Beurer BC 57, Instructions For Use Manual

Page: 36 / 152

36
Permissible operating
conditions
+10 °C to +40 °C, ≤ 85 % relative
humidity (non-condensing)
Permissible storage
conditions
-20 °C to +50 °C, ≤ 85 % relative
humidity, 800-1050 hPa ambient
pressure
Power supply 2 x 1.5V AAA batteries
Battery life For approx. 200 measurements, de-
pending on levels of blood pressure
and pump pressure
Data transfer 2402 MHz – 2480 MHz frequency
band
Transmission power max. 2.8 dBM
The blood pressure monitor uses Blue-
tooth ® low energy technology
Compatible with Bluetooth ® 4.0
smartphones/tablets
List of supported smartphones/tab-
lets
The serial number is located on the device or in the bat-
tery compartment.
Technical information is subject to change without notifi-
cation to allow for updates.
š This device is in line with European Standard EN
60601-1-2 (In accordance with CISPR 11, IEC 61000-
4-2, IEC 61000-4-3 and IEC 61000-4-8) and is subject
to particular precautions with regard to electromagnetic
compatibility (EMC). Please note that portable and mo-
bile HF communication systems may interfere with this
unit.
š This device corresponds to the EU Medical Devices
Directive 93/42/EEC, the German Medical Devices Act
(Medizinproduktgesetz) and the standards EN 1060-1
(non-invasive sphygmomanometers, Part 1: General
requirements), EN 1060-3 (non-invasive sphygmoma-
nometers, Part3: Supplementary requirements for
electro-mechanical blood pressure measuring systems)
and IEC 80601-2-30 (Medical electrical equipment –
Part 2-30: Particular requirements for the basic safety
and essential performance of automated non-invasive
sphygmomanometers).
š The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life.
š If using the device for commercial medical purposes,
it must be regularly tested for accuracy by appropriate
means. Precise instructions for checking accuracy may
be requested from the service address.
š We hereby confirm that this product complies with the
European RED Directive 2014/53/EU. The CE Declara-
tion of Conformity for this product can be found under:
www.beurer.com/web/we-landingpages/de/cedeclara-
tionofconformity.php.