BEUDAMED
    FDA Adverse Event Injury Summary report: N

    PROPLAST TEFLON IMPLANT

    MDR report key: 2820759 · Received October 29, 2012

    Report

    Report Number
    MW5027418
    Event Type
    Injury
    Date Received
    October 29, 2012
    Report Date
    October 29, 2012
    Product Code
    FWM
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OR, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I RECEIVED A PROPLAST TEFLON TMJ IMPLANT WHEN I WAS A YOUNG GIRL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 PROPLAST TEFLON IMPLANT TMJ IMPLANT FWM

    Patients

    Seq Age Sex Outcome Treatment
    1 Hospitalization| S