Contec Medical Systems CONTEC08A-BT Electronic Sphygmomanometer (Blood Pressure Monitor) User Manual
Contec Medical Systems Co., Ltd. Electronic Sphygmomanometer (Blood Pressure Monitor) Users Manual
Users Manual
I
Foreword
Please read the User Manual carefully before using this product. The User Manual which
describes the operating procedures should be followed strictly. This manual detailed
introduce the steps must be noted when using the product, operation which may result in
abnormal, the risk may cause personal injury and product damage and other contents, refer to the
chapters for details. Any anomalies or personal injury and device damage arising from use,
maintain, store do not follow requirements of the User Manual, Our company is not responsible
for the safety, reliability and performance guarantees! The manufacturer’s warranty service does
not cover such faults!
Note: Please read the User Manual carefully before using this product.
Described in this User Manual is in accordance with practical situation of the product. In case of
modifications and software upgrades, the information contained in this document is subject to
change without notice.
The warning items
Before using this product, you should consider the safety and efficacy of the following
described:
The safety classification of this product is class Ⅱ equipment, type BF.
Described each measurement results combined with clinical symptoms by qualified doctors.
The reliability and operation of using this product whether meets the operation of this
manual relate to the maintenance instructions.
Warning: Replace accessories which not provided by our company may lead to the
occurrence of errors.Without our company or other approved maintenance organizations
trained service personnel should not try to maintain the product.
Responsibility of operator
The operator must carefully read the User Manual before use this product, and strictly
follow the operating procedure of the User Manual
Fully consider the security requirements during product design, but the operator should not
ignore the observation for the patient and the state of machine.
The operator has the responsibility to provide the use condition of the product to our
company.
Responsibility for our company
Our company have the responsibility to provide qualified product which conform to
company standard of this product.
Our company have the responsibility to complete product installation, debugging and
technical training according to the contract.
Our company have the responsibility to complete product maintenance according to the
contract.
Our company have the responsibility to respond the requirements of user in time.
The User Manual is writen by our company. All rights reserved.
II
Contents
Chapter1 Functions and Purpose ............................................................................................. 1
Chapter2 Safety Precautions ................................................................................................... 2
2.1 Operation about AC Adapter ..................................................................................... 3
2.2 Operation about Batteries .......................................................................................... 4
Chapter3 Main Unit ................................................................................................................ 5
Chapter4 External Interfaces ................................................................................................... 7
Chapter5 Dry Battery/AC Adapter Installation ....................................................................... 8
5.1 Dry Battery Installation ............................................................................................. 8
5.2 Using the AC adapter ................................................................................................ 8
Chapter6 Button Functions ................................................................................................... 10
Chapter7 Set Date and Time ................................................................................................. 11
Chapter8 Unit and Language ................................................................................................ 13
8.1 Measurement Unit ................................................................................................... 13
8.2 Language ................................................................................................................. 13
Chapter9 Alarm Function ........................................................................................................ 1
9.1 Physiological Alarm .................................................................................................. 1
9.2 Technical Alarm ........................................................................................................ 1
Chapter10 Measurement Mode ............................................................................................... 2
Chapter11 Application of the Sphygmomanometer ................................................................ 3
11.1 Accurate Measurement Way .................................................................................... 3
11.2 Applying the Cuff .................................................................................................... 3
11.3 BP Measurement ..................................................................................................... 4
Chapter12 Memory Fuction .................................................................................................... 6
12.1 Read Memory Values .............................................................................................. 6
12.2 Delete Memory Values ............................................................................................ 7
Chapter13 Bluetooth Data Sending ......................................................................................... 8
Chapter14 SpO2 Measurement Function ................................................................................. 9
Chapter15 SpO2 Measurement Method ................................................................................. 11
Chapter16 Maintenance, Cleaning and Keeping ................................................................... 12
Chapter17 Error Message ...................................................................................................... 14
Chapter18 Troubleshooting ................................................................................................... 15
Chapter19 Meanings of Symbols .......................................................................................... 16
Chapter20 Specification ........................................................................................................ 17
1
Chapter1 Functions and Purpose
Description of functions:
The Sphygmomanometer apply to measure the non-invasive blood pressure of human (adult,
pediatrics, neonate), each user can store 100 items records of measurement results at most. Each
record includes detailed measuring time, systolic pressure, diastolic pressure, average pressure,
pulse rate and record number, etc. With 2.8 inch color LCD screen, clear interface, the function
of data review is complete. User can implement ON/OFF, manual measuring, system setup,
parameters change and other operations with seven buttons which are located on the front panel
of the device. The device uses audible and visual alarm, when the battery power is low, the
buzzer will intermittent buzzing and LCD screen displays "Low Power" to prompt user replace
batteries. When the measurement data exceeds the set alarm limit, the font color of measurement
results will change to red and the audible alarm will occur, user can open and close the alarm
sound according to needs. Users can send measurement results which be automatically saved by
device to mobile phone with bluetooth transmission function. Refer to the help or explication of
the related software for specific operation.
