BEUDAMED
    FDA Adverse Event Injury Summary report: N

    URETEX TO3 URETHRAL SUPPORT SYSTEM

    MDR report key: 3172282 · Received April 26, 2013

    Report

    Report Number
    1018233-2013-01583
    Event Type
    Injury
    Date Received
    April 26, 2013
    Report Date
    March 27, 2013
    Manufacturer
    SOFRADIM PRODUCTION
    Product Code
    FTL
    Adverse Event
    Yes
    Report Source
    Distributor report
    Reporter Location
    MO, US
    Reporter Occupation
    ATTORNEY

    Narratives

    Description of Event or Problem · 1

    THE PATIENT'S ATTORNEY ALLEGED A DEFICIENCY AGAINST THE DEVICE. ADDITIONAL INFORMATION HAS BEEN REQUESTED, BUT NOT YET RECEIVED. ASSOCIATED MDR # 1018233-2013-01584.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    183252 URETEX TO3 URETHRAL SUPPORT SYSTEM FTL SOFRADIM PRODUCTION NA SFK00118

    Patients

    Seq Age Sex Outcome Treatment
    1 75 YR Required Intervention AVAULTA ANTERIOR BIOSYNTHETIC SUPPORT SYSTEM