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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