8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MEDGRAPHICS EXERCISE CONSULT
FDA 510(k)
FDA Class 2
·Anesthesiology
Instrument Case
FDA UDI
KATENA PRODUCTS, INC.·00841668111048·INSTRUMENT CASE SMALL ALUMINUM
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150607·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 230mm
SOFTVUE
FDA 510(k)
FDA Class 2
·Radiology
INSIGHT MILLENNIUM III
FDA 510(k)
FDA Class 2
·Physical Medicine
INFUSE BONE GRAFT
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·January 18, 2013
NEXGEN FLUTED STEMMED TIBIAL BROACH
FDA Adverse Event
Malfunction
·ZIMMER INC·Product code JWH·November 9, 2010
QUICKFLEX XL LV LEAD
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 9, 2014