UNITRON STRIDE PRO HEARING AID

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-17 for UNITRON STRIDE PRO HEARING AID manufactured by Unitron.

MAUDE Entry Details

Report NumberMW5088220
MDR Report Key8803249
Date Received2019-07-17
Date of Event2017-01-02
Date Added to Maude2019-07-18
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationATTORNEY
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameUNITRON STRIDE PRO HEARING AID
Generic NameHEARING AID, AIR CONDUCTION WITH WIRELESS TECHNOLOGY
Product CodeOSM
Date Received2019-07-17
Model NumberSTRIDE PRO
Device Availability*
Device Eval'ed by MfgrI
Device Sequence No1
Device Event Key0
ManufacturerUNITRON


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-17

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