BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GREENLIGHT ADDSTAT

    MDR report key: 2022096 · Received February 28, 2011

    Report

    Report Number
    2937094-2011-00229
    Event Type
    Malfunction
    Date Received
    February 28, 2011
    Date of Event
    January 28, 2011
    Report Date
    February 1, 2011
    Manufacturer
    AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY
    Product Code
    GEX
    PMA / PMN Number
    K100746
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY A CUSTOMER ON (B)(6) 2011, WHEN THE FIBER WAS UNPACKAGED, THE FIBER WAS DAMAGED AT THE TIP; THERE WAS A FRAYED OUTER PLASTIC LAYER AT THE TIP OF THE FIBER AT 0 JOULES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GREENLIGHT ADDSTAT SURGICAL FIBER GEX AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY NA 052A

    Patients

    Seq Age Sex Outcome Treatment
    1 Other