Beurer BC 50 Instrucciones De Uso página 24

Classification Internal supply, IPX0, no AP or APG,
continuous operation, application part
type BF
• This device is in line with European Standard EN 60601-1-2
and is subject to particular precautions with regard to electro-
magnetic compatibility (EMC). Please note that portable and
mobile HF communication systems 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/EC, the German Medical Devices Act (Medizinproduk-
tgesetz) and the standards EN 1060-1 (non-invasive sphyg-
momanometers, Part 1: General requirements), EN 1060-3
(non-invasive sphygmomanometers, Part3: Supplementary
requirements for electro-mechanical blood pressure measur-
ing systems) and IEC 80601-2-30 (Medical electrical equip-
ment – Part 2-30: Particular requirements for the basic safety
and essential performance of automated non-invasive sphyg-
momanometers).
• The accuracy of this blood pressure monitor has been care-
fully 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. Pre-
cise instructions for checking accuracy may be requested
from the service address.
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