BEUDAMED
    FDA Adverse Event Injury Summary report: N

    2132280-2002-00001

    MDR report key: 401917 · Received June 19, 2002

    Report

    Report Number
    2132280-2002-00001
    Event Type
    Injury
    Date Received
    June 19, 2002
    Date of Event
    May 24, 2002
    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