Purpose:
The device apply to measure the non-invasive blood pressure and SpO2(optional) of human.
Record parameter value of blood pressure to provide the reference for the health care
professional
2
Chapter2 Safety Precautions
●Before use, carefully read the "Safety Precautions" for a correct use.
●To prevent users suffered hurt or damnification due to improper use,see "Safety
Precautions",and use this product properly.
For safety reasons, be sure to comply with safety precautions.
Note
Human and the surrounding environment are in the range of electromagnetic radiation
which generated by this device,there is no energy hazard to human or the surrounding
environment, also not affected by the electromagnetic interference of the external device.
This device has slight energy radiation,should be avoided too close to the high precision
re
q
uirements e
q
ui
p
ment.
Note
If not to use correctly, it exists that a potentially hazardous situation which may result in
injury to the user or patient or damage to the equipment or other property.
3
2.1 Operation about AC Adapter
Note
Please use the dedicated AC adapter of this device.
Otherwise it may cause trouble.
Dedicated AC adapter must use AC 100V~220V.
Otherwise it may cause fire or electric shock.
When there is breakage of dedicated AC adapter plug or wire,please do not use it.
Otherwise it may cause fire or electric shock.
Please do not plug or unplug the adapter on the socket with wet hands
Otherwise it may cause electric shock or injury.
Note
Self-diagnosis and treatment using measured results may be dangerous.Follow
the instructions of your physician.
Please hand measurement results to the doctor who know your health to accept
diagnosis.
For severe blood circulation disorder or arrhythmia patients, please use the
device under the guidance of a doctor.
Otherwise it may lead to acute hemorrhage, or measurement error as a result of squeezed
arm.
Infant and the person who can't express oneself can't use the device
Otherwise it may cause accident or dissension
Please do not use for any other purpose.
Otherwise it may cause accident or holdback.
Please use special cuff.
Otherwise it is possible that measurement result is incorrect.
Please do not keep the cuff in the over-inflated state for a long time
Otherwise it may cause risk
Do not disassemble,repair and change the device
Otherwise it can not measure correctly
4
2.2 Operation about Batteries
Advice
Do not subject the device to strong shocks, such as dropping the unit on the floor;
Do not inflate before the cuff wrapps around the arm;
Do not inflect the cuff and the air tube forcibly.
Note
Please use 4 "AA" manganese or alkaline batteries, do not use batteries of other
types.
Otherwise it may cause fire.
New and old batteries, different kinds batteries can not be confusion.
Otherwise it may cause battery leakage, heat, rupture, and damage to Electronic
Sphygmomanometer.
Please don't put wrong the positive and negative of battery. When the batteries
power exhausts, replace with four new batteries at the same time.
Please take out the dry batteries when you do not use the device for a long time.
Otherwise it may cause battery leakage, heat, rupture, and damage to Electronic
Sphygmomanometer.
If electrolyte of the batteries immodestly get in your eyes, immediately rinse with
plenty of clean water.
It will cause blindness or other hazards,Should immediately go to the nearest hospital
for treatment
If electrolyte of the batteries immodestly glues on the skin or the clothes,
immediately rinse with plenty of clean water.
Otherwise it ma
y
hurt the skin.
5
Chapter3 Main Unit
(Cuff specification: limb circumference 22-32cm (middle part of upper arm))
User Manual
Optional Accessories:
AC adapter
Input: voltage: AC 100V~220V
frequency: 50Hz/60Hz
Rated current:AC 150mA
Output: DC 6.0V±0.2V 1.0A
or DC5.0V±0.2V 1.0A
On /Off button
Start /stop button
Cuff Plug
Cuff Air Plu
g
Dis
p
la
y
Up/Down button
Memory button
AC adapter socket
Menu button
USB socket
Accessories:
Adult Cuff Dry Battery
6
SpO2 Probe: Y10UCH150
A. SpO2 measurement
Range:0%~100%
Error: 70~100%:±2%;Below 70%:unspecified
B. Pulse rate measurement
Range:30bpm~250bpm
Error: ±2bpm or ±2%(select the larger)
C. Optical sensor: red light(wavelength: 660nm,
6.65mW) infrared light(wavelength: 880nm, 6.75mW)
7
Chapter4 External Interfaces
Note
Please hold the air plug to remove the NIBP cuff.
