BEUDAMED
    108 results · 41ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    EPILIGHT

    FDA Adverse Event
    Injury ·LUMENIS, (ISRAEL)·Product code GEX·August 5, 2005

    SLIMLINE 550 FIBER

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·May 7, 2014

    LUMENIS ONE

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

    SLIM LINE SIS 365

    FDA Adverse Event
    Injury ·LUMENIS, LTD.·Product code GEX·August 28, 2013

    LUMENISONE

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

    LIGHTSHEER XC

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

    SPLENDOR X

    FDA Adverse Event
    Injury ·BIOS S.R.L·Product code GEX·June 13, 2025

    SLIMLINE 550

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

    QUANTUM

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·May 11, 2006

    TRILIFT

    FDA Adverse Event
    Injury ·POLLOGEN LTD·Product code NGX·September 23, 2023

    SLIMLINE FIBER

    FDA Adverse Event
    Injury ·LUMENIS LTD.·Product code GEX·December 4, 2017

    LIGHTSHEER DUET

    FDA Adverse Event
    Injury ·RH USA, INC.·Product code GEX·January 26, 2011

    SPLENDOR X

    FDA Adverse Event
    Injury ·BIOS SRL·Product code GEX·June 9, 2025

    SPLENDOR X

    FDA Adverse Event
    Injury ·BIOS SRL·Product code GEX·June 9, 2025

    LIGHTSHEER DUET

    FDA Adverse Event
    Injury ·LUMENIS INC.·Product code GEX·January 19, 2012

    LUMENIS ONE

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·November 30, 2011

    M22

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

    M22

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

    LIGHTSHEER

    FDA Adverse Event
    Injury ·LUMENIS LTD.·Product code GEX·January 27, 2019

    LIGHSHEER DUET

    FDA Adverse Event
    Injury ·LUMENIS BE LTD.·Product code GEX·December 14, 2022