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CR310 REMOTE CONTROL USER GUIDE FOR KANSO® 2
Certification and applied standards
The CR310 Remote Control fulfils the essential requirements
listed in Annex 1 of the EC directive 90/385/EEC on Active
Implantable Medical Devices as per the conformity
assessment procedure in Annex 2.
The year in which authorisation to affix the CE mark was
granted was 2017.
The CR310 Remote Control also fulfils the essential
requirements listed in the EC directive 2014/53/EU on Radio
Equipment as per the conformity assessment procedure in
Annex III. The declaration of conformity may be consulted at
www.cochlear.com/wps/wcm/connect/intl/about/company-
information/declaration-of-conformity
FCC (Federal Communications Commission)
and Canadian ISED compliance
This device complies with part 15 of the FCC Rules and with
RSS-210 of Innovation, Science and Economic Development
Canada. Operation is subject to the following two conditions:
• This device may not cause harmful interference.
• This device must accept any interference received,
including interference that may cause undesired operation.
Changes or modifications made to this equipment not
expressly approved by Cochlear Limited may void the FCC
authorisation to operate this equipment.