................... 3-4
Demo Mode Setting ................................................ 3-5
Language Setting .................................................... 3-5
Checking the Version .............................................. 3-6
Restoring the Factory Configuration ........................ 3-6
Shutting off the Monitor .......................................... 3-6
Chapter 4 Alarm .................................................................. 4-1
Alarm Categories .................................................... 4-1
Alarm Levels ........................................................... 4-2
Alarm Indicators ..................................................... 4-3
Alarm Status Symbol .............................................. 4-6
Alarm Tone Configuration ....................................... 4-6
Pausing Alarms ....................................................... 4-7
Shutting off the Alarm Volume ................................ 4-8
Alarm Reset ............................................................ 4-9
When an Alarm Occurs ........................................... 4-9
Chapter 5 Measuring CO2 .................................................. 5-1
Introduction ............................................................ 5-1
Safety Information .................................................. 5-1
Monitoring Procedure ............................................. 5-2
CO2 Display ........................................................... 5-6
Respiratory Rate ...................................................... 5-7
Setting CO2 ............................................................. 5-7
CO2 Zero .............................................................. 5-10
Calibration ............................................................ 5-11
Removing Exhaust Gases from the System ........... 5-12
Chapter 6 Measuring SpO2 ................................................ 6-1
Introduction ............................................................ 6-1
Safety Information .................................................. 6-2
Monitoring Procedure ............................................. 6-4
SpO2 Display .......................................................... 6-5
PR Display .............................................................. 6-6
Setting SpO2 ........................................................... 6-7
Setting Desat Limit ................................................. 6-8
Chapter 7 Trend Review ..................................................... 7-1
Introduction ............................................................ 7-1
Review Interface ..................................................... 7-1
Review Setup .......................................................... 7-2
Chapter 8 Battery ................................................................ 8-1
Introduction ............................................................ 8-1
Charging the Battery ............................................... 8-2
Optimizing Battery Performance ............................. 8-2
Checking the Lithium Battery ................................. 8-3
Disposing of the Batteries ........................................ 8-4
Chapter 9 Maintenance and Cleaning ................................ 9-1
Introduction ............................................................ 9-1
Seasonal Safety Checking ....................................... 9-2
Cleaning the Monitor .............................................. 9-4
Cleaning SpO2 Sensor ............................................ 9-5
Disposal .................................................................. 9-5
Chapter 10 Accessories ..................................................... 10-1
VIII
Appendix A Product Specifications ........................................ 1
Safety Specifications .................................................... 1
Physical Specifications ................................................ 1
Environmental Specifications....................................... 2
Charging Specifications ............................................... 2
Hardware Specifications .............................................. 3
Data Storage ................................................................ 4
Measurement Specifications ........................................ 5
Appendix B Factory Defaults ................................................. 9
Alarm Setup ................................................................. 9
System Setup ................................................................ 9
CO2 Setup .................................................................. 10
SpO2 Setup ................................................................ 10
Trend Setup ................................................................ 10
Appendix C Alarm Message .................................................. 11
Physiological Alarm .................................................... 11
Technical Alarm ................................ ......................... 12
Prompt Message ......................................................... 14
Appendix D EMC ................................................................. 15
Appendix E Warranty Registration Card ........................... 16
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1-1
Chapter 1 General Introduction
Intended Use
LifeVet CP patient monitor is intended for continuously
monitoring or spot checking of CO2, RR, SpO2 and PR signals
in animals.
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.
Main Unit
Front View
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1-2
6 1
2
5
3
4
Fig 1-1 Front View of the Monitor
1. Alarm indicating lamp
When an alarm occurs, this lamp will light up as defined
below:
• High level alarm: the lamp quickly flashes red.
• Medium level alarm: the lamp slowly flashes yellow.
• Low level alarm: the lamp lights yellow without
flashing.
2. Display screen
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1-3
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 “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
Rear View
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Fig 1-2 Rear View of the Monitor
Side View
Topside:
1 2
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Downside:
3
Rightside:
4
5
Fig 1-3 Side View of the Monitor
1. CO2 connector
2. SpO2 probe connector
3. Micro USB connector
• Connect with power adapter.
