3 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
XCISE LAPAROSCOPIC MORCELLATOR
FDA Adverse Event
Malfunction
·LINA MEDICAL, INC·Product code HET·January 17, 2013
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011
PULSE GEN MODEL 103
FDA Adverse Event
Injury
·CYBERONICS, INC.·Product code LYJ·July 23, 2014