BEUDAMED
    FDA Adverse Event Other Summary report: N

    1018233-2012-00371

    MDR report key: 6984774 · Received October 27, 2017

    Report

    Report Number
    1018233-2012-00371
    Event Type
    Other
    Date Received
    October 27, 2017
    Report Date
    October 27, 2017
    Manufacturer
    C.R. BARD, INC.
    PMA / PMN Number
    K082571
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    ATTORNEY
    Health Professional
    N

    Patients

    Seq Age Sex Outcome Treatment
    1 51 YR Female Required Intervention ALIGN URETHRAL SUPPORT SYSTEM