Phonak Roger NeckLoop 02 User Manual page 18

Any serious incident that has occurred in relation to the
device should be reported to the manufacturer
representative and the competent authority of the state
of residence. The serious incident is described as any
incident that directly or indirectly led, might have led or
might lead to any of the following:
the death of a patient, user or other person, the
temporary or permanent serious deterioration of a
patient's, user's or other person's state of health, a serious
public health threat.
To report an unexpected operation or event, please
contact the manufacturer or a representative.
Diligent and routine care of your device contributes to
outstanding performance and a long service life. To
ensure a long service life, Sonova AG provides a minimum
of a five year service period after phase out of the
respective product.
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For more information regarding features, benefits, setup,
use and maintenance or repairs of your accessories –
contact your hearing care professional or manufacturer
representative. Additional information can be found in the
Data Sheet of your product.
For any information regarding the repair service of the
hearing aid accessories please contact the hearing care
professional.
Intended use:
Neck loop receivers are intended to provide access to an
external sound source.
Indication: Neck loop receivers do not provide a
therapeutic or diagnostic function. The therapeutic
function is solely provided by the parent medical device
(e.g. hearing aid or cochlea implant), which receives and
further processes the inductive signal provided by the
neck loop. Therefore, the neck loop itself has no own
clinical indication.
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