3 results
·
21ms
·
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·July 15, 2015
THORACIC GRASPER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·January 14, 2013
SMITH & NEPHEW
FDA Adverse Event
Injury
·SMITH & NEPHEW ORTHOPAEDICS, INC.·Product code HWA·December 3, 2010