BEUDAMED
    FDA Adverse Event Injury Summary report: N

    8022037-1998-90001

    MDR report key: 178578 · Received July 23, 1998

    Report

    Report Number
    8022037-1998-90001
    Event Type
    Injury
    Date Received
    July 23, 1998
    Date of Event
    January 28, 1998
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1