BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GE OEC 2600

    MDR report key: 1201744 · Received October 21, 2008

    Report

    Report Number
    1720753-2008-25468
    Event Type
    Malfunction
    Date Received
    October 21, 2008
    Date of Event
    August 13, 2008
    Report Date
    September 4, 2008
    Manufacturer
    GE OEC MEDICAL SYSTEMS INC.
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REP EVALUATED THE SYSTEM AND REPLACED THE IMAGE INTENSIFIER POWER SUPPLY. SYSTEM OPERATES AS INTENDED.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THE SYSTEM IS NOT PRODUCING AN IMAGE. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GE OEC 2600 NONE JAA GE OEC MEDICAL SYSTEMS INC. 2600 NA

    Patients

    Seq Age Sex Outcome Treatment
    1