oticon ConnectLine Streamer Pro 1.3A, Инструкция по эксплуатации

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68 69 About Start-up Handling Functions Warnings More info
The manufacturer declares that this device is
in compliance with the essential requirements
and other relevant provisions of Directive
2014/53/EU.
This medical device complies with Medical
Device Regulation (EU) 2017/745.
Declaration of conformity is available at the
manufacturer.
Oticon A/S
Kongebakken 9
DK-2765 Smørum
Denmark
www.oticon.global
Waste from electronic
equipment must be
handled according to
local regulations.
Operation is subject to the following two
conditions:
1. this device may not cause harmful
interference, and
2. this device must accept any interference
received, including interference that may
cause undesired operation.
Note
Changes or modifications not expressly
approved by the party responsible for
compliance could void the user’s authority to
operate the equipment.