3 results
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23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TRILOGY 202
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·April 4, 2013
CARPENTIER-EDWARDS PARIMOUNT MAGNA AORTIC BIOPROSTHESIS
FDA Adverse Event
Death
·EDWARDS LIFESCIENCES·Product code LWR·May 21, 2008
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·April 1, 2011