BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8010047-1997-00004

    MDR report key: 64436 · Received January 20, 1997

    Report

    Report Number
    8010047-1997-00004
    Event Type
    Malfunction
    Date Received
    January 20, 1997
    Date of Event
    November 12, 1996
    Product Code
    KOG
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1