BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1423537-1997-00104

    MDR report key: 103067 · Received July 2, 1997

    Report

    Report Number
    1423537-1997-00104
    Event Type
    Malfunction
    Date Received
    July 2, 1997
    Date of Event
    May 5, 1997
    Product Code
    KBE
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1