BEUDAMED
    FDA Adverse Event Injury Summary report: N

    OBTAPE TRANSOBTURATOR SLING

    MDR report key: 5883821 · Received August 17, 2016

    Report

    Report Number
    1645337-2016-00123
    Event Type
    Injury
    Date Received
    August 17, 2016
    Report Date
    August 15, 2016
    Manufacturer
    MENTOR WW LLC
    Product Code
    PAH
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    ATTORNEY

    Narratives

    Additional Manufacturer Narrative · 1

    DEVICE NOT RETURNED.

    Description of Event or Problem · 1

    INJURIES. (LITIGATION CASE).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    535461 OBTAPE TRANSOBTURATOR SLING TRANSOBTURATOR PAH MENTOR WW LLC

    Patients

    Seq Age Sex Outcome Treatment
    1 Other