oticon CROS PX miniRITE R Instructions For Use Manual page 47

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.oticon.global/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.
Oticon A/S
Kongebakken 9
DK-2765 Smørum
Denmark
www.oticon.global/doc
Waste from electronic
equipment must be
handled according to
local regulations.
47