BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1163224 · Received July 8, 2008

    Report

    Report Number
    8010042-2008-00093
    Event Type
    Malfunction
    Date Received
    July 8, 2008
    Manufacturer
    MAQUET CRITICAL CARE AB
    Product Code
    CBK
    PMA / PMN Number
    k970839
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * CBK MAQUET CRITICAL CARE AB * *

    Patients

    Seq Age Sex Outcome Treatment
    1