BEUDAMED
    FDA Adverse Event Other Summary report: N

    1415191-2001-00002

    MDR report key: 334844 · Received May 23, 2001

    Report

    Report Number
    1415191-2001-00002
    Event Type
    Other
    Date Received
    May 23, 2001
    Date of Event
    January 14, 2000
    Product Code
    KNF
    Report Source
    Manufacturer report

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    24081 KNF

    Patients

    Seq Age Sex Outcome Treatment
    1