10,000 results
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40ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ATHEROCATH-GTO
FDA Adverse Event
Malfunction
·DEVICES FOR VASCULAR INTERVENTION, INC.·Product code MCX·May 25, 1995
SYNCHROMED II
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·August 22, 2014
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code MCX·January 12, 2001
ATHEROCATH-GTO, 7 FR
FDA Adverse Event
Malfunction
·DEVICES FOR VASCULAR INTERVENTION·Product code MCX·December 27, 1994
ATHEROCATH-GTO ATHERECOMY DEVICE
FDA Adverse Event
Malfunction
·GUIDANT ACS/DVI·Product code MCX·October 24, 1997
TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿ BID CURVE D-F
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code OAE·December 18, 2023
TACTICATH¿ CONTACT FORCE ABLATION CATHETER, SENSOR ENABLED¿ BID CURVE D-F
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code OAE·December 18, 2023
PTCA WIRE
FDA Adverse Event
Injury
·CORDIS·Product code DQX·July 6, 1995
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code MCX·July 12, 2000
DYNASTY® BF SHELL 60MM GROUP G
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code KWA·October 16, 2018
DYNASTY® A-CLASS® 15DG POLY
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code LPH·October 16, 2018
COCR TRANSCEND® FEMORAL HEAD
FDA Adverse Event
Injury
·MICROPORT ORTHOPEDICS INC.·Product code JDL·October 16, 2018
RESERVOIR 1.8ML MMT-326A
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 18, 2018
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Malfunction
·DEVICES FOR VASCULAR INTERVENTION, INC.·Product code MCX·September 30, 1996
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code MCX·December 22, 2000
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code MCX·December 7, 2000
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code MCX·December 19, 2000
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Malfunction
·ACS/DVI·Product code MCX·April 4, 1997
ATHEROCATH GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·GUIDANT ACS/DVI·Product code MCX·July 9, 1998
ATHEROCATH-GTO CORONARY ATHERECTOMY CATHETER
FDA Adverse Event
Injury
·ADVANCED CARDIOVASCULAR SYSTEMS, INC.·Product code MCX·November 8, 1996