BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    1831750-1999-00004

    MDR report key: 222735 · Received May 5, 1999

    Report

    Report Number
    1831750-1999-00004
    Event Type
    Malfunction
    Date Received
    May 5, 1999
    Date of Event
    March 2, 1999
    Product Code
    FPO
    Report Source
    Manufacturer report

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1