BEUDAMED
    FDA Adverse Event Other Summary report: N

    SURGICAL LIGHTS

    MDR report key: 466859 · Received June 16, 2003

    Report

    Report Number
    1043572-2003-00005
    Event Type
    Other
    Date Received
    June 16, 2003
    Date of Event
    March 18, 2003
    Report Date
    June 13, 2003
    Manufacturer
    STERIS CORPORATION - MONTGOMERY
    Product Code
    FQP
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SURGICAL LIGHTS * FQP STERIS CORPORATION - MONTGOMERY 2075420 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Other