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·April 8, 2013
VERSALOK PREPACKED ANCHOR WITH ORTHOCORD
FDA Adverse Event
Injury
·DEPUY MITEK·Product code MBI·March 30, 2011
VENTAK MINI IV+
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·May 8, 2008