4. Shortcut key
Press this button to start or pause the CO2 measurement.
5. Power buttom
• Press it about two seconds to turn on when the monitor is
on the condition of shutdown.
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• 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.
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.
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Multi-Parameter Display Mode
6
8
7
5
4
3
2
1
9
10
Fig 1-4 Multif-parameter Display Mode
1. Patient ID No.: Click and set patient information, its range
from 1 to 96.
2. SpO2 parameter area: The current SpO2 and its higher
and lower alarm limits are shown in the area.
3. SpO2 waveform area: The waveform shown in the area is
current SpO2 volume curve.
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1-8
4. CO2 parameter area: The current CO2 and its higher and
lower alarm limits are shown in the area
5. CO2 waveform area: CO2 waveform is shown in the area.
6. Physiological alarm area: Current physiological alarm
information is shown in the area.
7. Technical alarm and prompt information area: Current
technical alarm and prompt information are shown in the
area.
8. Alarm status area: Alarm status symbols are shown in the
area.
9. System time: Current time is shown in the area.
10. Battery symbol: The symbol indicates the current quantity
of electricity of batteries and whether the device is
connecting power source, the alternating-current symbol
is above battery symbol when the device is connecting
power source.
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SpO2 Display mode
1
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
current SpO2 value and its higher 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.
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CO2 Waveform Display Mode
1
2 3
Fig 1-6 CO2 Display Mode
1. CO2 waveform display area: Waveform shown in the area
is current CO2 waveform 。
2. CO2 parameter area: The values shown in the area are
current HR value and its higher and lower alarm limits.
3. RR parameter area: The values shown in the area are
current RR value and its higher and lower alarm limits.
LifeVet CP User Manual
2-1
Chapter 2 Safety
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.
• When the monitor is connecting with high-frequency
devices, sensors and cables should avoid touching
high-frequency devices, in order to leakage current
burns patient.
• Keep the monitor away from dust, vibration,
corrosive substances, explosive materials, high
temperature and moisture.
LifeVet CP User Manual
2-2
• 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
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.
• 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
LifeVet CP User Manual
2-3
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
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。
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
LifeVet CP User Manual
2-4
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 the electrodes are used and placed
properly, the display of the monitor will be restored
within 10s. 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.
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2-5
• This manual describes all features and options. Your
monitor may not have all of them.
Explanation of Symbols
Symbol
Symbol Note
Type CF applied part, defibrillation protected
The unit displaying this symbol contains an F-Type
isolated (floating) applied part providing a high
degree of protection against shock, and is
defibrillator-proof.
Refer to User Manual.
Alternating current
IPX1
Degree of protection against ingress of liquid
Alarm volume off
Alarm paused
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2-6
Alarm reset
QRS volume off
Date of manufacture
Manufacturer
Serial number
Power button
CO2
Short for “Carbon dioxide”
RR
Short for “Respiratory Rate”
SpO
2
Short for “Pulse Oxygen Saturation”
Symbol for the marking of electrical and
electronics devices according to Directive
2002/96/EC.
LifeVet CP User Manual
3-1
Parts
Standard
Optional
Quantity
CO2 nose sampling
tube
√
1
CO2 filter
√
1
SpO2 probes
√
1
User Manual
√
this
manual
QC certificate
√
1
Packing list
√
1
Power adapter
√
1
USB data cable
√
1
Carrying case
√
1
Suction mount
√
1
Chapter 3 Basic Operations
Unpacking and Checking
Open the package. Parts are as follows in the package .Take
out the monitor and its accessories.
Getting Started
Before you start to make measurements, carry out the
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3-2
following checks on the monitor including all connected
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.
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.
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3-3
Screen Brightness Setting
【Menu】→【System】，click the right of 【Brightness】，
you can set the screen brightness to a value between 1to 5,
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.
