3 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
UNKNOWN DEPUY AML FEMORAL HIP STEM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.1818910·Product code KXA·June 27, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 8, 2013
ISOLINE
FDA Adverse Event
Malfunction
·SORIN BIOMEDICA CRM S.R.L.·Product code MRM·November 16, 2010