3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TOTAL ASR ACET IMP SIZE 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·May 28, 2014
LEAD MODEL 304
FDA Adverse Event
Injury
·CYBERONICS INC·Product code LYJ·November 15, 2012
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code NIQ·September 14, 2010