BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8010042-2008-00068

    MDR report key: 1103623 · Received May 30, 2008

    Report

    Report Number
    8010042-2008-00068
    Event Type
    Malfunction
    Date Received
    May 30, 2008
    Product Code
    MOD
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1