BEUDAMED
    8,425 results · 44ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    VERSAPULSE POWERSUITE 20W

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

    LUMENIS PULSE 120H

    FDA Adverse Event
    Injury ·LUMENIS, LTD·Product code GEX·February 22, 2017

    LUMENIS 1

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

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·February 20, 2007

    FRAXEL

    FDA Adverse Event
    SOLTA MEDICAL, INC.·Product code GEX·May 20, 2011

    EPILIGHT

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

    LUMENIS PULSE 30H

    FDA Adverse Event
    Malfunction ·LUMENIS LTD.·Product code GEX·November 29, 2020

    FORTEC SMARTSCOPE 200U BARE HOLMIUM FIBER

    FDA Adverse Event
    Malfunction ·FORTEC MEDICAL.·Product code GEX·April 25, 2016

    VERSAPULSE POWERSUITE 100W

    FDA Adverse Event
    Injury ·LUMENIS LTD.·Product code GEX·September 27, 2017

    INFRATOME 30 DEGREE

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·September 11, 2006

    LUMENIS ONE

    FDA Adverse Event
    Malfunction ·LUMENIS, LTD.·Product code GEX·January 11, 2013

    SLIMLINE 550¿ FIBER

    FDA Adverse Event
    Injury ·LUMENIS LTD.·Product code GEX·December 26, 2017

    LUMENIS PULSE 120H

    FDA Adverse Event
    Malfunction ·LUMENIS LTD.·Product code GEX·September 11, 2017

    LIGHTSHEER ET

    FDA Adverse Event
    Injury ·RH USA, INC.·Product code GEX·December 14, 2012

    LIGHTSHEER

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·August 15, 2013

    LUMENIS ONE

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

    M22

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·September 25, 2014

    LUMENISONE

    FDA Adverse Event
    Injury ·LUMENIS LTD.·Product code GEX·March 13, 2007

    LUMENIS ONE

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·August 30, 2017

    SPLENDOR X

    FDA Adverse Event
    Injury ·BIOS SRL·Product code GEX·December 17, 2023