8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VENOUS RETURN CANNULA W/CUFF 91039
FDA 510(k)
FDA Class 2
·Cardiovascular
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209131181·
FLEXIBLE LIQUID LIGHT GUIDE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR
FDA 510(k)
FDA Class 2
·Orthopedic
RESERVOIR 1.8ML
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code FRN·June 6, 2014
VASO VIEW HEMOPRO
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·November 29, 2012
HEARTSTART MRX-EMS DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHILIPS HEALTHCARE·Product code MKJ·September 30, 2010
Custom Pack - with Introducer Kit, part number TVS4011NI(L
FDA Enforcement
Class II
·Terminated·Windstone Medical Packaging, Inc.·March 8, 2017