54 55
Indicates the date when the medical device
was manufactured.
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 these user guides.
This symbol indicates that it is important
for the user to pay attention to the relevant
warning notices in these user guides.
This symbol indicates that it is important for
the user to pay attention to the relevant
warning notices related to batteries in these
user guides.
22. Information and description
of symbols
With the CE symbol, Sonova AG conrms
that this product – including accessories –
meets the requirements of the Medical
Devices Regulation (EU) 2017/745 as well as
the Radio Equipment Directive 2014/53/EU.
The numbers after the CE symbol correspond
to the code of certied institutions that were
consulted under the above-mentioned
regulation and directive.
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 hearing
aid is specied as an applied part of Type B.
Indicates the medical device manufacturer, as
dened in Medical Device Regulation (EU)
2017/745.