Auto-Rotate Setting
【Menu】→【System】，click the right of 【Auto-rotate】
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.
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:
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2. Select 【 Date Format 】 , it can be set to
【 Year/Month/Day 】 、 【 Month/Day/Year 】 or
【Day/Month/Year】.
3. Select【Time Format】, it can be set to【24h】or【12h】.
4. Set the current date and time and select【OK】to confirm
it.
Patient Information Setting
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【Horse】,【Dog】or【Cat】.
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.
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3-5
Demo Mode Setting
To enter the demo mode:
Select 【Menu】→【System】→【Maintenance】→enter
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.
Language Setting
Select 【Menu】→【System】→【Maintenance】, enter the
required password. On 【Factory Mainten.】interface, you can
select 【Language】and then choose a desired language.
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3-6
Checking the Version
Select【Menu】→【System】to check the version of the
monitor .
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. Selec【t Set to Default】, popping up a confirming window,
select【OK】to restore the factory configuration.
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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3-7
【System】→【Maintenance】, enter the required password,
click the right of 【Auto power-off setting】, you can select
“off”, “10min”, “30min”.
LifeVet CP User Manual
4-1
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.
Q?
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.
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.
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4-2
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.
Alarm Levels
1. By severity, the monitor’s physiological alarms can be
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
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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 four categories: high level, medium level
alarms, low level alarms and prompt message.
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.
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
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4-4
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.
Alarm Tone
The different level alarms are indicated by the system in
following different audio ways:
Alarm
level
Audible prompt
High “DO-DO-DO------DO-DO,DO-DO-DO------DO-DO”
Medium
“DO-DO-DO”
Low “DO-”
Alarm Lamp
When an alarm occurs, the alarm levels are indicated in the
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4-5
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.
Low
Alarm lamp lights on in yellow without
flashing.
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.
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: ***
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4-6
Medium level alarms: **
Low level alarms: *
◆ The system uses different background colors for the alarm
message to match the alarm level:
High level alarms: re d
Medium level alarms: yellow
Low level alarms: yellow
Prompt message: blue
Flashing Numeric
When a physiological alarm occurs, the numeric of
parameter will flash.
Alarm Status Symbol
To identify the control for alarm paused or to
indicate that the alarm system is in the alarm
system is in the alarm paused state.
indicates the alarm sound is turned off.
To identify the control for alarm reset.
Alarm Tone Configuration
1. The minimum alarm volume setting.
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4-7
Select 【Menu】→【System】→【Maintenance】, enter
the required passwo d, select 【Machine Mainten.】→【Alarm
Setup】→【Min.Alm.Vol.】, you can select “ Off, High, Mid,
Low”.
2. Alarm volume setting
Select 【Menu】→【System】→【Alarm Volume】, you
can select from X to 4. X indicates the minimum alarm volume.
Pausing Ala rms
Press the button
on the front panel of monitor, you can
suspend all alarm indicators of the monitor:
• The visual alarm and audible alarm are all suspended.
• The parameters of physiological alarm stop flashing.
• The alarm message in the physiological alarm area will not
be displayed.
• The remaining time and the icon will be shown in the
physiological alarm area.
After the alarm paused time, the monitor will automatically
cancel the alarm pausing. Press again the button
pausing can be cancelled by manual operation.
, the alarm
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4-8
Shutting off the Alarm Volume
Set the 【Min.Alm.Vol.】and【Alarm Volume】to 【off 】
to shut off the alarm volume. 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 off. The
audible alarm is reactivated automatically when:
• The factory configuration is finished;
• Set the alarm volume to a non-off 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:
• When the alarm sound is switched off, the monitor will
give no audible alarm tones even if a new alarm occurs.
Therefore the user should be very carefully about
whether to switch off the alarm sound or not.
• Don’t rely exclusively on the audible alarm system for
patient monitoring. Adjusting alarm volume to a low
level may result in a hazard to the patient. Always
keep the patient under close surveillance.