Note
The cuff socket and AC adapter socket of the sphygmomanometer only connect to the
stated equipment which accord with the requirements of IEC 60601-1: 1988 “Medical
electrical equipment-Part 1: General requirements for safety”.
①Cuff Socket
Left side
The right side of the device is USB socket
and AC adapter socket
USB socket
AC adapter socket
Right side
8
Chapter5 Dry Battery/AC Adapter Installation
This product can use dry batteries as well as AC adapter.
5.1 Dry Battery Installation
① Demount the battery cover in the direction of the arrow.
② Install "AA" dry batteries according to polarities.
③ Slide to close the battery cover.
Icon “ ” : the batteries power will exhaust. Replace with four new batteries (the same
sort) at the same time. Test while low power may cause data deviation and other problems.
Turn the unit off before replacing the batteries.
Note
Dispose of the batteries according to applicable local regulations about environmental.
5.2 Using the AC adapter
① Connect sphygmomanometer and the AC adapter. Insert the AC Adapter Plug into the
AC Adapter socket on the right side of the device.
② Please insert the power plug of AC adapter into the AC 100V～240V socket.
Note
When cut off the power, first cut off the connection of power socket and the regulated
power supply, then cut off the connection of regulated power supply and the
sphygmomanometer.
Please be sure to use dedicated AC adapter.
Note
When regulated power supply and dry batteries are both used at the same time, the dry
①
③
②
9
battery power will not be consumed.
Switch regulated power supply and dry batteries when the device is off, otherwise, the
device may shutdown due to power failure.
10
Chapter6 Button Functions
All the operations to the Electronic Sphygmomanometer are through buttons. The names of the
buttons are above them. They are:
【ON/OFF】 ON/OFF button. press it to turn on/off the device.
【START/STOP】Press to inflate the cuff and start a blood pressure
measurement. When measuring, press to cancel the measurement and deflate the cuff.
Long press this button can connect the network fleetly .
The three buttons correspond with the hint in the LCD screen
downside, pressing any button will carry on corresponding function, eg:【MENU】
【ENTER】【LIST】 etc.
Up and down buttons respectively carry on the functions of moving the cursor up
and down, chan
g
in
g
the
p
arameters and switchin
g
the status.
11
Chapter7 Set Date and Time
The Electronic Sphygmomanometer stores 100 groups of measurement results at most. If the date
and time are set correctly, the date and time when measuring will be correct in the memory,
otherwise it may not be correct.
Note
Correctly use data upload function:
1. First, make sure the time is right, there are three modes of time setting:
(1)When using the Sphygmomanometer for the first time or after the Sphygmomanometer
has been placed without power supply for a certain time(more than 5 minutes), after power on,
there is a prompt of time error on the main interface, set date and time with 【UP】, 【DOWN】
and 【ENTER】 button.
(2)Press 【MENU】 button on the main interface to enter system menu, then enter
【SYSTEM TIME】 item, the current time will be displayed on the screen. Set date and time
with 【UP】, 【DOWN】 and 【ENTER】 button
It is necessary to set date and time after power on.
The Electronic Sphygmomanometer can automatically stores
measurement results with date and time
If dry batteries power exhausts or removed, the time to stop.
At the moment, please reset date and time.
Short-term(less than 5 minutes) power cut does not affect time.(such as
replacing batteries)
12
(3)When the Sphygmomanometer is ON, users manually search and connect it through
mobile phone software, the time of the Sphygmomanometer will be synchronized.
2. After setting, select 【CONFIRM】 option and press 【ENTER】 button to confirm the
setting value. If you do not want to change the time, select 【EXIT】 option and press 【ENTER】
button to return to the previous menu.
13
Chapter8 Unit and Language
8.1 Measurement Unit
There are two units: "mmHg" and "kPa".
The default is "mmHg".
Enter 【SYSTEM SETUP】 submenu in 【MENU】, then select 【UNIT】 option to switch
units between "mmHg" and "kPa".
