BEUDAMED
    FDA Adverse Event Other Summary report: N

    ESTEEM

    MDR report key: 3252597 · Received July 19, 2013

    Report

    Report Number
    3004007782-2013-00047
    Event Type
    Other
    Date Received
    July 19, 2013
    Date of Event
    January 10, 2013
    Report Date
    July 19, 2013
    Manufacturer
    ENVOY MEDICAL
    Product Code
    OAF
    PMA / PMN Number
    P090018
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THIS PT REPORTED SOME FORM OF TASTE DISTURBANCE THAT PERSISTED AFTER THE FIRST FITTING AFTER ACTIVATION. NO DEVICE WAS RETURNED FOR ANALYSIS. THE CHORDA TYMPANI IS USUALLY DIVIDED DURING THE IMPLANT PROCEDURE. THE PT IS SPECIFICALLY ADVISED OF THIS PRIOR TO THE PROCEDURE.

    Description of Event or Problem · 1

    THIS PT REPORTED SOME FORM OF TESTS DISTURBANCE DURING A FITTING APPOINTMENT WITH THEIR AUDIOLOGIST. NO OTHER DETAILS WERE PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    338111 ESTEEM OAF ENVOY MEDICAL 2001 EMC0004438

    Patients

    Seq Age Sex Outcome Treatment
    1 37 YR Other