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4-9
Alarm Reset
Select 【Menu】→【System】→【Maintenance】→enter
the required passwo d, select 【Machine Mainten.】→【Alarm
Setup】. You can turn on alarm reset. Alarm reset will be
displayed on the interface of system.
Select 【Menu】→【System】→【Alarm reset】.
After licking alarm reset :
• You can reset current alarm system, it will exit alarm pause
if it is on the condition of alarm pause.
• It only turns off audible alarm, the visual is going on for the
existing alarm.
When an Alarm Occurs
Q?
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.
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4-10
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.
LifeVet CP User Manual
5-1
Chapter 5 Measuring CO2
Introduction
The monitor adopts infrared absorption technology to measure
the carbon dioxide (CO2) concentration in the breathing airway of
patient. Because CO2 molecule can absorb infrared light of special
wavelength, and the amount of absorbed infrared light directly
relates to the concentration of CO
2,
therefore while the infrared
light radiated from the infrared light source passing through the
gas sample containing CO2, part of energy will be absorbed by
CO2 in the gas. At another side of infrared light source, a
photodetector is used to measure the remaining infrared energy
and convert it to electric signal, which will be compared with the
energy of infrared light source and adjusted so as to correctly
reflect the CO2 concentration in the gas sample.
Sidestream: Takes a sample of the respiratory gas with a
constant sample flow from the patient’s airway and analyzes it
with the CO2 sensor.
Safety Information
:
Warning:
• Do not position the sensor cables or tubing in any
LifeVet CP User Manual
5-2
manner that may cause entanglement or strangulation.
• Performance is not guaranteed if an item labeled as
single patient use is reused.
• Monitor the CO2 waveform (Capnogram). If you see
changes or abnormal appearance check the sampling
tube. Replace it if needed.
• Monitor the CO2 waveform (Capnogram) for elevated
baseline. Elevated baseline can be caused by sensor or
patient problems.
• Do not operate the CO2 module when it is wet or has
exterior condensation.
• Do not use device on patients that cannot tolerate the
withdrawal of 50 ml/min±10 ml/min from the airway
or patients that cannot tolerate the added dead space
to the airway.
• Do not connect the exhaust tube to the ventilator
circuit.
Monitoring Procedure
1. The measurement value will be more accurate if the
monitor has 2 minutes’ warming-up time. To connect the
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5-3
CO2 filter with 3-way joint of the loop of anesthetic
machine by sampling tube, or to directly connect patient’s
nose by the hose.
Fig 5-1-1 Connection of Sampling and Filter
LifeVet CP User Manual
5-4
Fig 5-1-2 Connection of Sampling with 3-way joint or
patient’s nose
Q?
Note:
• Inserting the sampling tube into the receptacle
automatically starts the sampling pump. Removal of
the sampling tube turns the sample pump off.
• To remove the CO2 filter from CO2 connector, press
and rotate anticlockwise the filter, and then pull out
filter.
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5-5
2. Connect CO2 filter into CO2 connector and rotate CO2
filter closewise.
3. Connect sampling tube into CO2 filter. If the sampling
tube is occluded or damaged, perform a “Check sampling
line” on screen..
4. Ensure that the CO2 sensor exhaust tube vents gases away
from the sensor environment.
5.
Using the shortcut key on the right of monitor to
start or pause CO2 measurement.
Caution:
• Always disconnect the filter from the CO2 connector
when not in use.
• Do not insert the things other than filter into CO2
connector.
• The sampling tubes are disposable. Please keep the
sampling tube clean, and prevent the tube from
clogging by dust. It is advised to replace the sampling
tube every 12h (up to 120h of use with filter tip), the
sampling tube leaks or has been damaged and
contaminate .
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5-6
CO2 Display
• CO2 parameter display
1
5
2
4
3
Fig 5-2 CO2 Display
1.CO2 label 2.CO2 high alarm limit
3. CO2 low alarm limit 4. CO2 value
5. CO2 unit
• CO2 waveform display
Fig 5-3 CO2 Waveform Display
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5-7
Respiratory Rate
1
5
2
4
3
Fig 5-4 RR Display
1. RR label 2. RR higr alarm limit
3. RR low alarm limit 4. RR value
5. RR unit
Setting CO2
Select 【Menu】→【CO2 Setup】, enter into CO2 setup
interface.
