BEUDAMED
    FDA Adverse Event Injury Summary report: N

    8010042-2008-00049

    MDR report key: 1100743 · Received April 16, 2008

    Report

    Report Number
    8010042-2008-00049
    Event Type
    Injury
    Date Received
    April 16, 2008
    Product Code
    CAH
    PMA / PMN Number
    K030071
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1