10,000 results
·
134ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ATTAIN COMMAND 6250 LEFT HEART DELIVERY SYSTEMS AND GUIDE CATHETERS FOR LEFT HEART DELIVERY
FDA 510(k)
FDA Class 2
·Cardiovascular
Attain Select II + SureValve delivery catheter system, Attain Command + SureValve Left Heart Delivery System, Attain Comman + SureValve Guide Catheters for Left Heart Delivery, C315 Delivery Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
ATTAIN LDS 6216A LEFT HEART DELIVERY SYSTEM, ATTAIN ACCESS 6218A LEFT HEART DELIVERY SYSTEM, ATTAIN 6216A AND 6218A GUID
FDA 510(k)
FDA Class 2
·Cardiovascular
ATTAIN COMMAND 6250 LEFT HEART DELIVERY SYSTEMS AND ATTAIN COMMAND 6250 GUIDE CATHETERS FOR LEFT HEART DELIVERY
FDA 510(k)
FDA Class 2
·Cardiovascular
ATTAIN COMMAND+SUREVALVE LEFT HEART DELIVERY SYSTEM ATTAIN COMMAND GUIDE CATHETERS FOR LEFT HEART DELIVERY,ATTAIN SELECT
FDA 510(k)
FDA Class 2
·Cardiovascular
ION¿
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·March 22, 2012
LOTUS EDGE VALVE
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NPT·June 24, 2020
RADIUS CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code MAF·May 31, 2005
RADIUS CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code MAF·May 31, 2005
RADIUS CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code MAF·May 31, 2005
ACS RX MULTI-LINK CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·GUIDANT ACS/DVI·Product code MAF·June 18, 1998
RACER BILIARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC VASCULAR·Product code FGE·June 28, 2006
HI-TORQUE BALANCE GUIDE WIRE
FDA Adverse Event
Malfunction
·ACS/DVI·Product code DQX·March 27, 1997
NAVIFLEX RX DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·January 31, 2024
LIBRETE' MONORAIL CORONARY STENT DELIVERY SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORP.·Product code MAF·February 2, 2007
ACS RX MULTI-LINK HP CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·GUIDANT VASCULAR INTERVENTION·Product code MAF·February 4, 1999
ACS MULTILINK HP 35X15
FDA Adverse Event
Malfunction
·GUIDANT CORP.·Product code MAF·February 4, 1999
HI-TORQUE BALANCE GUIDE WIRE WITH HYDROCOAT
FDA Adverse Event
Malfunction
·GUIDANT VASCULAR INTERVENTION·Product code DQX·April 2, 2002
NAVIFLEX? RX DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code FGE·February 24, 2026
SMART CONTROL NITINOL STENT SYSTEM
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code FGE·September 28, 2012