3 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
EDGE CATHETER SYSTEM
FDA Adverse Event
Malfunction
·SUPERDIMENSION INC.·Product code JAK·May 13, 2014
ASR UNI FEMORAL IMPL SIZE 41
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 11, 2013
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·November 18, 2010