BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1030186-1998-00001

    MDR report key: 164748 · Received April 24, 1998

    Report

    Report Number
    1030186-1998-00001
    Event Type
    Injury
    Date Received
    April 24, 1998
    Date of Event
    March 24, 1998
    Product Code
    KGX
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KGX NOT PROVIDED

    Patients

    Seq Age Sex Outcome Treatment
    1