7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Arthrex 3.9 mm SwiveLock Anchor
FDA 510(k)
FDA Class 2
·Orthopedic
Vilex Guidewire
FDA UDI
VILEX IN TENNESSEE, INC.·00841731120700·Steinmann Pin 3.5x230mm (9/64 x 9")
VERSAPORT V2 BLADELESS OPTICAL TROCAR
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
BIOUNIVERSAL PKF
FDA 510(k)
FDA Class 2
·Dental
INTERSTIM II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·August 15, 2011
UV-FLASH SOLUTION TRANSFER SET(SHORT)-JAPAN
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code KDJ·November 17, 2008
PREFYX PPS SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - SPENCER·Product code FTL·July 16, 2013