Bernafon Acriva, Инструкция по эксплуатации

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39
Compliance with Requirements
for Europe
All devices covered in these instructions for use
are in conformance with the requirements of the
Directive 93/42/EEC of the Council of the European
Communities concerning medical devices, MDD.
This is certified by applying the following marking:
All devices with wireless functionality (Juna, Acriva,
Chronos, Carista, and Saphira families) also comply
with the essential requirements of the Directive
1999/5/EC of the European Parliament on radio
equipment and telecommunications terminal equip-
ment, R&TTE. It operates as an inductive application
in a harmonized frequency band according to the
Commission Decision 2008/432/EC and may be
used in all member states of the EU and EFTA. This
is certified by applying the following marking:
Declaration of conformity is available at:
Bernafon AG
Morgenstrasse 131
3018 Bern
Switzerland