BEUDAMED
    FDA Adverse Event Other Summary report: N

    *

    MDR report key: 582029 · Received February 28, 2005

    Report

    Report Number
    1043572-2005-00001
    Event Type
    Other
    Date Received
    February 28, 2005
    Date of Event
    November 15, 2004
    Report Date
    January 10, 2005
    Manufacturer
    STERIS CORP - MONTGOMERY
    Product Code
    FYD
    Report Source
    Manufacturer report
    Reporter Location
    WA, US

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * SURGICAL EXHAUST APPARATUS FYD STERIS CORP - MONTGOMERY 4654344 44-000468

    Patients

    Seq Age Sex Outcome Treatment
    1 UNKNOWN