Beurer BC 40 - Manual (Page 26)

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Technical information is subject to change without notifica-
tion to allow for updates.
• This device is in line with European Standard EN 60601-1-2
and is subject to particular precautions with regard to elec-
tromagnetic 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 Direc-
tive 93/42/EC, the German Medical Devices Act (Medizin-
produktgesetz) and the standards EN 1060-1 (non-inva-
sive sphygmomanometers, Part 1: General requirements),
EN 1060-3 (non-invasive sphygmomanometers, Part3:
Supplementary requirements for electro-mechanical blood
pressure measuring systems) and IEC80601-2-30 (Medical
electrical equipment – Part 2 – 30: Particular requirements
for the basic safety and essential performance of auto-
mated 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 pur-
poses, it must be regularly tested for accuracy by appro-
priate means. Precise instructions for checking accuracy
may be requested from the service address.