BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UROVIEW

    MDR report key: 1854064 · Received September 2, 2010

    Report

    Report Number
    1720753-2010-02906
    Event Type
    Malfunction
    Date Received
    September 2, 2010
    Date of Event
    August 23, 2010
    Report Date
    September 2, 2010
    Manufacturer
    GE OEC MEDICAL SYSTEMS (SLC)
    Product Code
    JAA
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE CUSTOMER CANCELLED THE SERVICE CALL. THEREFORE, NO CONCLUSION CAN BE DRAWN. HOWEVER, NO REPORTS OF PATIENT OR STAFF INJURIES.

    Description of Event or Problem · 1

    THE CUSTOMER REPORTED, THE TABLE FAILED TO MOVE LONGITUDINALLY. NO REPORTS OF PATIENT AND OR STAFF INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 UROVIEW FLUOROSCOPY XRAY JAA GE OEC MEDICAL SYSTEMS (SLC) 2800

    Patients

    Seq Age Sex Outcome Treatment
    1