BEUDAMED
    FDA Adverse Event Injury Summary report: N

    GEM III DR

    MDR report key: 1072978 · Received July 10, 2008

    Report

    Report Number
    6000094-2008-00329
    Event Type
    Injury
    Date Received
    July 10, 2008
    Date of Event
    March 13, 2008
    Manufacturer
    MEDTRONIC S.A.
    Product Code
    LWS
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GEM III DR IMPLANTABLE PACEMAKER/CARDIO/DEFIB LWS MEDTRONIC S.A. 7275 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Required Intervention