89 results
·
49ms
·
Sources: EU EUDAMED, US FDA
VITATRON DA+ T-SERIES DR
FDA Adverse Event
Malfunction
·VITATRON MEDICAL B.V.·Product code DXY·August 4, 2015
VITATRON DA+ T-SERIES DR
FDA Adverse Event
Malfunction
·VITATRON MEDICAL B.V.·Product code DXY·August 5, 2015
DA+ C SERIES SR
FDA Adverse Event
Death
·VITATRON MEDICAL B.V.·Product code DXY·January 18, 2012
VITA II D
FDA Adverse Event
Malfunction
·VITATRON MEDICAL B.V.·Product code DXY·June 10, 2014
SAPHIR II
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·February 9, 2010
VITA 2 DDDR
FDA Adverse Event
Malfunction
·VITATRON MEDICAL B.V.·Product code DXY·January 10, 2002
CLARITY DDDR
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·January 10, 2002
DIAMOND II
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·March 8, 2002
NONE
FDA Adverse Event
Death
·VITATRON MEDICAL B.V.·Product code DTF·November 7, 2003
DIAMOND II DR
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·July 11, 2000
VITA VVIR
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code LWR·July 11, 2000
6000023-2013-00008
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code NVY·February 15, 2013
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·February 9, 2013
DA+ T SERIES DR
FDA Adverse Event
Malfunction
·VITATRON MEDICAL B.V.·Product code DXY·February 9, 2013
VITATRON DA+ C-SERIES DR
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·February 9, 2013
SELECTION AFM
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·May 10, 2005
DIAMOND 3
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·May 10, 2005
JADE 3 SSI
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·February 8, 2014
RUBY 3
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·February 8, 2014
VITATRON DA+ T-SERIES DR
FDA Adverse Event
Injury
·VITATRON MEDICAL B.V.·Product code DXY·June 8, 2013