BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2023337-1998-00001

    MDR report key: 204224 · Received December 22, 1998

    Report

    Report Number
    2023337-1998-00001
    Event Type
    Injury
    Date Received
    December 22, 1998
    Date of Event
    October 9, 1998
    Product Code
    FOA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1