BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221826-2006-00062

    MDR report key: 796996 · Received October 17, 2006

    Report

    Report Number
    1221826-2006-00062
    Event Type
    Other
    Date Received
    October 17, 2006
    Product Code
    FGB
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1