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5-8
Fig 5-5 CO2 Setup Interface
Setting CO2 and RR Alarm
Click the right of 【Alarm】, you can set CO2 and RR
Alarm , you can select “Mid, High”.
Setting CO2 and RR Alarm Limits
Click the right of 【Uplimit】or 【Downlimit】, you can set
up limit and down limit of CO2 and RR. Attention: The high
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5-9
alarm limit should greater than the lower one.
Setting CO2 Scan Speed
Select scan speed of CO2 waveform. Click the right of
【Speed】, you can select “6.25 mm/s、12.5mm/s, 25 mm/s”.
Setting CO2 Unit
Click the right of【CO2 Unit】, you can select “mmHg、%、
kPa”.
Setting Scale
You can adjust the position of wave scale manually, and the
waveform amplitude will vary along with it. Click the right of
【Scale】, you can select “61mmHg、76mmHg、91 mmHg、
106 mmHg”.
Setting Apnea Alarm
You can select the apnea time as required in the options. The
monitor indicates an alarm when a pre-adjusted time has elapsed
since the last detected breath. Click the right 【Apnea Alm】,
you can select “Off, 5s, 10s, 20s, 40s, 60s, 80s, 100s, 120s”.
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5-10
CO2 Zero
While zeroing is recommended the first time the monitor is
connected to the filter, it is only absolutely necessary when the
message “Zero Required” is displayed.
Follow these steps:
1) Ensure that the sampling tube is not connected to the
patient or close to any source of CO2 (including the
patient's, your own, exhaled breath and ventilator exhaust
valves).
2) Select 【Menu】→【System】→【Maintenance】, enter
password.
3) Select 【Machine Mainten.】→【CO2 Setup】→【CO2
Zero】,The unit zeroes the module and displays the Zero
In Progress message for approximately 15-20 seconds.
The message disappears upon completion of the zeroing.
Caution:
• Always ensure that the filter is properly connected to
the CO2 connector before zeroing.
• Do not attempt zeroing for 20 seconds after removing
the sampling tube from the patient’s airway. This time
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5-11
allows any CO2 remaining in the sampling tube to
dissipate before zeroing.
• Do not attempt to zero the monitor while the sampling
tube is in the patient’s airway.
• Do not attempt zeroing if the temperature is not stable.
• Zeroing with CO2 in sampling tube can lead to
inaccurate measurements or other error conditions. If
you attempt zeroing while CO2 remains in sampling
tube, the time required to zero the monitor may be
increased.
Calibration
The monitor has already been calibrated before leaving
factory. User can directly apply it to measuring in normal
conditions, to the exclusion of the below conditions.
For Sidestream CO2 module, please carry out gain calibration
and manual offset calibration, when the following conditions
happened:
——The module has been used for between half a year and
one year.
——The accuracy of CO
2
reading has been doubted by clinical
physician.
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5-12
——After the latest calibration, atmospheric pressure or height
above sea level varies evidently.
Caution:
User may only calibrate the device under the
instruction of the technical personnel authorized by
manufacturer. Moreover, incorrect calibrating
procedure may result in incorrect reading.
Removing Exhaust Gases from the
System
:
Warning:
When using the SidestreamCO2 measurement on
patients who are receiving or have recently received
anesthetics, connect the outlet to a scavenging system,
or to the anesthesia machine/ventilator, to avoid
exposing medical staff to anesthetics.
This monitor removes exhaust gas to outside directly.
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6-1
Chapter 6 Measuring SpO2
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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6-2
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 cats, 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
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6-3
errors, and certain patient conditions. See the
appropriate sections of this manual for specific safety
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.
Q?
Note:
• The pleth wave is not equal to the intensity of PR
signal.
