3 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
U BY KOTEX SLEEK
FDA Adverse Event
Malfunction
·KIMBERLY-CLARK CORPORATION - CONWAY MILL·Product code HEB·April 24, 2014
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·October 4, 2012
SPYGLASS COMPONENT
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code KOG·July 28, 2010