BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 252030 · Received November 26, 1999

    Report

    Report Number
    9614969-1999-00002
    Event Type
    Other
    Date Received
    November 26, 1999
    Date of Event
    October 15, 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