8 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TRUEdraw Lancing Device, Mini Lancing Device
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Sklar®
FDA UDI
SKLAR CORPORATION·10649111319037·LISTER BANDAGE SCISS DEL 7 1/4
VASCULAR TECHNOLOGY INCORPORATED
FDA registration
VASCULAR TECHNOLOGY INCORPORATED·2 products·🇺🇸 United States
SOMATOM DEFINITION FLASH
FDA 510(k)
FDA Class 2
·Radiology
FILMSAVER, NT VERSION 5.03
FDA 510(k)
FDA Class 2
·Radiology
FORTIFY VR, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·November 3, 2014
GORE TEX VASCULAR GRAFT
FDA Adverse Event
Injury
·W.L. GORE & ASSOCIATES,INC·Product code DSY·July 2, 2013
DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·November 12, 2015