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Bernafon CROS miniRITE T R Notice D'utilisation page 47

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The manufacturer declares that this
transmitter is in compliance with the es-
sential requirements and other relevant
provisions of Directive 2014/53/EU.
Declaration of Conformity is available at
the headquarters website
www.bernafon.ca/doc.
This medical device complies with
Medical Device Regulation (EU)
2017/745.
SBO Hearing A/S
Denmark
Declaration of Conformity is available at
the headquarters.
Bernafon AG
Morgenstrasse 131
3018 Bern
Switzerland
www.bernafon.ca/doc
Waste from electronic
equipment must be
handled according to
local regulations.
47

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