BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SENSIA DR

    MDR report key: 1013504 · Received March 10, 2008

    Report

    Report Number
    6000094-2008-00071
    Event Type
    Malfunction
    Date Received
    March 10, 2008
    Manufacturer
    MEDTRONIC S.A.
    Product Code
    NVZ
    Removal / Correction Number
    NI
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    INVALID DATA

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SENSIA DR IMPLANTABLE PULSE GENERATOR NVZ MEDTRONIC S.A. SEDR01 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other