BEUDAMED
    FDA Adverse Event Injury Summary report: N

    6000043-1998-00096

    MDR report key: 193088 · Received October 21, 1998

    Report

    Report Number
    6000043-1998-00096
    Event Type
    Injury
    Date Received
    October 21, 1998
    Date of Event
    August 24, 1998
    Product Code
    FFL
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1