BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GYNEMESH POLYPROPYLENE MESH

    MDR report key: 2050318 · Received April 6, 2011

    Report

    Report Number
    MW5020208
    Event Type
    Injury
    Date Received
    April 6, 2011
    Date of Event
    May 19, 2006
    Report Date
    April 6, 2011
    Manufacturer
    UNK
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    GYNEMESH POLYPROPYLENE GRAFT INSERTED. SINCE THAT TIME, MARITAL RELATIONS ARE IMPOSSIBLE, PAIN AND FREQUENT UTIS HAVE OCCURRED REGULARLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GYNEMESH POLYPROPYLENE MESH MESH FTL UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Required Intervention