BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8010042-2008-00136

    MDR report key: 1240563 · Received August 26, 2008

    Report

    Report Number
    8010042-2008-00136
    Event Type
    Malfunction
    Date Received
    August 26, 2008
    Product Code
    CBK
    PMA / PMN Number
    K041223
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1