BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SENSIA SR

    MDR report key: 1072953 · Received July 10, 2008

    Report

    Report Number
    6000094-2008-00285
    Event Type
    Injury
    Date Received
    July 10, 2008
    Date of Event
    April 1, 2008
    Manufacturer
    MEDTRONIC S.A.
    Product Code
    NVZ
    Removal / Correction Number
    NI
    Report Source
    Manufacturer report
    Reporter Location
    JA
    Reporter Occupation
    PHYSICIAN

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SENSIA SR IMPLANTABLE PULSE GENERATOR NVZ MEDTRONIC S.A. SESR01 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 80 YR Other