8.2 Language
The sphygmomanometer supports both English and Chinese, the default is Chinese, enter
【SYSTEM SETUP】 submenu in 【MENU】 and select 【LANGUAGE】 can switch
languages.
1
Chapter9 Alarm Function
Alarms are classified into two categories: technical alarm and physiological alarm.
9.1 Physiological Alarm
User can press 【MENU】 button to enter system menu, select 【ALARM SETUP】 option to
enter its interface, and then set alarm on-off and the high and low alarm limits, during setting
alarm parameter, if the high limit lower than the low limit, the device will display a prompt, users
allow or reset it according to the actual situation. When the measurement result is higher than the
high limit or lower than the low limit, the physiological alarm will occur.
Under physiological alarm, press any button to cancel this alarm, and it does not affect the next
alarm; the alarm can be closed permanently with alarm switch of the alarm setup menu until the
alarm switch be opened again.
9.2 Technical Alarm
When the battery is low and the alarm is on, the device will sound an alarm. This alarm can
not be cancelled, unless you turn off the alarm switch or replace the power supply.
2
Chapter10 Measurement Mode
The sphygmomanometer can be set to neonate, pediatrics and adult three modes.
Press 【MENU】button to enter 【SYSTEM SETUP】 interface, then users can set different
modes through 【USER TYPE】 option.
3
Chapter11 Application of the Sphygmomanometer
11.1 Accurate Measurement Way
11.2 Applying the Cuff
When measuring, take the thick clothes off instead of rolling up the sleeves.
In order to measure accurately, pay attention to applying the cuff properly (left arm).
① Insert the arm cuff air plug in the cuff socket of sphygmomanometer.
Measurement in quiet and relaxing state.
1.Place your elbow on a table.
2.The cuff is level with your heart.
3.The palm of the hand is up, and the body relax.
Try to measure your blood pressure at the same time each day with the same arm
and the same pose for consistency.
The high and low location of cuff will cause changes in measurement results.
Do not touch Electronic Sphygmomanometer, cuff and windpipe during measurement.
Measurements should be taken in a quiet place and the body relax.
Remain still 4~5 minutes before measurement.
Relax the body, do not let the muscle activity.
Do not talk and movement during the measurement.
Wait 4~5 minutes between measurements.
Please use the sphygmomanometer at an environment of suitable temperature and
humidit
y(
refer to Cha
p
ter20
)
, otherwise it will cause
m
easurement error.
The measurement can be carried out by applying the cuff on left or right arm.
Bare your arm or cloth close-fitting clothing during measurement.
Carry out the operation in a room with comfortable temperature.
4
② Stretch cuff into a barrel for the arm can conformable enter into the barrel.
③ Left arm penetrate through the cuff, the air tube of the cuff will pass the top of your palm.
④ Wrap the cuff to your upper arm. Make the air tube inside the forearm and aligned with your
middle finger.
⑤ The bottom of the cuff should be approximately 2cm~3cm above your elbow.
⑥ Be fixed with cloths, and wrapped tight cuff, the arm and the cuff should not have gaps.
11.3 BP Measurement
错误！未找到引用源。Press 【START/STOP】 button to take a measurement.
Start measurement Measurement result
5
During measurement, please keep correct pose and quiet state, do not move.
Wish to stop measurement
During measurement, press 【START/STOP】 button, stop press，release the air from the cuff.
错误！未找到引用源。Confirm the Measurement Value
The measurement value can be stored automatically, using [memory function] (refer to
Chapter12).
*Self-diagnosis and treatment using measured results may be dangerous. Follow the instructions
of your physician.
错误！未找到引用源。In no physiological alarm state, press any button to carry on the
corresponding button function; in audio alarm state, press any button (except 【ON/OFF】 button)
to clear up the audio alarm.
④Take off the cuff, press 【ON/OFF】 button to turn the device off.
*The device will automatically turn off after 1 minute in which there is no operation to the
device and no connection with SpO2 probe, even if you forget to turn the power off.
Note
Wait 4-5 minutes between measurements.
When repeated measurements, because, the arm appears congestion, it may not get correct
blood pressure measurement. After the blood flow, take a measurement once again.
When some factors affect the measurement results in measurement process, error
messages will appear on the screen, you can obviate the malfunction and restart a
measurement.
