BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1933441-1999-00003

    MDR report key: 269503 · Received March 13, 2000

    Report

    Report Number
    1933441-1999-00003
    Event Type
    Injury
    Date Received
    March 13, 2000
    Date of Event
    October 23, 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