BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    8010047-1996-00007

    MDR report key: 53979 · Received November 27, 1996

    Report

    Report Number
    8010047-1996-00007
    Event Type
    Malfunction
    Date Received
    November 27, 1996
    Date of Event
    October 9, 1996
    Product Code
    FDT
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1