3 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PULSE GEN MODEL 104
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·June 30, 2014
DUROM US ACETABULAR COMPONENT 52/46 L
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code KWA·November 11, 2010
2.4MM LCP DISTAL RADIUS T-PLATE 3H HEAD/4H SHAFT
FDA Adverse Event
Injury
·SYNTHES USA·Product code HRS·January 8, 2013