305 results · 22ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

PRECISE RX NITINOL STENT

FDA Adverse Event
Injury ·CORDIS DE MEXICO·Product code FGE·April 15, 2010

ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

FDA Adverse Event
Injury ·CODMAN AND SHURTLEFF, INC·Product code NJE·March 20, 2017

ENDURANT STENT GRAFT

FDA Adverse Event
Malfunction ·MEDTRONIC IRELAND·Product code MIH·October 6, 2021

STENT - VASCULAR RECONSTRUCTION

FDA Adverse Event
Injury ·MEDOS INTERNATIONAL SARL·Product code NJE·December 15, 2021

REFLEX CATHETER

FDA Adverse Event
Injury ·MICRO THERAPEUTICS, INC. DBA EV3·Product code DQY·April 8, 2026

AMPHIRION DEEP PTA BALLOON CATHETER

FDA Adverse Event
Injury ·MEDTRONIC MEXICO·Product code DQY·February 1, 2017

MARQUEE

FDA Adverse Event
Injury ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·January 2, 2025

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·December 24, 2019

TRAILBLAZER SUPPORT CATHETER

FDA Adverse Event
Injury ·COVIDIEN·Product code DQY·August 26, 2020

AMPHIRION DEEP PTA BALLOON CATHETER

FDA Adverse Event
Injury ·COVIDIEN·Product code DQY·August 26, 2020

TRAILBLAZER SUPPORT CATHETER

FDA Adverse Event
Injury ·COVIDIEN·Product code DQY·August 26, 2020

AMPHIRION DEEP PTA BALLOON CATHETER

FDA Adverse Event
Injury ·COVIDIEN·Product code DQY·August 26, 2020

AMPHIRION DEEP PTA BALLOON CATHETER

FDA Adverse Event
Injury ·INVATEC SPA·Product code DQY·February 1, 2017

TRAILBLAZER

FDA Adverse Event
Injury ·COVIDIEN·Product code DQY·February 1, 2017

TRAILBLAZER

FDA Adverse Event
Injury ·COVIDIEN·Product code DQY·February 1, 2017

AMPHIRION DEEP PTA BALLOON CATHETER

FDA Adverse Event
Injury ·MEDTRONIC MEXICO·Product code DQY·February 1, 2017

ENDURANT AAA STENT GRAFT SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·November 30, 2012

NEU_INS_STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 1, 2012

SOLETRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 2, 2012

NEU_INS_STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·August 1, 2012