16 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
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