Phonak Audeo M-R Series, Руководство пользователя

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8. Information and description
of symbols
With the CE symbol, Sonova AG confirms that
this product meets the requirements of the
Medical Regulation 2017/745.
This symbol indicates that the products
described in these user instructions adhere to
the requirements for an applied part of Type B
of EN 60601-1. The surface of the device is
specified as an applied part of Type B.
Indicates the medical device manufacturer,
as defined 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.