BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3113083 · Received May 9, 2013

    Report

    Report Number
    1720753-2013-05854
    Event Type
    Malfunction
    Date Received
    May 9, 2013
    Date of Event
    May 2, 2013
    Report Date
    May 9, 2013
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. NO FURTHER REPAIR INFO IS AVAILABLE AT THIS TIME.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE SYSTEM MASKING FUNCTION WAS NOT WORKING AND THEY COULDN'T SEE HALF OF THE AREA OF INTEREST IN THE DISPLAYED IMAGE. THIS ISSUE CREATED AN UNUSABLE IMAGE. THERE IS NO REPORT OF PT INJURY ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    202707 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1