BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 1210996 · Received July 23, 2008

    Report

    Report Number
    3003135857-2008-00046
    Event Type
    Malfunction
    Date Received
    July 23, 2008
    Manufacturer
    FLIGHT MEDICAL LTD.
    Product Code
    CBK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * * CBK FLIGHT MEDICAL LTD. * *

    Patients

    Seq Age Sex Outcome Treatment
    1