6
Chapter12 Memory Fuction
The devicer is designed to store and display the blood pressure, pulse rate values and the date and
time when measured, which are up to 100 groups. If there have been stored 100 groups, the
earliest results will be deleted when saving the 101 group of measurement results.
12.1 Read Memory Values
1. In the main interface (interface when boot-strap), press 【MEMORY】 button to review the
most recent measurement values in large-print, press 【LIST】 button to enter data list interface.
The device displays memory value with the number from 1 to 100. The little dot which is behind
serial number represent that the data has been uploaded or the data was measured at wrong
device time.
2. Press 【UP】/【DOWN】 button to circularly switch the former measurement values.
Press 【LIST】 button to enter the data list interface. The little dot which is before serial number
represent that the data has been uploaded or the data was measured at wrong device time.
3. Press 【TREND】 button to enter the trend graph interface.
*The right figure shows that there is no Measurement result
7
Finish displaying the measurement values.
Press 【EXIT】 button to return to the main interface or long press 【ON/OFF】 button to turn
the power off.
*The device will automatically turn off after 1 minute in which there is no operation to the
device and no connection with SpO2 probe, even if you forget to turn the power off.
12.2 Delete Memory Values
Users can delete all memory values of users instead of separately delete the special item.
1. Press 【MENU】 button to enter the system menu, select 【DELETE DATA】 to enter the
confirm interface, after confirming again, all measurement results will be deleted.
2. Finish Operation
Select 【CONFIRM】 or 【EXIT】 to return to the previous menu, or long press 【ON/OFF】
button to turn the power off.
*The device will automatically turn off after 1 minute in which there is no operation to the
device and not connect SpO2 probe , even if you forget to turn the power off.
8
Chapter13 Bluetooth Data Sending
The sphygmomanometer can send the storage BP value to PC through bluetooth.(refer to
software help for details)
Users connect the sphygmomanometer to PC after searching it on PC client, after completing the
connection, data will transmit to PC through bluetooth. After the sphygmomanometer finished
data transmission, it will mark in the measurement review interface. This mark is a green dot, it
on the right side of the top right corner serial number in memory interface; it on the left side of
left serial number in BP list interface. Note: when sphygmomanometer time error, the device
manage measurement data but does not upload it, now the dot in memory interface is red.
9
Chapter14 SpO2 Measurement Function
Precaution for SpO2 measurement
Note
◎Make sure the nail covers the light window. The wire should be on the backside of the hand.
SpO◎2 value is always displayed in the fixed place
◎The fingers which are too thin or too cold may affect the measure accuracy, please insert the
thicker finger such as thumb or middle finger deeply enough into the probe.
◎The SpO2 probe is suitable for children above four years old and adults(Weight should be
between 15Kg to 110Kg). The device may not work for all patients. If you are unable to achieve
stable readings, discontinue use it. Do not use the device on infant or neonatal patients.
The update period of data is less than 5 seconds, which is changeable according to different ◎
pulse rate values.
◎Pulse rate waveform through the normalization, when pulse rate waveform becomes smooth
and stable, the read value is optimal value, and the waveform at the moment is the most standard
one.
◎The maximum temperature for the contact surface of the device with the body is less than
41 , and the tempera℃ture is measured by a temperature measuring device.
The◎ SpO2 probe does not have an alarm function.
The◎ SpO2 probe has been calibrated before leaving factory.
Warning
◎Please don't measure this device with function tester for the device's related information.
◎The person who is allergic to rubber can not use this device.
◎Check if the cable of SpO2 probe is in normal condition before monitoring. After unplugging
the SpO2 probe cable from the socket, SpO2% and bmp on the screen will disappear.
◎Do not use the SpO2 probe once the package or the probe is found damaged. Instead, you shall
return it to the vendor.
T◎he uncomfortable or painful feeling may appear if using the device ceaselessly, especially for
Warning
◎Pulse oximeter can overestimate the SpO2 value in the presence of Hb-CO,
Met-Hb or dye dilution chemicals.
◎ES (Electrosurgery) equipment wire and SpO2 cable must not be tangled up.
◎Do not put the sensor on extremities with arterial catheter or venous syringe.
◎Do not perform SpO2 measuring and NIBP measuring on the same arm at one
time, because obstruction of blood flow during NIBP measuring may adversely affect
10
the microcirculation barrier patients. It is recommended that the sensor should not be applied to
the same finger for over 2 hours.
