BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    STENOSCOP

    MDR report key: 3791850 · Received January 6, 2014

    Report

    Report Number
    1720753-2014-00105
    Event Type
    Malfunction
    Date Received
    January 6, 2014
    Date of Event
    December 18, 2013
    Report Date
    January 6, 2014
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    NO CONCLUSION CAN BE DRAWN AAS REPAIR INFO IS UNAVAILABLE.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE SYS COULD NOT FLUORO. IT WAS ALSO STATED THAT THE FAULT WAS CLEARED BY THE CUSTOMER. THIS CAUSED AN INTERMITTENT LOSS OF IMAGING FUNCTIONALITY. 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
    8592 STENOSCOP FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS (SLC) STENOSCOP

    Patients

    Seq Age Sex Outcome Treatment
    1