3 results
·
18ms
·
Sources: EU EUDAMED, US FDA
Filters
FDA Adverse Event
×
AORTIC FLEX
FDA Adverse Event
Injury
·MEDTRONIC ATS MEDICAL·Product code LWQ·April 30, 2014
VENTAK PRIZM 2
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 10, 2012
STENOSCOPE
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD. (GE PRIVATE)·Product code JAA·July 29, 2010