◎Prolonged and continuous monitoring may increase jeopardy of unexpected change of dermal
condition such as abnormal sensitivity, erubescence, vesicle, repressive putrescence, Particularly
in newborns or in a Perfusion disorders and changes or immature skin form of the patient.
According to skin quality change, correct optical path alignment and attachment methods to
regularly check the place of SpO2 probe, and change the attachment position when the quality of
skin decline. More frequent examinations may be required for different patients.
11
Chapter15 SpO2 Measurement Method
1. Attach the sensor to the appropriate site of the patient finger as following figure.
2. Plug the connector of the SpO2 probe cable into the USB socket in the lower right of the
device. The main interface will switch to SpO2 interface. This operation brings no affection to
other functions.
Measurement Limitation
During operation, the accuracy of oximeter readings can be affected by:
High-frequency electromagnetic interference such as electrosurgical apparatus connected to
the system;
Intravenous dyestuff;
Excessive patient movement;
Outside ray radiation;
Improper SpO2 probe installation or incorrect contact position of the patient;
SpO2 probe temperature (optimal temperature between 28°C and 40°C)
Place the SpO2 probe on an limb that has a blood pressure cuff, arterial catheter, or
intravascular line.
Concentrations of dysfunctional hemoglobin, such as carboxyhemoglobin(COHb) and
methemoglobin(MetHb);
SpO2 is too low;
Bad circular injection of the part being measured;
It is required to use SpO2 probe which is provided by our company, contact with our sale
department when changes SpO2 probe.
Place SpO2 probe
12
Chapter16 Maintenance, Cleaning and Keeping
*Please follow the instructions in the user manual. If you do not comply, our company will
not assume responsibilities of the quality.
Warning
Must remove batteries and cut off the alternating power supply before cleaning the
sphygmomanometer, accessories must be clean separately.
Caution
Do not high pressure disinfect the sphygmomanometer and accessories.
Do not immerse the sphygmomanometer and accessories into any liquid.
Do not use any sphygmomanometer and accessories that may be damaged or deteriorated.
Cleaning:
If there is something dirty on the sphygmomanometer and accessories, please wipe it with a
dry and soft cloth.
If the sphygmomanometer and accessories are very dirty, you can clean them with a soft
cloth dampened with water or neutral detergent after the cloth can be full twisted.
Maintenance:
Advice
Do not use any naphtha, thinner or gas to clean.
Do not attempt to clean or wash the cuff.
Frequently clean the Sphygmomanometer and accessories.
The device should be calibrated regularly( or according to
the calibration procedure of hospital). Users can go to the
inspection agency designated by the state to calibrate it, or
compared with the standard pressure gauge, at any measuring
point, the maximal error of measuring the pressure in cuff
should be ±0.4kPa(±3mmHg); also can contact with our
company.
13
Keeping:
Advice
Note
The service life of the device is five years. When the product and accessories described in this
manual are about to exceed the period of use, they must be disposed according to relevant
product handling specification. If you want to know more information, please contact our
company or representative organization
Do not place the device in the following areas:
Easy to splash water areas.
Direct sunlight, extreme hot, humidity, dust, causticity gas areas.
Lean or the area which can cause vibration, impact.
Chemicals or corrosive gas storage areas.
Remove the batteries if the device will not be used for long time.
14
Chapter17 Error Message
Error message will be displayed in the screen if there is something wrong when measuring. The
causes and solutions are shown as follows:
Error message Causes Solutions
Self-test failure
System error
Function abnormal Please contact us
Loose cuff Cuff is not connected correctly Correctly connect cuff(refer to chapter11)
Air leakage Cuff plug fall off
Inserted the cuff plug in the windpipe
correctly(refer to chapter11)
Air pressure error Air pressure error Keep arm, body still, measure again
Weak signal
The pulse is too weak or the cuff
is loose
Correctly connect cuff(refer to chapter11)
overpressure Cuff is blocked or squeezed Correctly connect cuff(refer to chapter11)
Excessive
movement
Over range
Saturated signal
The signal extent is too big
owing to the arm or body
moving or other reasons when
measuring Keep arm, body still, measure again
Time out It takes too much time
15
Chapter18 Troubleshooting
Abnormal Phenomenons Causes Solutions
BP measurement values
too high or too low
Cuff is not connected correctly Correctly connect cuff(refer to
chapter11)
Talk or move arms when measuring Keep quiet and restart a
measurement
The turnup clothing presses the arm Take off the clothing which presses
the arm, and restart a measurement
No pressure
Cuff leakage Buy a new cuff
The cuff windpipe is not correctly
connected with cuff Correctly connect
Cuff deflates in short
time Loose cuff Correctly connect
It can not carry on measurement when press the measurement
button
Switch on the power once again
and restart a measurement
Power off suddenly when
inflating
No use for a long time, the power
of batteries can be exhausted
owing to the changed temperature
Charge batteries
Display nothing after hold
the ON/OFF button
Power of batteries can be
exhausted Charge batteries
The battery polarities is reversed Correctly put in batteries
Other phenomenon
Please hold the on/off button and
restart an operation.
