6 results
·
25ms
·
Sources: EU EUDAMED, US FDA
SENTINEL SYSTEMS
FDA 510(k)
FDA Class 2
·Cardiovascular
CODMAN DURAL GRAFT IMPLANT, MODELS 80-1471, 80-1472, 80-1473, 80-1474, 80-1475, 80-1476, 80-1477, 80-1478, 80-1480, 80-1
FDA 510(k)
FDA Class 2
·Neurology
Portable Dental X-Ray (AXR60 S); Portable Dental X-Ray (AXR65 S)
FDA 510(k)
FDA Class 2
·Dental
PRONTOSAN SOLUTION ROUND BOT. "WEST" 350ML
FDA Adverse Event
Injury
·B. BRAUN MEDICAL AG·Product code FRO·May 19, 2014
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·November 15, 2012
PRIMARY IV PLUM SET
FDA Adverse Event
Malfunction
·HOSPIRA WORLDWIDE·Product code FPA·August 20, 2010