3 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ELLIPSE DR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·February 28, 2013
UNKNOWN DEPUY 32+ 15 HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code JDI·January 28, 2011
EVIA HF-T
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code NKE·August 6, 2014