BEUDAMED
    52 results · 32ms · Sources: EU EUDAMED, US FDA

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    VERSAPULSE SELECT

    FDA Adverse Event
    Other ·COHERENT MEDICAL GROUP·Product code GEX·June 28, 2005

    LIGHTSHEER SYSTEM

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 11, 2002

    LIGHTSHEER

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·September 2, 2003

    LUMENIS

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·August 21, 2003

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·May 9, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·April 3, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·April 3, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·April 3, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·May 8, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·April 4, 2007

    COR18001652-000

    FDA Adverse Event
    Other ·Lumenis, Inc.·Product code GEX·October 18, 2018

    ULTRAPULSE XL 3000/5000

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·March 30, 2007

    LIGHTSHEER ET

    FDA Adverse Event
    Other ·LUMENIS INC.·Product code GEX·March 13, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 19, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 5, 2007

    LIGHTSHEER ET

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 3, 2007

    LIGHTSHEER

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 3, 2007

    QUANTUM

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·February 12, 2007

    LIGHTSHEER ET

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 3, 2007

    VERSAPULSE VPW-110V

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·March 6, 2007