3 results
·
33ms
·
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·May 25, 2014
ASR XL ANATOMIC HEAD SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·November 14, 2012
NOT APPLICABLE
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code JJE·September 10, 2010