27 results
·
51ms
·
Sources: EU EUDAMED, US FDA
ELLMAN SURGITRON 4.0 DUAL RF S5
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code GEI·May 21, 2010
DENTO-SURGE
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL INC.·Product code EKZ·March 26, 2004
PELLEVE HANDPIECE
FDA Adverse Event
Malfunction
·ELLMAN INTERNATIONAL, INC.·Product code GEI·March 22, 2012
DENTO-SURG 90 FFP
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL INC.·Product code EKZ·July 17, 2000
ELLMAN SURGITRON EMC
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL INC.·Product code GEI·September 28, 2000
LLETZ LOOP
FDA Adverse Event
Other
·ELLMAN INTERNATIONAL INC.·Product code JOS·June 9, 2000
SURGITRON 120 IEC/SURGITRON 4.0 DUAL
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code GEI·December 11, 2008
SURGITRON FFPF EMC
FDA Adverse Event
Death
·ELLMAN INTERNATIONAL, INC.·Product code GEI·November 24, 2009
SURGITRON RADIOLASE
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code GEI·October 24, 2008
SURGITRON
FDA Adverse Event
Malfunction
·ELLMAN INTERNATIONAL, INC.·Product code GEN·March 6, 2003
EMPIRE MICROINCISION ELECTRODE
FDA Adverse Event
ELLMAN INTERNATIONAL, INC.·Product code GEI·July 25, 2011
SUB MUCOSAL UPP ELECTRODE
FDA Adverse Event
Other
·ELLMAN INTERNATIONAL INC·Product code GEI·August 29, 2002
SURGITRON
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code GEI·April 14, 2006
SURGITRON
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code GEI·April 13, 2006
ELLMAN ELECTRODE
FDA Adverse Event
Other
·ELLMAN INTERNATIONAL INC·Product code JOS·March 31, 2000
5MM DISPOSABLE BALL ELECTRODE
FDA Adverse Event
Other
·ELLMAN INTERNATIONAL INC.·Product code GEI·January 11, 2000
SURGITRON FFPF EMC
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code GEI·September 29, 2009
ELLMAN SURGITRON FFPF OPHTHALMOLOGY
FDA Adverse Event
Injury
·ELLMAN INTERNATIONAL, INC.·Product code BWA·July 2, 2007
ELLMAN IEC NEUTRAL PLATE
FDA Adverse Event
Malfunction
·ELLMAN INTERNATIONAL, INC.·Product code ODR·April 3, 2008
BIPOLAR TRIGGER-FLEX PROBE
FDA Adverse Event
Malfunction
·ELLMAN INTERNATIONAL, INC.·Product code GEI·February 26, 2009