3 results
·
26ms
·
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·June 6, 2014
PSI KIT: 8.5 FR X 4-1/8 (10 CM)
FDA Adverse Event
Malfunction
·ARROW INTL., INC.·Product code KGZ·November 14, 2012
INTEGRA
FDA Adverse Event
ROCHE DIAGNOSTICS·Product code JJE·September 30, 2010