47
Waste from electronic
equipment must be
handled according to
local regulations.
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.
Declaration of Conformity is available at
the headquarters.
Oticon A/S
Kongebakken 9
DK-2765 Smørum
Denmark
www.oticon.global/doc
SBO Hearing A/S
Denmark
Summary of Contents for CROS PX miniRITE R
Page 1: ...Instructions for use Oticon CROS PX miniRITE R...
Page 9: ...9 Hearing aid Transmitter Sound transmission...
Page 13: ......