7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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REPAIR KIT QUINTON TRIPLE LUMEN RIGHT ATRIAL CATHE
FDA 510(k)
FDA Class 2
·Cardiovascular
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209124138·
NUCLIPASE (I125) PANCREATIC LIPASE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
TUCK-TITE COLON FLUID RETAINER
FDA 510(k)
FDA Class 1
·Gastroenterology, Urology
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·June 6, 2014
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·December 3, 2012
LOANER CORE IMPACTION DRILL
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code DZJ·September 7, 2010