3 results
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19ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ARTICULEZE M HEAD 36MM +1.5
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. ¿ REG. # 8010379·Product code JDI·May 6, 2014
EON PATIENT PROGRAMMER
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 10, 2012
SYBRONPRO TL
FDA Adverse Event
Injury
·EBI INC.·Product code DZE·August 10, 2010