6 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REAGENT, FIREFLY #395
FDA 510(k)
FDA Class 2
·Hematology
Solitaire 2 Revascularization Device, Solitaire Platinum Revascularization Device (Solitaire Revascularization Device)
FDA 510(k)
FDA Class 2
·Neurology
SPECTROPHOTOMETER ANALYSIS SYS.
FDA 510(k)
FDA Class 1
·Clinical Chemistry
FORTIFY ST, DF-4 CONNECTOR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·April 30, 2014
LINEAR HIP
FDA Adverse Event
Malfunction
·ENCORE MEDICAL, L.P.·Product code LPH·October 5, 2012
MONOPTY DISPOSABLE CORE BIOPSY INSTRUMENT
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 16, 2015