9 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
XIENCE PRO¿ S
FDA Adverse Event
Death
·ABBOTT VASCULAR·Product code NIQ·August 19, 2025
XIENCE PRO¿ S
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR·Product code NIQ·August 19, 2025
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code NIQ·February 5, 2010
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·November 19, 2018
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 22, 2013
COROX OTW-S 85-BP
FDA Adverse Event
Injury
·BIOTRONIK SE & CO. KG·Product code OJX·August 27, 2014
INRATIO
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC.·Product code GJS·April 13, 2011
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Death
·ABBOTT VASCULAR - CARDIAC THERAPIES·Product code NIQ·April 2, 2010
XIENCE SIERRA¿
FDA Adverse Event
Malfunction
·ABBOTT VASCULAR INC.·Product code NIQ·February 10, 2025