89 results · 49ms · Sources: EU EUDAMED, US FDA

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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