5 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
OT VERIO FLEX METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 29, 2016
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC CARDIOVASCULAR GALWAY·Product code NIQ·November 5, 2008
LINOX SMART SD 60/16
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO, KG·Product code LWS·July 15, 2011
PINN MAR NEUT 28IDX48OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·July 12, 2013
MECTACER BIOLOX OPTION HEADS
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code LZO·October 7, 2025