3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
COBLATOR II
FDA Adverse Event
Malfunction
·ARTHROCARE CORPORATION·Product code GEI·May 7, 2014
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 8, 2013
TRIAGE CARDIAC PANEL 25 TEST
FDA Adverse Event
Injury
·ALERE SAN DIEGO, INC·Product code NBC·November 12, 2010