6 results
·
18ms
·
Sources: EU EUDAMED, US FDA
IV CATHETER AND OBTURATOR
FDA 510(k)
FDA Class 2
·General Hospital
SORRENTO BONE GRAFT SUBSTITUTE
FDA 510(k)
FDA Class 2
·Orthopedic
ECHELON Synergy MRI System
FDA 510(k)
FDA Class 2
·Radiology
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SWINFORD·Product code KDI·February 4, 2013
KINETIX PTCA GUIDEWIRE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQX·December 29, 2010
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·July 17, 2014