9 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MIC TRANSGASTRIC JEJUNAL TUBE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Ophthalmic Knife
FDA UDI
KATENA PRODUCTS, INC.·00841668101506·DIAMOND KERATOME 3.0MM ANGLED
POLAR PAD (STERILE)
FDA 510(k)
FDA Class 2
·Physical Medicine
CHIN WAFER
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ONYX, AVM
FDA Adverse Event
Injury
·IRVINE·Product code MFE·September 23, 2014
STOPCOCK MANIFOLD GANGS
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FMG·June 17, 2020
CLOSURE FAST
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY VNUS MEDICAL TECHNOLOGIES·Product code GEI·January 18, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 14, 2010
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FKX·July 10, 2014