BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GREENLIGHT ADDSTAT

    MDR report key: 1844061 · Received September 13, 2010

    Report

    Report Number
    2937094-2010-00111
    Event Type
    Malfunction
    Date Received
    September 13, 2010
    Date of Event
    February 25, 2010
    Report Date
    April 29, 2010
    Manufacturer
    AMS INNOVATION CENTER-SILICON VALLEY
    Product Code
    GEX
    PMA / PMN Number
    K062719
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE CUSTOMER THAT ON (B)(6) 2010, THE FIBER TIP DETACHED INSIDE THE PT AT 86,882 JOULES AND THAT THE FIBER TIP WAS TOO SMALL TO RETRIEVE. THE CUSTOMER REPORTED THAT NO PT INJURY OCCURRED. THE DEVICE WAS NOT RETURNED FOR EVAL.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 Other