BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    9800

    MDR report key: 3911887 · Received May 13, 2014

    Report

    Report Number
    1720753-2014-04138
    Event Type
    Malfunction
    Date Received
    May 13, 2014
    Date of Event
    April 22, 2014
    Report Date
    May 13, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    BR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO CONCLUSION CAN BE DRAWN AS REPAIR INFO IS UNAVAILABLE.

    Description of Event or Problem · 1

    THE CUSTOMER DESCRIBED WHAT WAS LIKELY A SYSTEM LOCK UP SITUATION. THERE ARE NO REPORTS OF PT INJURY OR DEATH ASSOCIATED WITH THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    285317 9800 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) 9800

    Patients

    Seq Age Sex Outcome Treatment
    1