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Unitron DX Insera 3 W 312 Dir Guide D'utilisation page 33

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Date of manufacture
Serial number
Transportation and storage temperature limitation
Transportation and storage humidity limitation
Transportation and storage atmospheric pressure
limitation
Keep dry
54
Compliance information
Declaration of conformity
Hereby, Sonova AG declares that this product meets the
requirements of the Medical Device Directive 93/42/EEC and
complies with Radio Equipment Directive 2014/53/EU. The full
text of the Declarations of Conformity can be obtained from the
manufacturer via the following web address:
https://unitron.com/content/certificates
Australia/New Zealand:
Indicates a device's compliance with applicable
Radio Spectrum Management's (RSM) and Australian
Communications and Media Authority (ACMA) regulatory
arrangements for the legal sale in New Zealand and
Australia. The compliance label R-NZ is for radio
products supplied in the New Zealand market under
conformity level A1.
The hearing aid described in this user guide is certified under:
Standard hearing system
USA - FCC ID:
DX Insera ITE 312 (Right)
KWC-IND
DX Insera ITE 312 (Left)
KWC-IND
Notice 1
This device complies with Part 15 of the FCC Rules and with RSS-
210 of Industry Canada. Operation is subject to the following two
conditions:
Canada - IC:
2262A-INR
2262A-IND
55

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