BEUDAMED
    FDA Adverse Event Other Summary report: N

    1933078-1998-00001

    MDR report key: 173058 · Received June 19, 1998

    Report

    Report Number
    1933078-1998-00001
    Event Type
    Other
    Date Received
    June 19, 1998
    Product Code
    DJZ
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1