3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2014
TRILOGY 200
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·October 31, 2012
PENUMBRA SYSTEM 5MAXACE REPERFUSION CATHETER
FDA Adverse Event
Injury
·PENUMBRA, INC.·Product code NRY·June 4, 2015