16 results · 31ms · Sources: EU EUDAMED, US FDA

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STAT DL 9.5 FR. 40 CC. IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·January 28, 1998

SYNCHROMED II

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·May 8, 2014

PEAK PLASMABLADE TISSUE DISSECTION DEVICE

FDA Adverse Event
Malfunction ·MEDTRONIC ADVANCED ENERGY LLC·Product code GEI·October 17, 2012

ENDEAVOR SPRINT RX CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·August 11, 2010

INDUCTOS

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·July 25, 2012

MELODY TRANSCATHETER PULMONARY VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·January 23, 2019

FREESTYLE AORTIC ROOT BIOPROSTHESIS

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·January 23, 2019

HANCOCK

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·January 23, 2019

VALVE CONTEGRA

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code MWH·January 23, 2019

MELODY TRANSCATHETER PULMONARY VALVE

FDA Adverse Event
Malfunction ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·January 23, 2019

FILLER, RECOMBINANT HUMAN BONE MORPHOGENETIC P

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NEK·April 2, 2020

INDUCTOS

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code NEK·November 16, 2011

INTRASTENT MAX LD

FDA Adverse Event
Malfunction ·COVIDIEN·Product code FGE·January 25, 2019

INTRASTENT MAX LD

FDA Adverse Event
Injury ·COVIDIEN·Product code FGE·January 25, 2019

CD HORIZON SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·February 22, 2021

STAT DL 9.5 FR. 40 CC. IAB

FDA Adverse Event
Malfunction ·DATASCOPE CORP.·Product code DSP·January 28, 1998