15 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·May 19, 2020
CXDI CCS NE VER.1.40.2
FDA Adverse Event
Malfunction
·CANON, INC·Product code MQB·May 17, 2013
NC TREK CORONARY DILATATION CATHETER
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code LOX·July 5, 2011
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·August 27, 2008
CONTOUR NEXT
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·February 24, 2020
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 1, 2019
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 1, 2019
CONTOUR PLUS LINK 2.4
FDA Adverse Event
Malfunction
·ASCENSIA DIABETES CARE US INC.·Product code NBW·August 1, 2019
CONTOUR PLUS
FDA Adverse Event
Injury
·ASCENSIA DIABETES CARE US INC.·Product code NBW·February 26, 2021
PROMUS ELEMENT PLUS EVEROLIMUS-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM
FDA Adverse Event
Death
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·January 18, 2013
PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Death
·CORCYM S.R.L.·Product code LWR·April 10, 2025
PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·CORCYM S.R.L.·Product code LWR·February 25, 2025
PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Malfunction
·CORCYM S.R.L.·Product code LWR·March 27, 2025
PROMUS ELEMENT¿ PLUS
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·December 18, 2012
PERCEVAL PLUS SUTRUELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·CORCYM S.R.L.·Product code LWR·January 12, 2025