8 results
·
18ms
·
Sources: EU EUDAMED, US FDA
RMHS MONOLITHIC FEMORAL COMPONENT
FDA 510(k)
FDA Class 2
·Orthopedic
Brigade
FDA UDI
Nuvasive, Inc.·00887517391421·CoRoent XLR-F, 16x42x30mm 12°
Brigade
FDA UDI
Nuvasive, Inc.·00887517192325·Brigade Trial, 16x42x30mm 12°
RSH BILIARY STONE REMOVAL DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Veuron-Brain-pAb3
FDA 510(k)
FDA Class 2
·Radiology
IN TOUCH ZU
FDA Adverse Event
Malfunction
·STRYKER MEDICAL-KALAMAZOO·Product code FNL·January 28, 2013
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Malfunction
·CORDIS DE MEXICO·Product code NIQ·December 17, 2010
GREENLIGHT XPS LASER SYSTEM
FDA Adverse Event
Malfunction
·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·July 14, 2014