BEUDAMED
    FDA Adverse Event Other Summary report: N

    9610617-2000-00026

    MDR report key: 302640 · Received October 27, 2000

    Report

    Report Number
    9610617-2000-00026
    Event Type
    Other
    Date Received
    October 27, 2000
    Date of Event
    September 12, 2000
    Product Code
    FFL
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1