oticon TVA3, Инструкция по эксплуатации

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48 49 About Installation Handling Warnings More info
The manufacturer declares that this
TV adapter 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
from the manufacturer.
SBO Hearing A/S
Kongebakken 9
DK-2765 Smørum
Denmark
Waste from electronic
equipment must be
handled according to
local regulations.
Description of symbols and abbreviation used in this booklet
Warnings
Text marked with a warning symbol must be read before using the device.
Manufacturer
The device is produced by the manufacturer whose name and address are stated
next to the symbol. Indicates the medical device manufacturer, as defined in EU
Regulations 2017/745 and 2017/746.
CE mark
The device complies with all required EU regulations and directives.
Electronic waste (WEEE)
Recycle hearing aids, accessories or batteries according to local regulations.
Hearing aid users can also return electronic waste to their hearing care
professional for disposal. Electronic equipment covered by Directive 2012/19/EU
on waste and electrical equipment (WEEE).
Regulatory Compliance Mark (RCM)
The device complies with electrical safety, EMC and radio spectrum requirements
for devices supplied to the Australian or New Zealand market.
Double insulation
Indicates that product power supply is double insulated. This means a very low
risk of single fault failures i.e. single fault failures cannot occur.