BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1933441-1997-00005

    MDR report key: 135810 · Received December 2, 1997

    Report

    Report Number
    1933441-1997-00005
    Event Type
    Injury
    Date Received
    December 2, 1997
    Date of Event
    September 24, 1997
    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