BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    7900

    MDR report key: 2081903 · Received April 5, 2011

    Report

    Report Number
    9680959-2011-00958
    Event Type
    Malfunction
    Date Received
    April 5, 2011
    Date of Event
    February 3, 2011
    Report Date
    April 5, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS GMBH
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE GE REPRESENTATIVE CONDUCTED AN ONSITE EVALUATION. THE UPGRADE KIT WAS INSTALLED. THE SYSTEM WAS TESTED AND OPERATES AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE 7900 SYSTEM NEEDS A TRSL MODULE INSTALLED. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 7900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS GMBH 7900

    Patients

    Seq Age Sex Outcome Treatment
    1