BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 1146028 · Received August 26, 2008

    Report

    Report Number
    8010652-2008-00006
    Event Type
    Other
    Date Received
    August 26, 2008
    Manufacturer
    MAQUET GMBH AND CO. KG
    Product Code
    FWZ
    PMA / PMN Number
    EXEMPT
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * FWZ MAQUET GMBH AND CO. KG * *

    Patients

    Seq Age Sex Outcome Treatment
    1