BEUDAMED
    32 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Death ×

    VERSAPULSE POWERSUITE 20W

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

    LX-20 / LX-20SP

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

    VERSAPULSE DUAL 80/100

    FDA Adverse Event
    Death ·COHERENT MEDICAL GROUP·Product code GEX·October 11, 2005

    LUMENIS VERSACUT TISSUE MORCELLATOR SYSTEM

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

    SURGICAL FIBER

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

    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

    SLIMLINE 1000

    FDA Adverse Event
    Death ·*·Product code GEX·May 8, 2006

    VALIANT THORACIC STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·November 13, 2012

    VERSACUT TISSUE MORCELLATOR

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

    HEARTMATE II LVAS

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·March 5, 2012

    SLIMLINE 200

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

    COHERENT

    FDA Adverse Event
    Death ·LUMENIS, INC·Product code LNK·October 17, 2005

    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

    PULSE

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

    SLIMLINE 200

    FDA Adverse Event
    Death ·LUMENIS (ISRAEL)·Product code LNK·August 12, 2005

    LUMENIS SLIMLINE 200 FOR COHERENT 200

    FDA Adverse Event
    Death ·LUMENIS, INC.·Product code MVF·July 18, 2005

    QUANTUM PSV

    FDA Adverse Event
    Death ·RESPIRONICS·Product code MNS·September 17, 1999

    INTRA AORTIC BALLOON

    FDA Adverse Event
    Death ·DATASCOPE CORP.·Product code DSP·August 19, 2014