Instructions For Use - Sanitas SBM 37 Instructions For Use Manual

mobile HF communication systems may interfere with this
unit. More details can be requested from the stated Custom-
er Services address or found at the end of the instructions
for use.
• The device complies with the EU Medical Devices Directive
93/42/EC, the German Medical Devices Act (Medizinproduk-
tgesetz) and the standards EN1060-1 (non-invasive sphyg-
momanometers – Part 1: General requirements), EN1060-3
(non-invasive sphygmomanometers – Part 3: Supplementary
requirements for electro-mechanical blood pressure measur-
ing systems) and IEC80601-2-30 (Medical electrical equip-
ment – 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 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.
Precise instructions for checking accuracy may be requested
from the service address.
• We hereby guarantee that this product complies with the
European R&TTE Directive 1999/5/EC.
Please contact the specified service address to obtain more
detailed information such as the CE conformity declaration.
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