3 results
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19ms
·
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 12, 2014
VIPER MIS CANNULATED SCREW 6X40MM, TI
FDA Adverse Event
Injury
·DEPUY SPINE INC.·Product code NKB·October 11, 2010
PINNACLE MTL INS NEUT36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code KWA·December 12, 2012