BEUDAMED
    10 results · 30ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    LUMENIS VERSACUT TISSUE MORCELLATOR SYSTEM

    FDA Adverse Event
    Death ·LUMENIS, LTD·Product code GEX·December 11, 2016

    SLIMLINE 200

    FDA Adverse Event
    Death ·LUMENIS, LTD.·Product code LNK·November 7, 2003

    SURGICAL FIBER

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

    LX-20 / LX-20SP

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

    VERSACUT

    FDA Adverse Event
    Death ·LUMENIS LTD·Product code GCJ·March 20, 2024

    LUMENIS MOSES 550 D\F\L

    FDA Adverse Event
    Death ·LUMENIS LTD·Product code GEX·March 26, 2024

    VERSACUT TISSUE MORCELLATOR

    FDA Adverse Event
    Death ·LUMENIS LTD.·Product code GEI·March 17, 2019

    PULSE

    FDA Adverse Event
    Death ·LUMENIS LTD·Product code GEX·June 4, 2025

    VERSACUT+ TISSUE MORCELLATOR

    FDA Adverse Event
    Death ·LUMENIS, LTD.·Product code GCJ·March 17, 2015

    SURGICAL FIBER

    FDA Adverse Event
    Death ·LUMENIS LTD. YOKNEAM·Product code GEX·January 11, 2010