55 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
×
ATLAS CONTROLLER
FDA Adverse Event
Injury
·ARTHROCARE CORPORATION·Product code GEI·November 30, 2009
TURBOVAC 90 ARTHROWAND
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·October 28, 2009
TURBOVAC 90 ARTHROWAND
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·October 28, 2009
TURBOVAC 90 ARTHROWAND
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·October 28, 2009
QUANTUM II SYSTEM
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 28, 2011
TOPAZ MICRODEBRIDER W / INTEGRATED FINGER SWITCH
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 28, 2011
TOPAZ MICRODEBRIDER W / INTEGRATED FINGER SWITCH
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 28, 2011
ARTHROCARE QUANTUM SYSTEM
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·April 22, 2009
SUPER TURBOVAC WITH INTEGRATED CABLE
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·April 22, 2009
TURBOVAC 90 WITH INTEGRATED CABLE
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 9, 2008
ARTHROCARE SYSTEM 2000
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 9, 2008
ARTHROCARE FOOT CONTROL
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 9, 2008
COBLATOR II SURGERY SYSTEM
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·October 28, 2011
EVAC 70 XTRA
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·October 28, 2011
DYONICS RF SYSTEM
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·November 10, 2011
ATLAS CONTROLLER
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·August 28, 2007
EVAC 70 XTRA WITH INTEGRATED CABLE
FDA Adverse Event
Injury
·ARTHROCARE CORPORATION·Product code GEI·June 9, 2010
EVAC 70 XTRA PLASMA WAND WITH INTEGRATED CABLE
FDA Adverse Event
Injury
·ARTHROCARE CORP·Product code GEI·June 28, 2011
SUPER TURBOVAC 90 WITH INTEGRATED CABLE
FDA Adverse Event
Injury
·ARTHROCARE CORP.·Product code GEI·September 17, 2010
COBLATOR II SYSTEM
FDA Adverse Event
Injury
·ARTHROCARE CORP·Product code GEI·June 28, 2011