BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GREENLIGHT ADDSTAT

    MDR report key: 2092693 · Received May 2, 2011

    Report

    Report Number
    2937094-2011-00884
    Event Type
    Malfunction
    Date Received
    May 2, 2011
    Date of Event
    May 25, 2010
    Report Date
    April 12, 2011
    Manufacturer
    AMS, INNOVATION CENTER - SILICON VALLEY
    Product Code
    GEX
    PMA / PMN Number
    K062719
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY A CUSTOMER ON (B)(6) 2010 NO COAGULATION OCCURRED FROM THE FIBER AT 41,766 JOULES. ALSO, IT WAS REPORTED THAT NO ERROR MESSAGE OCCURRED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMS, INNOVATION CENTER - SILICON VALLEY NA 948N

    Patients

    Seq Age Sex Outcome Treatment
    1 Other