20 results · 25ms · Sources: EU EUDAMED, US FDA

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PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 9, 2016

ADAPTA DR

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

ADAPTA D

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·June 10, 2015

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2015

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code NVZ·March 27, 2015

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code NVZ·May 1, 2018

MEDTRONIC LEAD

FDA Adverse Event
Injury ·MEDTRONIC, PLC·Product code DXY·March 27, 2015

REVEAL XT

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DSI·August 9, 2016

ENRHYTHM

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code NVZ·December 23, 2014

PULSE GENERATOR, PERMANENT, IMPLANTABLE

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code NVZ·December 22, 2016

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·February 16, 2016

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Death ·MEDTRONIC, INC.·Product code DXY·February 23, 2016

VIRTUOSO DR

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code LWS·February 10, 2015

PULSE-GENERATOR, PACEMAKER, IMPLANTABLE

FDA Adverse Event
Injury ·MEDTRONIC, INC.·Product code DXY·June 9, 2016

LOCK BIPOL.SELF-CENT.HEAD 49

FDA Adverse Event
Injury ·LIMACORPORATE SPA·Product code LPH·July 15, 2020

ITREL

FDA Adverse Event
MEDTRONIC, INC.·Product code GZB·February 18, 2000

LIBERTY CYCLER

FDA Adverse Event
Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FKX·June 25, 2014

EON MINI

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·February 22, 2013

TERUMO ADVANCED PERFUSION SYSTEM 1

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DTQ·January 24, 2011