BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 1240487 · Received August 29, 2008

    Report

    Report Number
    3003135857-2008-00048
    Event Type
    Other
    Date Received
    August 29, 2008
    Manufacturer
    *
    Product Code
    CBK
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1