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9. Information and description
of symbols
With the CE symbol, Sonova AG conrms that
this product meets the requirements of the EU
Medical Device Regulation 2017/745.
Indicates the medical device manufacturer,
as dened in EU Medical Device Regulation
2017/745.
Indicates the Authorized representative in the
European Community. The EC REP is also the
importer to the European Union.
This symbol indicates that it is important for the
user to read and take into account the relevant
information in this user guide.
This symbol confers that the electromagnetic
interference from the device is under limits
approved by the US Federal Communications
Commission