BEUDAMED
    80 results · 35ms · Sources: EU EUDAMED, US FDA

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    COR21000303-000

    FDA Adverse Event
    Other ·Lumenis Ltd.·Product code GEX·October 7, 2021

    DUO TORNE SIDELITE 550

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

    LUMENIS 1

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

    ULTRAPULSE XL 3000/5000

    FDA Adverse Event
    Other ·LUMENIS LTD.·Product code GEX·April 2, 2007

    VASCULIGHT HR

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

    SURGICAL FIBER

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·May 7, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·April 25, 2007

    VASCULIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·April 30, 2007

    COR21000123-000

    FDA Adverse Event
    Other ·Lumenis Ltd.·Product code GEX·April 25, 2021

    COR21000292-000

    FDA Adverse Event
    Other ·Lumenis Ltd.·Product code GEX·September 29, 2021

    COR20000272-000

    FDA Adverse Event
    Other ·Lumenis Ltd.·Product code GEX·November 1, 2020

    COR22000092-000

    FDA Adverse Event
    Other ·Lumenis Ltd.·Product code GEX·May 25, 2022

    COR18001629-000

    FDA Adverse Event
    Other ·Lumenis Ltd.·Product code EWG·October 10, 2018

    QUANTUM

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·October 30, 2008

    IPL QUANTUM

    FDA Adverse Event
    Other ·LUMENIS, LTD·Product code GEX·October 2, 2008

    LUMENIS ONE

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·October 9, 2008

    VASCULIGHT ELITE

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·March 16, 2007

    SLIMLINE 365

    FDA Adverse Event
    Other ·LUMENIS LTD.·Product code GEX·March 15, 2007

    EPILIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·January 8, 2007

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·February 21, 2007