BEUDAMED
    FDA Adverse Event Summary report: N

    1810909-2000-00003

    MDR report key: 260611 · Received January 18, 2000

    Report

    Report Number
    1810909-2000-00003
    Date Received
    January 18, 2000
    Date of Event
    December 8, 1999
    Product Code
    FMK
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FMK

    Patients

    Seq Age Sex Outcome Treatment
    1