7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAPIOX CARDIOPLEGIA
FDA 510(k)
FDA Class 2
·Cardiovascular
Simplexa GBS Direct, Simplexa GBS Positive Control Pack
FDA 510(k)
FDA Class 1
·Microbiology
ENSITE FUSION DYNAMIC REGISTRATION TOOL
FDA 510(k)
FDA Class 2
·Cardiovascular
SUPRACONDYLAR NAIL T2 SCN 10 X 200 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS ¿ KIEL·Product code HSB·July 17, 2012
CONSTELLATION VISION SYSTEM
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·February 26, 2013
UNICEL® DXI 800 ACCESS IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LFX·February 9, 2011
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·August 6, 2014