BEUDAMED
    FDA Adverse Event Other Summary report: N

    OHMEDA PHOTOTHERAPY LIGHT

    MDR report key: 504583 · Received December 17, 2003

    Report

    Report Number
    2018492-2003-00022
    Event Type
    Other
    Date Received
    December 17, 2003
    Date of Event
    September 1, 2003
    Report Date
    December 8, 2003
    Manufacturer
    BURTON MEDICAL PRODUCTS
    Product Code
    FSY
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OHMEDA PHOTOTHERAPY LIGHT PHOTOTHERAPY LIGHT FSY BURTON MEDICAL PRODUCTS 6600-0287-901 10/02 BURT

    Patients

    Seq Age Sex Outcome Treatment
    1 2 DAY Other