3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT ULTRAMINI METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 26, 2013
SYNCHRON® LX RHEUMATOID FACTOR (RF REAGENT)
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code DHR·March 17, 2011
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS DE MEXICO·Product code NIQ·March 25, 2008