6 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EIA KIT FOR THE DETCTION OF ANTI-PR3 ANTIBODIES
FDA 510(k)
FDA Class 2
·Immunology
V-TREND TARGET RF TEST
FDA 510(k)
FDA Class 2
·Immunology
Hive Standalone Cervical System and Hive C Interbody System
FDA 510(k)
FDA Class 2
·Orthopedic
*
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC·Product code MAF·February 3, 2013
FLEXTEND
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·January 10, 2011
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·July 23, 2014