Bedienungsanleitung Sencor SBP 6800 (Seite 12 von 13) (Englisch)

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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

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

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.

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