BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8010047-1997-00003

    MDR report key: 64414 · Received January 20, 1997

    Report

    Report Number
    8010047-1997-00003
    Event Type
    Malfunction
    Date Received
    January 20, 1997
    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