INTRODUCTION................................................................................................................
Safety Information
LCD Display Signal
Monitor Components
BEFORE YOU START.......................................................................................................
The Choice of Power Source
Install App and Pair-Up
Settings
START MEASUREMENT...................................................................................................
Apply the Cuff
Start Measurement
DATA MANAGEMENT.......................................................................................................
Recall the Records
Delete the Records
Data Transmission
INFORMATION FOR USER...............................................................................................
Tips for measurement
Maintenance
ABOUT BLOOD PRESSURE ............................................................................................
What are systolic pressure and diastolic pressure?
What is the standard blood pressure classification?
Why does my blood pressure fluctuate throughout the day?
Why the blood pressure I get from the hospital is different from
home?
The result is different that you measuring on the different arm.
TROUBLESHOOTING.......................................................................................................
SPECIFICATIONS..............................................................................................................
AUTHORIZED COPMONENT............................................................................................
COMPLIED EUROPEAN STANDARDS LIST....................................................................
ELECTROMAGNETIC COMPATIBILITY DESCRIPTIONS................................................
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4
8
10
12
14
12
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14
14
15
CATALOGUE INTRODUCTION
1
The below signs might be in the user manual, labeling or other component.
they are the requirement of standard and using.
Safety information
T1A/250V Φ3.6*10CCC
EC REP
F1
Thank you for selecting TRANSTEK arm type blood pressure Monitor (LS805-B).
The monitor features blood pressure measurement, pulse rate measurement and
auto-save the result. The design provides you with two years of reliable service.
Reading taken by the LS805-B 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:
For indoor use only
128mm x 50mm Blue LCD display with white backlight
Up to 60 pieces of record stored for each user
Measure-during-inflating Technology
Symbol for “COMPLIES WITH
MDD93/42/EEC
REQUIREMENTS”
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 “Authorised Representative in the European Community”
Symbol for “Class II Equipment”
This device is intended for adult use in the home/domestic only.
This device is intended for non-invasive measuring and monitoring of arterial blood pressure. It is not
intended for use on extremities other than the upper 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. Please start or end medical treatment basing solely on physician’s treatment advice.
If you are taking medication, consult your physician to determine the most appropriate time for your
measurement. Never change a prescribed medication without your physician’s consent.
This unit is not suitable for continuous monitoring during medical emergencies or operations.
If the pressure of the cuff exceeds 40 kPa (300 mmHg), the unit will automatically deflate. Should the
cuff not deflate when its pressure exceeds 40 kPa (300 mmHg), detach the cuff from the upper arm
and press the homologous button to stop inflation.
Please do read this user manual carefully and thoroughly before use.
The device is not AP/APG equipment. It is not suitable for use in the presence of a flammable
anesthetic mixture with air (or oxygen, nitrous oxide).
Do not touch the output of AC adapter and the patient simultaneously.
Do not use the monitor under the conditions of strong electromagnetic field (e.g. mobile) that radiates
interference signal or electrical fast transient / burst signal, especially when the AC adaptor is applied.
Please keep the unit out of reach of infants or children, since inhalation or swallowing of small parts
is dangerous or even fatal.
CAUTION
Please use ACCESSORIES and detachable parts specified / authorised by MANUFACTURER.
Otherwise, it may cause damage to the unit or danger to the user / patient.
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 alergic reaction or contact injury.
Please make sure the unit functions safely and it is in proper working conditions before use.
The Bluetooth Combination Mark
Symbol for “THE OPERATION
GUIDE MUST BE READ”