BEUDAMED
    FDA Adverse Event Other Summary report: N

    1831750-2003-00009

    MDR report key: 452930 · Received April 9, 2003

    Report

    Report Number
    1831750-2003-00009
    Event Type
    Other
    Date Received
    April 9, 2003
    Date of Event
    February 3, 2003
    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