BEUDAMED
    FDA Adverse Event Other Summary report: N

    VERSAPULSE AESTHETIC C

    MDR report key: 226427 · Received June 3, 1999

    Report

    Report Number
    2914019-1999-00002
    Event Type
    Other
    Date Received
    June 3, 1999
    Date of Event
    May 4, 1999
    Report Date
    May 6, 1999
    Manufacturer
    COHERENT MEDICAL GROUP
    Product Code
    GEX
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    A FIELD SERVICE ENGINEER WAS SERVICING A VERSAPULSE LASER WHEN A REFLECTED BEAM HIT HIS EYE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VERSAPULSE AESTHETIC C LASER GEX COHERENT MEDICAL GROUP NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 31 YR Required Intervention