BEUDAMED
    2,083 results · 32ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    LUMENIS PULSE 120H

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

    VERSAPULSE POWERSUITE 100W

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

    SLIMLINE 550¿ FIBER

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

    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

    EPLIGHT

    FDA Adverse Event
    Injury ·LUMENIS·Product code GEX·October 13, 2006

    LUMENIS ONE

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·September 6, 2013

    VASCULIGHT SR

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·March 16, 2012

    ULTRAPULSE ENCORE

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·October 25, 2012

    ULTRAPULSE ENCORE AESTHETIC PACKAGE

    FDA Adverse Event
    Injury ·LUMENIS LTD. YOKNEAM·Product code GEX·October 27, 2010

    LIGHTSHEER DESIRE

    FDA Adverse Event
    Injury ·LUMENIS BE LTD·Product code GEX·October 19, 2025

    SPLENDOR X

    FDA Adverse Event
    Injury ·BIOS SRL·Product code GEX·January 8, 2026

    VASCULIGHT HR

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·January 18, 2012

    LIGHTSHEER

    FDA Adverse Event
    Injury ·RH USA, INC.·Product code GEX·June 2, 2009

    SLIMLINE 550

    FDA Adverse Event
    Injury ·LUMENIS LTD.·Product code GEX·March 12, 2007

    LIGHTSHEER XC

    FDA Adverse Event
    Injury ·RH USA, INC.·Product code GEX·October 31, 2012