Please charge batteries
If no, please contact us.
16
Chapter19 Meanings of Symbols
Symbol Description
Warning – refer to User Manual
Refer to the accompanying document(the User Manual)
SYS Systolic pressure
MAP Mean pressure
DIA Diastolic pressure
PR Pulse rate (bpm)
ADU Adult
INFO Information
The alarm is ON
The alarm is OFF
Low-power
Full-power
1.no finger inserted to SpO2 probe
2.An indicator of signal inadequacy
Class equipmentⅡ
WEEE (2002/96/EC)
T
yp
e BF A
pp
lied Part
SN Serial number
This item is compliant with Medical Device Directive 93/42/EEC of June
14, 1993, a directive of the European Economic Community.
European Representative
USB socket connect SpO2 probe(this item only applies to EU market)
17
Chapter20 Specification
Name Electronic Sphygmomanometer
The degree of
protection against
ingress of liquid
Ordinary sealing device, without the function of preventing liquid from
entering
Display mode 2.8"color LCD Display
NIBP Specifications
Measurement Method Oscillometric method
Working mode Manual operation
Measurement Range Pressure
adult 0~290mmHg(0~38.6kPa)
pediatric 0~235mmHg(0~31.3kPa)
neonatal 0~140mmHg(0~18.6kPa)
Pulse: 40~240/min
Inflation
adult 160mmHg
pediatric 120mmHg
neonatal 70mmHg
Overpressure protect
adult mode 295±5mmHg
pediatric mode 240±5mmHg
neonatal mode 145±5mmHg
Resolution Pressure: 1mmHg(0.133kPa)
Accuracy Static pressure: ±3mmHg(±0.4kPa)
Error
The BP Value of the device is equivalence with the measurement value
of Stethoscopy. The error meets all the conditions in the ANSI/AAMI
SP-10:2002+A1:2003 +A2:2006.
Operating Temperature/
Humidity +5ºC～40 ºC 15%RH～80%RH
Transport Transport by general vehicle or according to the order contract, avoid
pounded, shake and splash by rain and snow in transportation.
Storage Temperature: -20ºC～+55ºC; Relative humidity: ≤95%; No corrosive
gas and drafty.
Atmospheric pressure 700hPa～1060hPa
Battery 4 "AA" alkaline batteries, AC Adapter(AC, 100V-240V, optional)
Dimensions 130(L)*110(W)*80mm(H)
Unit Weight 300g(not including batteries)
18
Safety classification class Ⅱ, type BF applied equipment
Service life The service life of the device is five years or 10000 times of BP
measurement.
FCC Cautions:
1) This device complies with part 15 of the FCC Rules. Operation is subject to
the following two conditions: (1) This device may not cause harmful interference, and
(2) this device must accept any interference received, including interference that may
cause undesired operation.
2) Note: This equipment has been tested and found to comply with the limits for a Class B
digital device, pursuant to part 15 of the FCC Rules. These limits are designed to
provide reasonable protection against harmful interference in a residential installation.
This equipment generates uses and can radiate radio frequency energy and, if not
installed and used in accordance with the instructions, may cause harmful interference
to radio communications. However, there is no guarantee that interference will not
occur in a particular installation. If this equipment does cause harmful interference to
radio or television reception, which can be determined by turning the equipment off and
on, the user is encouraged to try to correct the interference by one or more of the
following measures:
-Reorient or relocate the receiving antenna.
-Increase the separation between the equipment and receiver.
-Connect the equipment into an outlet on a circuit different from that to which the
receiver is connected.
-Consult the dealer or an experienced radio/TV technician for help.
3) Any Changes or modifications not expressly approved by the party
responsible for compliance could void the user's authority to operate the equipment.
The device has been evaluated to meet general RF exposure requirement. The device can be used
in portable exposure condition without restriction.