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- 12 - 05/2020
Copyright © 2020, Fast ČR, a.s.
This device meets the requirements of European Directive No.
93/42/EEC.
Manufacturer: Guangdong Transtek Medical Electronics Co.,
Ltd., Zone A, No.105 , Dongli Road, Torch Development District,
Zhongshan, 528437, Guangdong, China
SN
This symbol indicates the serial number.
This symbol indicates direct electrical current.
This symbol indicates the date of manufacture, which is provided
on the rating label.
This symbol indicates the BF type applied parts.
EC REP This symbol indicates an authorised representative for the EU:
MDSS - Medical Device Safety Service GmbH, Address: Schiffgraben
41, 30175 Hannover, Germany
This symbol indicates that the device is intended for recycling.
The Green Dot symbol is the license symbol of aEuropean network
of industry-funded systems for recycling the packaging materials
of consumer goods.
TROUBLESHOOTING
In this chapter you will find solutions to problems that you may encounter when
using this device. If you were unable to remedy the problem according to the
following instructions, contact an authorised service centre.
PROBLEM CAUSE SOLUTION
After pressing the
START/STOP A5
button, the display A6
does not turn on.
The batteries are probably
flat.
Replace the batteries with
new ones.
The batteries are inserted
incorrectly.
Insert the batteries according
to the markings on the bottom
of the battery compartment.
The symbol and
the message "LO"
will appear on the
display A6.
The batteries are flat. Replace the batteries with
new ones.
Error message E 01
appeared on the
display A6.
The cuff is fastened too
tightly or too loosely.
Unfasten the cuff, adjust the
setting and refasten it. Repeat
the measurement.
Error message E 02
appeared on the
display A6.
The device registered an
arm / body movement
during measurement.
Movement may affect the
measurement correctness.
Relax for afew moments and
then repeat the measurement.
Error message E 03
appeared on the
display A6.
The device did not
register apulse during
measurement.
Loosen arolled up sleeve,
or alternatively take off your
jumper or tracksuit top that
you are wearing. Repeat the
measurement.
Error message E 04
appeared on the
display A6.
Measurement failed. Relax for afew moments and
then repeat the measurement.
Error message EExx
appeared on the
display A6.
Acalibration error occurred
(as arule, xx is anumber,
e.g. 01, 02, etc., all values
relate to calibration error
during calibration).
Repeat the measurement. If
the problem persists, please
contact an authorised service
centre.
Error message "out"
appeared on the
display A6.
The measured values are
outside the range of the
device.
Relax for awhile. Put the
cuff back on and repeat the
measurement. If the problem
persists, please contact your
doctor.
TECHNICAL SPECIFICATIONS
Power supply 4x type AAA batteries (included)
Display Blue LCD with awhite backlight, dimensions:
65×50mm
Measuring method Oscillometric
Measuring range Cuff pressure: 0mmHg – 299mmHg
Measured pressure
SYS: 60mmHg – 230mmHg
DIA: 40mmHg – 130mmHg
Pulse: 40 – 199 pulses / minute
Measurement accuracy Pressure: ± 3mmHg (0.4 kPa) at atemperature of
5 – 40°C
Pulse: ± 5%
Standard operational
conditions
Operating temperature range: 5 – 40°C
Relative humidity range: 15 – 90% (non-
condensating environment, however without water
vapour)
Partial pressure greater than 50 hPa
Atmospheric pressure range: 700 hPa – 1060 hPa
Storage and transportation
conditions
Temperature: -20°C - + 60°C
Relative humidity range ≤ 93% (non-condensating
environment)
At awater vapour pressure of up to 50 hPa
Adjustable length of
the cuff
22 – 42cm
Weight Approx. 225 g (without batteries and cuff)
External dimensions 120.2×108.2×68.5mm
Accessories Cuff, 4x AAA type batteries, user'smanual
Operating mode Continuous operation
Protection level Type BF applied part
Protection against the
effect of water
IP21 (means that the device is protected against
solid foreign objects of size 12.5mm and larger and
against water drops falling vertically on the device)
Device classification The device is only battery-powered.
Internally-powered medical electrical device
Power adapter power supply mode: class II medical
electrical device.
Software version A04
We reserve the right to change text and technical specifications.
12


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