BEUDAMED
    FDA Adverse Event Summary report: N

    2132280-2001-00002

    MDR report key: 315886 · Received January 31, 2001

    Report

    Report Number
    2132280-2001-00002
    Date Received
    January 31, 2001
    Date of Event
    January 22, 2001
    Product Code
    FSA
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3827 FSA

    Patients

    Seq Age Sex Outcome Treatment
    1