TRANSTEK LS802-E User Manual
User Manual
Blood Pressure Monitor
LS802-E
To use the monitor correctly and safely, please read the manual
thoroughly.
Thank you very much for selecting TRANSTEK Blood Pressure Monitor
LS802-E.
please keep well this manual in order to reference in future.
Arm Type
Version:1.0
FCC ID:OU9LS802-E02
GUANGDONG TRANSTEK MEDICAL ELECTRONICS CO.,LTD
Zone A, 5/F., Investment Building, No. 12, Huizhan East Rd., Torch
Development District, Zhongshan, Guangdong, 528437, China
CATALOGUE
1
Table of Contents
CATALOGUE
INTRODUCTION..............................................................................................................................2
General Description
Safety Information
LCD Display Signal
Monitor Components
BEFORE YOU START......................................................................................................................6
The Choice of Power Supply
Installing and Replacing the Batteries
MEASUREMENT..............................................................................................................................8
Tie the Cuff
Start the Measurement
INFORMATION FOR USER...........................................................................................................10
Tips for measurement
Maintenances
ABOUT BLOOD PRESSURE.........................................................................................................12
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why my blood pressure is varies even in one day?
Why the blood pressure I get from the hospital is different from home?
If the result is the same if measuring on the right arm?
TROUBLESHOOTING ...................................................................................................................14
SPECIFICATIONS..........................................................................................................................15
AUTHORIZED COMPONENTS ....................................................................................................16
CONTACT INFORMATION.............................................................................................................16
FCC STATEMENT...........................................................................................................................17
COMPLIED STANDARDS LIST.....................................................................................................18
EMC GUIDANCE............................................................................................................................19
The below signs might be in the user manual, labeling or other component.
they are the requirement of standard and using.
Safety Information
INTRODUCTION INTRODUCTION
2 3
Thank you for selecting TRANSTEK arm type blood pressure Monitor (LS802-E).
The monitor features blood pressure measurement, pulse rate measurement and the
the result storage. The design provides you with two years of reliable service.
Reading taken by the LS802-E are equivalent to those obtained by a trained
observer using the cuff and stethoscope auscultation method.
This manual contains important safety and care information, and provides step
by step instruction for using the product.
Read the manual thoroughly before using the product.
Features:
92*78mm Blue LCD display with white backlight
Maximum 60 records per each user
Measuring during inflation technology
General Description
T1A/250V Φ3.6*10CCC
F1
For indoor use only
Symbol for “MANUFACTURER”
Symbol for “SERIAL NUMBER”
Symbol for “TYPE BF APPLIED
PARTS”
Symbol for “ENVIRONMENT
PROTECTION – Waste electrical
products should not be disposed of
with household waste. Please follow
local guidelines.”
Symbol for “DIRECT CURRENT”
Symbol for “Class II Equipment”
Symbol for “THE OPERATION
GUIDE MUST BE READ”
Symbol for “MANUFACTURE
DATE”
This device is intended for adult use only.
This device is intended for no-invasive measuring and monitoring of arterial blood pressure.
It is not intended for use on extremities other than the arm or for functions other than obtaining a
blood pressure measurement.
Do not confuse self-monitoring with self-diagnosis. This unit allows you to monitor your blood
pressure.Do not begin or end medical treatment based solely physician for treatment advice.
If you are taking medication,consult your physician to determine the most appropriate time to
measure your blood pressure. Never change a prescribed medication without consulting your
Physician.
When the device was used to measure patients who have common arrhythmias such as atrial or
ventricular premature beats or artrial fibrillation, the best result may occure deviation. Please
consult your physician about the result.
If the cuff pressure exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the
cuff not deflate when pressures exceeds 40 kPa (300 mmHg), detach the cuff from the armand
press the START/STOP button to stop inflation.
The equipment is not AP/APG equipment and not suitable for use in the presence of a flammable
anesthetic mixture with air of with oxygen or nitrous oxide.
The operator shall not touch output of batteries /adapter and the patient simultaneously.
To avoid measurement errors, please avoid the condition of strong electromagnetic field radiated
interference signal or electrical fast transient/burst signal.
The user must check that the equipment functions safely and see that it is in proper working
condition before being used.
This device is contraindicated for any female who may be suspected of, or is pregnant. Besides
provided inaccurate readings, the affects of this device on the fetus are unknown.
Manufacturer will make available on request circuit diagrams, component parts list etc.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
Otherwise, the patient’s arm and fingers will become anaesthetic, swollen and even purple due to
a lack of blood.
Please use the device under the environment which was provided in the user manual. Otherwise,
the performance and lifetime of the device will been impacted and reduced.
During using, the patient will contact with the cuff. The materials of the cuff have been tested and
found to comply with requirements of ISO 10993-5:2009 and ISO 10993-10:2010. It will not
cause any potential sensization or irritation reaction.
Please use ACCESSORIES and detachable partes specified/ authorised by MANUFACTURE.
Otherwise, it may cause damage to the unit or danger to the user/patients.
The device doesn’t need to be calibrated in two years of reliable service.
Please dispose of ACCESSORIES, detachable parts, and the ME EQUIPMENT according to the
local guidelines.
If you have any problems with this device, such as setting up, maintaining or using, please
contact with SERVICE PERSONNEL of Transtek. Don’t open or repair the device by yourself.
Please report to Transtek if any unexpected operation or events occur.
Please use the soft cloth to clean the whole unit. Don’t use any abrasive or volatile cleaners.
The device has been evaluated clinically used manual cuff/stethoscope ausculation as the
reference. Blood pressure measurements determined with this device are equivalent to those
obtained by a trained observer using the cuff/stethoscope auscultatory method, within the limits
prescribed by the American National Standard, Manual, electronic, or automated
sphygmomanometers.”
CAUTION
Wireless Transmission
CUFF
AIR PIPE
AIR CONNECTOR PLUG
LCD DISPLAY
DC POWER SOCKET
User 1
Guest
User 2
BATTERY COMPARTMENT
Monitor Components
LCD Display Signal
5
4
List
1.Blood Pressure Monitor
(LS802-E)
4.User manual3. 4*AA alkaline batteries
2.Cuff (Type BF applied part)
SYMBOL DESCRIPTION
Systolic blood pressure High pressure result
Diastolic blood pressure Low pressure result
EXPLANATION
Pulse Pulse/minute
User 1 Provide measurement for user 1, and
then save the measure data
Guest
Provide measurement for guests,
but not save the measurement data.
User 2
Provide measurement for user 2, and
then save the measure data
Data storage
To remind the users that the measurement
data don’t upload to bridge in time
Wireless transmitter
The blood monitor and Bridge in communication
Network connection The bridge not connect the network
Shocking remainding Shocking will result in inaccurate
Low battery Batteries are low and need to be replaced
Measurement Unit of the blood pressure
Unit
date (hour:minute) Currently time
Deflating
CUFF air is exhausting of deflating
Component list of
pressure measuring system
1 Cuff
2 Air pipe
3 PCBA
4 Pump
5 Valve
Arrhythmia Irregular heartbeat
Heartbeat Heartbeat detection during the measurement
INTRODUCTION
INTRODUCTION
(22~32cm or 22cm~42cm)
5. AC Adaptor
(UE08WCP-060100SPA only!)
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