A methodical evaluation of new CE-labelled Phonak Hearing Systems is intended to be conducted on hard of participants with a hearing loss to grant quality control prior to product launch. The aim of the investigation series is to ensure usability, zero-defect overall performance of the new hearing systems as well as maximum benefit for the participant with the devices in comparison to previously outstanding Phonak Hearing Systems.
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Usability (phone calls)
Timeframe: One week