3 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
840 VENTILATOR
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY NELLCOR PURITAN BENNETT IRELAND·Product code CBK·May 22, 2014
MARYLAND BIPOLAR FORCEPS
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·November 29, 2012
DELTA CER HEAD 12/14 36MM +1.5
FDA Adverse Event
Injury
·DEPUY (IRELAND) 9616671·Product code MRA·June 17, 2015