BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SUREFLEX LASER FIBER

    MDR report key: 1970956 · Received January 6, 2011

    Report

    Report Number
    2937094-2010-01529
    Event Type
    Malfunction
    Date Received
    January 6, 2011
    Date of Event
    December 16, 2010
    Report Date
    December 16, 2010
    Manufacturer
    AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY
    Product Code
    GEX
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY THE CUSTOMER THAT ON (B)(6) 2010, THE FIBER BROKE AT THE DISTAL END DURING THE PROCEDURE. NO PT INJURY WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SUREFLEX LASER FIBER SUREFLEX FIBER GEX AMERICAN MEDICAL SYSTEMS, INNOVATION CENTER - SILICON VALLEY NA TRF3629B

    Patients

    Seq Age Sex Outcome Treatment
    1 Other