BEUDAMED
    163 results · 24ms · Sources: EU EUDAMED, US FDA

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    PROCISE EZ PLASMA WAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·October 12, 2007

    PROCISE EZ PLASMA WAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·October 12, 2007

    PROCISE EZ PLASMA WAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·October 12, 2007

    PROCISE EZ PLASMA WAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·October 12, 2007

    ATLAS CONTROLLER

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code GEI·November 30, 2009

    COBLATOR II SYSTEM

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·April 29, 2011

    COBLATOR II SYSTEM

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·April 29, 2011

    QUANTUM II SYSTEM

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·October 21, 2011

    MULTIVAC XL ARTHROWAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·May 1, 2009

    MULTIVAC XL ARTHROWAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·May 1, 2009

    MULTIVAC XL ARTHROWAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·May 1, 2009

    AMBIENT SUPER TURBOVAC 90 WITH FINGER SWITCH

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·October 21, 2011

    AMBIENT SUPER TURBOVAC 90 WITH FINGER SWITCH

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORP.·Product code GEI·October 21, 2011

    ULTRAVAC WITH INTEGRATED CABLE

    FDA Adverse Event
    Other ·ARTHROCARE CORPORATION·Product code GEI·March 5, 2008

    MULTIVAC XL ARTHROWAND

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·May 11, 2009

    SUPER TURBOVAC 90 WITH INTEGRATED CABLE

    FDA Adverse Event
    Other ·ARTHROCARE CORP·Product code GEI·March 1, 2011

    PERC DC CONVENIENCE PACK

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·December 5, 2007

    ARTHROCARE PATIENT CABLE

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code HRX·December 18, 2007

    ATLAS CONTROLLER

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·December 28, 2007

    ATLAS SYSTEM

    FDA Adverse Event
    Other ·ARTHROCARE CORP.·Product code GEI·March 3, 2008