BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2250051-2006-00140

    MDR report key: 695792 · Received April 3, 2006

    Report

    Report Number
    2250051-2006-00140
    Event Type
    Malfunction
    Date Received
    April 3, 2006
    Product Code
    GHM
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1