BEUDAMED
    208 results · 33ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Other ×

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·February 21, 2007

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·February 20, 2007

    EPILIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·January 8, 2007

    INFRATOME 30 DEGREE

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·September 11, 2006

    LUMENIS ONE

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·March 13, 2007

    VASCULIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·March 9, 2007

    VASCULIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·March 9, 2007

    LIGHTSHEER

    FDA Adverse Event
    Other ·LUMENIS (SANTA CLARA)·Product code GEX·December 2, 2005

    DUOTOME 550

    FDA Adverse Event
    Other ·LUMENIS LTD.·Product code LNK·February 13, 2007

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·May 9, 2007

    LIGHTSHEER XC EXTENDED PULSE

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·January 3, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·RH-USA·Product code GEX·July 26, 2006

    VERSAPULSE VPW-110V

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·March 6, 2007

    SLIMLINE 365

    FDA Adverse Event
    Other ·LUMENIS LTD.·Product code GEX·March 15, 2007

    VASCULIGHT

    FDA Adverse Event
    Other ·LUMENIS LTD·Product code GEX·April 30, 2007

    LUMENIS

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·March 15, 2007

    SPECTRA, INTEGRATED

    FDA Adverse Event
    Other ·LUMENIS·Product code HQF·June 7, 2006

    LUMENIS 1

    FDA Adverse Event
    Other ·LUMENIS, LTD.·Product code GEX·February 20, 2007

    LIGHTSHEER (ALL MODELS)

    FDA Adverse Event
    Other ·LUMENIS, INC.·Product code GEX·May 8, 2007

    SURGICAL FIBER

    FDA Adverse Event
    Other ·LUMENIS·Product code GEX·April 28, 2006