3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PROMUS PREMIER?
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·June 2, 2014
TOTAL ASR FEM IMP SIZE 53
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·November 23, 2012
CONTINUOUS WAVE III ARTHROSCOPY PUMP
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code HRX·September 24, 2010