186 results · 29ms · 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.

KINETRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·June 24, 2013

NEU_INTERSTIM_INS

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code EZW·July 12, 2012

IMPLANTABLE INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·August 17, 2017

TALENT AAA

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 1, 2014

ENDURANT

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 1, 2014

ANEURX

FDA Adverse Event
Injury ·MEDTRONIC CARDIOVASCULAR·Product code MIH·July 1, 2014

EXTERNAL NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·February 5, 2024

IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·December 13, 2022

COAGUCHEK XS SYSTEM

FDA Adverse Event
Injury ·ROCHE DIAGNOSTICS·Product code GJS·March 16, 2021

PANCREATIC STENT

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGE·February 10, 2022

EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·February 10, 2022

EVIS EXERA II DUODENOVIDEOSCOPE

FDA Adverse Event
Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·February 10, 2022

AMPLATZER SEPTAL OCCLUDER

FDA Adverse Event
Injury ·AGA MEDICAL CORPORATION·Product code MLV·December 24, 2017

ENDOTAK RELIANCE

FDA Adverse Event
Injury ·CPI - DEL CARIBE·Product code NVY·April 15, 2011

STRATA NSC LUMBOPERITONEAL SHUNT KIT

FDA Adverse Event
Injury ·MEDTRONIC NEUROSURGERY·Product code JXG·April 22, 2020

UNKNOWN IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·July 24, 2014

VISUALASE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC NAVIGATION, INC·Product code GEX·August 16, 2022

EVIS EXERA III BRONCHOVIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·December 12, 2024

EVIS EXERA III BRONCHOVIDEOSCOPE

FDA Adverse Event
Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·December 12, 2024

HEARTMATE 3 LEFT VENTRICULAR ASSIST SYSTEM

FDA Adverse Event
Injury ·THORATEC CORPORATION·Product code DSQ·December 9, 2021