BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2250051-2003-00340

    MDR report key: 474556 · Received July 24, 2003

    Report

    Report Number
    2250051-2003-00340
    Event Type
    Malfunction
    Date Received
    July 24, 2003
    Date of Event
    July 16, 2003
    Product Code
    GKH
    Removal / Correction Number
    NA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1