8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DAIG PERCUTANEOUS CATHETER INTRO. & REMOVABLE HEMO
FDA 510(k)
FDA Class 2
·Cardiovascular
FAST-CATH¿ HEMOSTASIS INTRODUCER, CATH-LOCK¿ LOCKING HUB, 12 CM SHEATH, 8.5 F
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DYB·January 22, 2024
Arthrex®
FDA UDI
ARTHREX, INC.·00888867052505·DRILL GUIDE, 3.5MM, LOCKING
COMFEEL POWDER
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
TOP SINGLE USE U.T.W. A-V FISTULA NEEDLE Y TYPE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
GEMSTAR PAIN MGE SNG
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD·Product code FRN·April 23, 2014
SPEEDBAND SUPERVIEW SUPER 7, MODELS 4204
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - SPENCER·Product code MND·November 9, 2010
SERVO-I
FDA Adverse Event
Malfunction
·MAQUET CRITICAL CARE AB·Product code CBK·December 21, 2012