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21. Information and description
ofsymbols
With the CE symbol, Sonova AG conrms
that this product – including accessories –
meets the requirements of the Medical
Devices Regulation 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
directives.
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,
asdened in EU Directive 93/42/EEC
Indicates the date when the medical device
was manufactured