BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MINIARC SLING

    MDR report key: 3131153 · Received May 22, 2013

    Report

    Report Number
    MW5030276
    Event Type
    Injury
    Date Received
    May 22, 2013
    Date of Event
    April 18, 2013
    Report Date
    May 22, 2013
    Manufacturer
    UNK
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MI, US
    Reporter Occupation
    PHYSICIAN ASSISTANT

    Narratives

    Description of Event or Problem · 1

    PRIOR MINIARC SLING PT EXPERIENCED PAIN, DYSPAREUNIA, AND DESIRED REMOVAL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    226825 MINIARC SLING SLING FTL UNK UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 62 YR