BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9900

    MDR report key: 3882783 · Received April 10, 2014

    Report

    Report Number
    1720753-2014-03115
    Event Type
    Malfunction
    Date Received
    April 10, 2014
    Date of Event
    March 23, 2014
    Report Date
    April 10, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IS
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE REPRESENTATIVE EVALUATED THE SYSTEM BUT NO CONCLUSION CAN BE DRAWN AS FURTHER REPAIR INFORMATION IS NOT AVAILABLE.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED LOSING THE FIRST THREE SECONDS OF THE CINE RUN. (DATA LOSS). THERE IS NO REPORT OF INJURY OR DEATH.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    216284 9900 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9900

    Patients

    Seq Age Sex Outcome Treatment
    1