7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
UNIVENT TUBE 7.0MM, 7.5MM, 8.0MM, 8.5MM, 9.0MM
FDA 510(k)
FDA Class 2
·Anesthesiology
Arthrex®
FDA UDI
ARTHREX, INC.·00888867052444·ATTACHMENT SCREW, AIMING GUIDE
URIHESIVE SYSTEM - IMPROVED
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
X-RAY TUBESTANDS BUCKY STANDS & VETERINARY X-RAY
FDA 510(k)
FDA Class 1
·Radiology
GEMSTR 7 THPY ALT ST
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·April 23, 2014
ENDO GIA ROTICULATOR 60-3.5 SULU
FDA Adverse Event
Injury
·UNITED STATES SURGICAL·Product code GDW·November 1, 2010
RELIEVA FLEX SINUS GUIDE CATHETER
FDA Adverse Event
Malfunction
·ACCLARENT·Product code LRC·November 16, 2012