• The monitor does not provide automatic self-
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6-4
examination alarm signal and the operator has to use
SpO2 simulator for self-examination.
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 patient
Place the sensor on the tongue or ear of the animal. The preferred
sensor application site for dogs, cats and horses is on the tongue
with the optical components of the sensor positioned at the
center of the tongue. Alternatively, the sensor and the clip may
be applied to the lip, toes, ear, foreskin or vulva of the animal.
:
Warning:
• Do not use the SpO2 sensor on a limb where the NIBP
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6-5
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.
SpO2 Display
• Parameter Display
1 5
2
4
3
Fig 6-1 SpO2 Parameter
1. SpO2 label 2. High alarm limit of SpO
2
3. Low alarm limit of SpO
2
4. SpO2 value
5. SpO2 unit
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6-6
• Waveform Display
Fig 6-2 SpO2 Volume Curve
PR Display
1
5
2
4
3
Fig 6-3 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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6-7
Caution:
During the monitoring of HR and PR, displaying of HR
has priority. That is PR will be displayed only when there
isn’t HR monitoring.
Setting SpO2
Select 【Menu】→【SpO2 Setup】, enter into SpO2 Setup
interface.
Fig 6-4 SpO2 Setup
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6-8
Setting SpO2 Alarm
Click the right of 【Alarm】, you can set alarm level of SpO
2
and PR, you can select “Mid, High”
Setting SpO2 Alarm Limits
Click the right of 【Uplimit】or 【Downlimit】, you can set
the SpO2 uplimit and downlimit. Attention: The high alarm limit
should greater than the lower one.
Setting Scan Speed
Click the right of 【Speed】, you can select “6.25 mm/s、
12.5mm/s, 25 mm/s”.
Setting Average Time
Click the right of【Avg Time】, you can select “4s, 8s, 16s”.
Setting QRS Volume
Click the right of【QRS Vol.】, you can select “Off, High,
Mid, Low”.
Setting Desat Limit
SpO2 desat means when SpO2 measuring value is lower than
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6-9
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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Chapter 7 Trend Review
Introduction
Select 【Menu】→【Trend】to enter trend reviewing
window. In the window, you can review CO2, RR, SpO2 and PR
data stored before.
Review Interface
Fig 7-1 Review Interface
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7-2
If the trend date is not only one page, you can turn pages
by the next/return button.
Review Setup
Click the right of 【ID】to select patient’s ID, you can
review patient’s trend review by selecting different ID.
Fig 7-2 ID Review Interface
Click the right of 【More】on the top of review interface, the
drop-down window shown as following:
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7-3
Fig 7-3 The drop-down Window of “More”
You can set 【Save time】, 【Delete】, 【Delete all】,
【Transmission】in this interface.
• Save time: To adjust recording time, you can select”10s,
30s, 1min, 2 min, 5min, 10min”.
• Delete: To delete trend data of the selected ID No.
• Delete all: To delete trend data of all patients.
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Chapter 8 Battery
Introduction
A rechargeable and maintenance-free battery is designed for
Patient Monitor, which enables continuous working when AC
power off.
When r a lithium ion battery is used, the battery icon
indicates the battery status as follows:
1. Indicates that the power of the battery is full；
2. Indicates that the power of the battery is 3 grids left；
3. Indicates that the power of the battery is 2 grids left；
4. Indicates that the power of the battery is 1 grid left；
5. Indicates that the battery is almost depleted.
Battery power supply can only last for a period of time. If
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.
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8-2
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.
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
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.
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8-3
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.
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
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.
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8-4
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 9 Maintenance and Cleaning
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 acetonebased 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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9-2
Caution: If you spill liquid into the equipment of
accessories, connect you service personal or us.
Seasonal Safety Checking
Q?
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
functional damage.
② Inspect the safety relevant labels for legibility.
③ Verify that the device functions properly as described in the
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9-3
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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9-4
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 a warm environment for several hours until it is
completely dry. Never use a wet or humid cable/plug!
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9-5
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.
