Sanitas SBC 53 Mode D'emploi page 36

Technical information is subject to change without notification
to allow for updates.
• This device complies with European Standard EN60601-
1-2 and is subject to particular precautions with regard to
electromagnetic compatibility. Please note that portable and
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/EEC, the German Medical Devices Act (Medizinpro-
duktgesetz) and the standards EN1060-1 (non-invasive
sphygmomanometers – Part 1: General requirements),
EN1060-3 (non-invasive sphygmomanometers – Part 3:
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 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 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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