4 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
NEXGEN ALL POLY PATELLA SIZE 32 MM DIA. STANDARD 8.5 MM THICKNESS
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code JWH·January 20, 2017
CARPENTIER-EDWARDS PERIMOUNT RSR PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·February 6, 2013
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·January 4, 2011
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD·Product code MCM·July 21, 2014