3 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
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DEPUY ASR XL FEM IMP SIZE 51
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL LTD. 8010379·Product code KWA·February 15, 2013
DOUBLE FENESTRATED GRASPER INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·July 29, 2014
PRINEO SKIN CLOSURE SYSTEM
FDA Adverse Event
Injury
·ETHICON, INC.·Product code MPN·January 11, 2011