BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1933441-1999-00002

    MDR report key: 241708 · Received September 21, 1999

    Report

    Report Number
    1933441-1999-00002
    Event Type
    Injury
    Date Received
    September 21, 1999
    Date of Event
    July 2, 1999
    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