BEUDAMED
    FDA Adverse Event Injury Summary report: N

    1831750-1998-00014

    MDR report key: 188176 · Received September 18, 1998

    Report

    Report Number
    1831750-1998-00014
    Event Type
    Injury
    Date Received
    September 18, 1998
    Date of Event
    July 29, 1998
    Product Code
    KNC
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1