76 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LFIT V40 FEMORAL HEAD COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450266083·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450136621·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060702·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060641·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060665·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060634·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060672·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060696·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060689·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060658·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060719·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060733·
READERS.COM
FDA UDI
FGX INTERNATIONAL INC.·00192304060726·
MODIFICATION TO ARTOSCAN M
FDA 510(k)
FDA Class 2
·Radiology
ZOLL M SERIES
FDA 510(k)
FDA Class 3
·Cardiovascular
JAW INS. BULLET NOSE GRASPER 5MM 310MM
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·January 13, 2015
ARCOS 18X150MM SPL TPR DIST HA
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016
ARCOS HA MODULAR REVISION SYSTEM CONE PROXIMAL BODY 60MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·December 7, 2016
MARYLAND GSP.FORCEPS FEN.5/310MM HF CON.
FDA Adverse Event
Malfunction
·AESCULAP AG & CO. KG·Product code GEI·February 19, 2014