BEUDAMED
    FDA Adverse Event Other Summary report: N

    9614969-1999-00003

    MDR report key: 265100 · Received February 16, 2000

    Report

    Report Number
    9614969-1999-00003
    Event Type
    Other
    Date Received
    February 16, 2000
    Date of Event
    December 9, 1999
    Product Code
    KNF
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1