BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GREENLIGHT ADDSTAT

    MDR report key: 1950417 · Received December 14, 2010

    Report

    Report Number
    2937094-2010-01283
    Event Type
    Malfunction
    Date Received
    December 14, 2010
    Date of Event
    June 17, 2009
    Report Date
    November 17, 2010
    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 THE CUSTOMER THAT ON (B)(6) 2009, THE FIBER WAS DAMAGED AT AN UNKNOWN AMOUNT OF JOULES. THE DEVICE WAS NOT RETURNED FOR EVALUATION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMS INNOVATION CENTER - SILICON VALLEY NA 930U

    Patients

    Seq Age Sex Outcome Treatment
    1 Other