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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Chapter 10 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
Mode
PN
CO2
CO2 Filter
15-100-0184
CO2 Tube
15-100-0035
3-Way Joint
15-100-0037
Horse/ Dog nose sampling
tube
15-100-0187
SpO2 sensor
usable，Horse
15-100-0013
usable，Dog
15-100-0014
usable，Cat
15-100-0015
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1
Appendix A Product Specifications
Safety Specifications
CFDA classification
II
CE classification
IIb
Type of protection against electric
shock
II, with internal power or
external power device
Degree of protection against
electric shock
CF
Degree of protection against
hazards of explosion
Ordinary equipment, without
protection against hazards of
explosion
Degree of protection against
ingress of liquid
IPX1
Equipment type
Handheld
Mode of operation
Continuous
Physical Specifications
Mainframe weight
500g (full configuration, including the
batteries)
Mainframe size
142mm(W)×78mm(H)×36mm(D)
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2
Environmental Specifications
Temperature
Operating: 5℃ to +40℃；
Storage: -20℃ to +55℃；
Atmospheric
pressure
Operating: 860hPa to 1060hPa；
Storage: 500hPa to 1060hPa；
Humidity
Operating: 15% to 85%(non condensing)
Storage: 10% to 93%(non condensing)
Charging Specifications
A4.1 Charger
Micro USB
Charge
Power adapter
Input: AC 100～240Ｖ
Output: DC 5V/2A
A4.2 Battery Requirement
Type
Built-in lithium battery
Voltage
3.7V
capacity
4800mAH
Charging time
3～4h
Run time
>18h
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3
Hardware Specifications
Display
Size
4.3inch
Resolution
480*272
Touch
Resistive touch
Autorotation
Direction
four direction
Indicating Lamp
Alarm indicating
1 (Yellow/Red), on the top of screen
Battery charging
indicating lamp
1 (orange）
When charged, it lights orange.
When fully charged or not charged, it
doesn’t light.
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
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4
Patient ID
1～96
Display way
Trend tabular
SpO2 trend
interval
10s 、 30s 、 1min 、 2min 、 5min 、
10min
Storage
Save when power down
60601-1-8.
Alarm pressure
45 dB to 85 dB, Testing place is 1 meter
from the tone.
Buttons
Power button
Turn on/off
Shortcut key
Start/Pause CO2 measurement
Short press to achieve the above function，
long press + power button to achieve
calibration of LCD
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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5
Capacity
500 groups/patient can be stored (only
data, no waveform).
Measurement Specifications
CO2 Specifications
CO2 (Sidestream)
Measureme
nt Way
Infrared spectrum
Measureme
nt Range
0—19.7% (0-150mmHg or 0-20.0kPa )
CO2
Accuracy
0%-5.3% (0mmHg-40mmHg),±0.3% (±2mm
Hg)；
5.4%-9.2% (41mmHg-70mmHg), ±5% of
reading；
9.3%-13.2% (71mmHg-100mmHg);±8% of
reading；
13.3%-19.7% (101mmHg-150mmHg), ±10%
of reading.
CO2
Resolution
0.1mmHg
Gas Flow
Rate
60~80ml/min
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6
Unit
%, mmHg, kPa
Measureme
nt Range of
awRR
3~150 rpm
Measuring
accuracy of
RR
±1% or ± 1 rpm, whichever is greater
Response
Time
＜3s
Calibration
Offset calibration, auto/ manual; gain
calibration
CO2 Alarm
Range
0—19.7%( 0-150mmHg or 0-20.0kPa )
high/low limit can be adjusted continuously
Alarm
Indication
Blinking display of the data and parameters,
text prompts, Three levels of alarming:
sound-light alarming, alarming with blinked
data and parameters, and that with text
prompts.
SpO2
SpO
2
Measurement
0~100%
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7
range Resolution
1%
Accuracy
70~100%：± 2%
Alarm
Select the high and low alarm limit of
SpO
2
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
period
13s
Anti-interference
Anti-motion interference
Anti-electrotome interference
Resisting low
perfusion ability
With powerful ability of resisting low
perfusion, PR amplitude can reach to
0.2% with value of SpO2 displaying.
