BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    2921578-1997-00003

    MDR report key: 112609 · Received August 8, 1997

    Report

    Report Number
    2921578-1997-00003
    Event Type
    Malfunction
    Date Received
    August 8, 1997
    Date of Event
    April 1, 1997
    Product Code
    FQO
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1