Beurer BC 57 Instrucciones De Uso página 35

The serial number is located on the device or in the bat-
tery compartment.
• This device is in line with European Standard EN
60601-1-2 and is subject to particular precautions with
regard to electromagnetic compatibility (EMC). Please
note that portable and mobile HF communication sys-
tems may interfere with this unit. More details can be
requested from the stated Customer Services address
or found at the end of the instructions for use.
• 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).
• The accuracy of this blood pressure monitor has been
carefully checked and developed with regard to a long
useful life.
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.
• We hereby guarantee that this product complies with
the European RED Directive 2014/53/EU. Please con-
tact kd@beurer.de to obtain detailed information, such
as the CE Declaration of Conformity.
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