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8
Pitch Tone
with
PR
Measuremen
t range
25 bpm ~250 bpm
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.
Alarm Setup
Alarm Setup
Factory Default
Alarm volume
Medium
Minimum alarm
volume
Low
SpO2 Alarm Level
Medium
CO2 Alarm Level
Medium
System Setup
System setup
Factory Default
QRS volume
medium
Brightness
3
Scan speed
12.5mm/s
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10
CO2 Setup
CO2 setup
Horse
Dog
Cat
EtCO2 High Limit
62 mmHg
62 mmHg
62 mmHg
EtCO2 Low Limit
21 mmHg
21 mmHg
21 mmHg
RR
Horse
Dog
Cat
RR High Limit
35 rpm
40 rpm
40 rpm
RR Low Limit
5 rpm
8 rpm
8 rpm
SpO2 Setup
SpO2 Setup
Horse
Dog
Cat
SpO2 High Limit
100 %
100 %
100 %
SpO2 Low Limit
90 %
90 %
90 %
PR Setup
Horse
Dog
Cat
PR High Limit
50 bpm
160 bmp
200 bpm
PR Low Limit
30 bpm
70 bpm
90 bpm
Trend Setup
Trend Setup
Factory Default
Interval
30s
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Appendix C Alarm Message
This section lists some important alarm message. In the tables
below, “*” means the alarm level is user-adjustable.
Physiological Alarm
SpO2
Alarm Messages
Cause
Level
SpO2 Too High *
A measurement has risen
above the high alarm limit
or fallen below the low
alarm limit
High、
Medium
SpO2 Too Low *
High、
Medium
PR Too High *
High、
Medium
PR Too Low *
High、
Medium
SpO2 Desat
SpO2 measurement has
fallen below the SpO2 desat
limit.
High
No Pulse
The pulse signal was too
High
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weak to be analyzed.
CO2
Alarm Messages
Cause Level
EtCO2 Too High
*
A measurement has risen
above the high alarm limit
or fallen below the low
alarm limit.
High、
Medium
EtCO2 Too Low *
High、
Medium
RR Too High
High、
Medium
RR Too Low
High、
Medium
Apnea
Resp can’t be detected on
preset-time.
High
Technical Alarm
Message
Cause
Level
SpO2 Sensor Off
The SpO2 sensor detached
the patient or the monitor.
Low
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CO2 Sensor Off
The CO2 sensor detached the
patient or the monitor.
Low
Communication
Error
Communication error or test
model error.
Low
Battery Low
The battery power is low.
Medium
SpO2 Low Perf
The signal detected is weak.
Medium
CO2 measurement
over range
CO2 measurement Over
range, need ve rify zero
Low
CO2 sensor error
CO2 sensor error.
Low
CO2 sensor Over
Temp
Temperature of the sensor is
over the normal working
temperature.
High
Check CO
2
Sampling Line
Sampling line is occluded or
damaged.
Sampling tube is kinked or
pinched.
Exhaust tube is blocked.
Low
Zero Required
The sensor needs verify zero.
High
CO2 sensor no
initialized
CO2 sensor no initialized
Low
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Prompt Message
Message
Cause
Level
searching
Searching pulse
Prompt
Message
SpO2 sensor off
SpO2 sensor may be
disconnected from the
patient or the monitor.
Zero in Progress
Zeroing is in progress.
CO2 sensor off
Sensor dose not connect
with monitor when the
monitor is running.
After confirming alarm
message of sensor off, the
alarm message will become
prompt message.
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Appendix D EMC
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Appendix E Warranty Registration
Card
Thank you for purchasing EICKEMEYER® products!
Please complete this card and mail back to EICKEMEYER
KG 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 EICKEMEYER®.
Product
Model
Serial No.
Contract
Date Installed
Warranty
Name
Address
Contact
Person
Tele/fax
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