3 results
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35ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
PULSE GEN MODEL 103
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·November 14, 2008
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code JDI·August 18, 2011
AGILITY POST AUG TALAR SZ 3
FDA Adverse Event
Injury
·1818910 DEPUY ORTHOPAEDICS, INC.·Product code HSN·July 18, 2013