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·June 14, 2014
MAXPLUS CLEAR NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION CORPORATION·Product code FPA·November 15, 2012
PENUMBRA SYSTEM SEPARATOR 026
FDA Adverse Event
Malfunction
·PENUMBRA INC.·Product code NRY·September 17, 2010