Bernafon ACRIVA 9 - Compliance with Requirements for Europe

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Compliance with Requirements

for Europe

This device is in conformance with the require-

ments of the Directive 93/42/EEC of the Council

of the European Communities concerning medical

devices, MDD. This is certied by applying the

following marking:

This device also complies with the essential

requirements of the Directive 1999/5/EC of the

European Parliament on radio equipment and

telecommunications terminal equipment, 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 certied by applying the following marking:

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