16 results · 21ms · Sources: EU EUDAMED, US FDA

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E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·July 30, 2014

PRODISC-L POLYETHYLENE INLAY

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code MJO·May 6, 2011

DIAMONDTEMP ABLATION SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC·Product code OAE·August 9, 2023

SEE H10

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·March 4, 2019

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·December 16, 2014

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·April 21, 2016

INTERSTIM

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·January 3, 2013

UNKNOWN CATHETER

FDA Adverse Event
Injury ·MEDTRONIC DOMINICANA·Product code JXG·December 17, 2025

TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿

FDA Adverse Event
Injury ·ST. JUDE MEDICAL·Product code OAE·May 4, 2023

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·April 21, 2016

EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code FDA·February 18, 2026

REPLACEMENT HEART VALVE

FDA Adverse Event
Injury ·EDWARDS LIFESCIENCES·Product code DYE·April 20, 2018

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·May 13, 2014

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIP·May 13, 2014

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·June 8, 2017

E-LUMINEXX VASCULAR STENT

FDA Adverse Event
Injury ·ANGIOMED GMBH & CO. MEDIZINTECHNIK KG·Product code NIO·November 11, 2015