16 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Status: Injury
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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