BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    KODAK M6AW

    MDR report key: 35485 · Received July 13, 1996

    Report

    Report Number
    35485
    Event Type
    Malfunction
    Date Received
    July 13, 1996
    Report Date
    July 12, 1996
    Manufacturer
    EASTMAN KODAK CO.
    Product Code
    IXW
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    NC, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    SCRATCHES ON X-RAY FILM. SERVICEMAN REPLACED "G" ROLLERS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 KODAK M6AW X-RAY PROCESSOR IXW EASTMAN KODAK CO. * *

    Patients

    Seq Age Sex Outcome Treatment
    1 NA
    2