BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ZIMMER AIR DERMATOME

    MDR report key: 1040992 · Received April 7, 2008

    Report

    Report Number
    1526350-2008-00024
    Event Type
    Malfunction
    Date Received
    April 7, 2008
    Product Code
    GFD
    Adverse Event
    Yes
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ZIMMER AIR DERMATOME AIR DERMATOME GFD

    Patients

    Seq Age Sex Outcome Treatment
    1