BEUDAMED
    170 results · 42ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    LUMENIS, INC

    FDA Adverse Event
    Injury ·LUMENIS, MFG·Product code GEX·December 31, 2008

    LUMENIS, INC.

    FDA Adverse Event
    Injury ·LUMENIS. LTD.·Product code GEX·November 20, 2008

    LUMENIS, INC

    FDA Adverse Event
    Injury ·LUMENIS, LTD·Product code GEX·January 22, 2009

    LUMENIS, INC.

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·August 25, 2008

    LUMENIS, INC.

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·August 25, 2008

    LUMENIS PULSE 120H

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 3, 2022

    LIGHTSHEER DUET HS/ET

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·April 28, 2022

    VERSAPULSE POWERSUITE 60W

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 3, 2022

    MOSES 200¿ D/F/L DISPOSABLE FIBER

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·May 3, 2022

    LIGHTSHEER XC

    FDA Adverse Event
    Injury ·LUMENIS LTD·Product code GEX·April 28, 2022

    LIGHTSHEER DUET

    FDA Adverse Event
    Injury ·LUMENIS INC.·Product code GEX·February 28, 2012

    LIGHTSHEER DUET

    FDA Adverse Event
    Injury ·LUMENIS INC.·Product code GEX·January 5, 2012

    LIGHTSHEER ET

    FDA Adverse Event
    Injury ·LUMENIS INC.·Product code GEX·February 22, 2012

    LIGHTSHEER DUET

    FDA Adverse Event
    Injury ·LUMENIS INC.·Product code GEX·January 3, 2012

    SELECTA II 110V

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·April 10, 2014

    SELECTA II

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code HQF·January 11, 2010

    SELECTA II 110V

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·April 10, 2014

    SELECTA DUET (ELLEX)

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·April 11, 2014

    SELECTA DUET

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·June 30, 2010

    VERSACUT TISSUE MORCELLATOR

    FDA Adverse Event
    Injury ·LUMENIS, INC.·Product code GEX·March 17, 2004