3 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
TELIGEN IS-1/DF-1 - VR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS, INC·Product code LWS·November 11, 2008
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES·Product code MIH·September 14, 2011
ULTAMET MTL INS NEUT 28MM 50OD
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. ¿ REG. # 8010379·Product code KWA·July 30, 2013