BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 3791924 · Received January 3, 2014

    Report

    Report Number
    1720753-2014-00084
    Event Type
    Malfunction
    Date Received
    January 3, 2014
    Date of Event
    December 17, 2013
    Report Date
    January 3, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MI, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    A GE SERVICE REP PERFORMED AN ONSITE INVESTIGATION. IT WAS DETERMINED THAT THE SYSTEM NEEDS A NEW POWER SWITCH; THE PART WAS ORDERED. NO FURTHER REPAIR INFO IS AVAILABLE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE WORKSTATION WOULD NOT BOOT UP. THERE IS NO REPORT OF INJURY OR DEATH ASSOCIATED WITH THE EVENT DESCRIBED IN THIS COMPLAINT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    3893 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1