4 results
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20ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
ROOT CANAL INSTRUMENT
FDA Adverse Event
Other
·MICRO-MEGA SA·Product code EKS·January 25, 2010
TI CERVICAL SPINE LOCKING PLATE/SMALL STATURE 40MM(32MM)
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code KWQ·February 22, 2013
PULSE GEN MODEL 103
FDA Adverse Event
Malfunction
·CYBERONICS INC·Product code LYJ·January 18, 2011
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·August 1, 2014