BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2110898-1996-00005

    MDR report key: 45049 · Received October 25, 1996

    Report

    Report Number
    2110898-1996-00005
    Event Type
    Injury
    Date Received
    October 25, 1996
    Date of Event
    September 5, 1996
    Product Code
    DRX
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 *