25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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JOSTRA ARTERIAL PERFUSION CANNULAE
FDA 510(k)
FDA Class 2
·Cardiovascular
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021335040·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033441497·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033441527·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021335057·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021335590·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033441503·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00024021335026·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00031568335594·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00031568335020·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00031568335051·
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00031568335044·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033441510·
AVL HINGE KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HRH-63 HEAD ARRAY COIL
FDA 510(k)
FDA Class 2
·Radiology
BILATERAL DOUBLE BALLOON SET
FDA Adverse Event
Malfunction
·PAJUNK GMBH MEDIZINTECHNOLOGIE·Product code KOG·December 7, 2006
FEMOSTOP
FDA Adverse Event
Malfunction
·RADI MEDICAL SYSTEMS, INC.·Product code MGB·November 21, 2003
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·March 20, 2013
ASR UNI FEMORAL IMPL SIZE 47
FDA Adverse Event
Injury
·DEPUY INT'L LTD·Product code KWA·February 24, 2011
ACCU-CHEK COMFORT CURVE TEST STRIPS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·March 12, 2008