Silvercrest 366722 2101 Gebrauchsanleitung Und Sicherheitshinweise Seite 42

This device complies with European Standard EN 60601-1-2
(in accordance with CISPR 11, IEC 61000-4-2, IEC 61000-4-3,
IEC 61000-4-8) and is subject to special precautions with
respect to electromagnetic compatibility. The device is suitable
for use in all environments listed in these instructions for use,
including domestic environments. Please note, portable and
mobile HF communication devices may interfere with this
device. This device complies with EU Medical DevicesDirective
93/42/EEC, the Medical Devices Act and standard IEC
80601-2-30 (Medical electrical equipment Part 2-30: Par-
ticular requirements for basic safety and essential perfor-
mance of automated non-invasive blood pressure monitors).
The accuracy of this blood pressure monitor has been
thoroughly tested and was developed with regard to a long
utilizable service life. If the device is used in medicine, tech-
nical inspections using the suitable equipment are to be car-
ried out. Precise information on how to test the accuracy of
the device can be requested from our service address.
We hereby affirm that this product complies with the
European RED Directive 2014/53/EU.
The CE declaration of conformity for this product is
available at:
www.sanitas-online.de/web/de/landingpages/
cedeclarationofconformity.php
42 GB/IE/NI