BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    7700

    MDR report key: 2023518 · Received March 1, 2011

    Report

    Report Number
    9680959-2011-00609
    Event Type
    Malfunction
    Date Received
    March 1, 2011
    Date of Event
    June 18, 2010
    Report Date
    March 1, 2011
    Manufacturer
    GE OEC MEDICAL SYSTEMS GMBH
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FR
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 1

    THE MANUFACTURER'S SERVICE REPRESENTATIVE PERFORMED AN ON SITE INVESTIGATION. THE SERVICE REPRESENTATIVE REPLACED THE CONNECTOR PINS. THE SYSTEM IS OPERATING AS INTENDED.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED THAT THE 7700 SYSTEM WAS HAVING PROBLEMS WITH MECHANICAL MOVEMENTS. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 7700 FLUOROSCOPIC X-RAY JAA GE OEC MEDICAL SYSTEMS GMBH 7700

    Patients

    Seq Age Sex Outcome Treatment
    1