BEUDAMED
    14 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    OMNIGUIDE BEAMPATH NEURO-L FIBER

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·April 15, 2010

    UNKNOWN

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·June 16, 2010

    OMNIGUIDE FIBER

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC·Product code GEX·December 14, 2017

    OMNIGUIDE BP 100 CO2 LASER FIBER

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·June 14, 2007

    YAG LASER

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC·Product code GEX·November 29, 2005

    OMNIGUIDE BEAMPATH CO2 MARK I LASER BEAM DELIV

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·November 26, 2005

    OMNIGUIDE LP 150

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·October 15, 2007

    BP-ROBOTIC

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·November 2, 2012

    OMNIGUIDE BEAMPATH ENT-L

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·September 3, 2009

    OMNIGUIDE BEAMPATH NEURO-L

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·August 12, 2009

    OMNIGUIDE BEAMPATH NEURO-L

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC·Product code GEX·August 12, 2009

    OMNIGUIDE LIGHTPATH 150

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·April 17, 2008

    OMNIGUIDE LP 150

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·March 11, 2008

    OMNIGUIDE LAPFLEX HANDPIECE

    FDA Adverse Event
    Injury ·OMNIGUIDE, INC.·Product code GEX·April 28, 2015