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About Start-up Handling Warnings More info
Waste from electronic
equipment must be
handled according to
local regulations.
The manufacturer declares that this
charger C-1A | C-1A2 is in compliance
with the essential requirements and
other relevant provisions of Directive
EMC (2014/30/EU) and LVD (2014/35/
EU).
This medical device complies with
the Medical Device Regulation (EU)
2017/745.
Declaration of Conformity is available
from the headquarters:
Oticon A/S
Kongebakken 9
DK-2765 Smørum
Denmark
www.oticon.global/doc
SBO Hearing A/S
Denmark
However, there is no guarantee that
interference will not occur in a particular
installation. If this equipment does
cause harmful interference to other
electronic equipment, which can be
determined by turning the equipment
OFF and ON, the user is encouraged to
try to correct the interference by one or
more of the following measures:
• Reorient or relocate the equipment
• Increase the separation between the
equipment
Changes or modifications not expressly
approved by the party responsible
for compliance could void the user’s
authority to operate the equipment.
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