BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2250051-2008-00077

    MDR report key: 1012546 · Received February 8, 2008

    Report

    Report Number
    2250051-2008-00077
    Event Type
    Malfunction
    Date Received
    February 8, 2008
    Product Code
    JTC
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 JTC

    Patients

    Seq Age Sex Outcome Treatment
    1