6 results
·
17ms
·
Sources: EU EUDAMED, US FDA
REDO CENTRAL VENOUS CATHETER-NEONATE
FDA 510(k)
FDA Class 2
·General Hospital
INFRONT LUMBAR INTERBODY FUSION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
OTI ALUMINA CERAMIC FEMORAL HEAD SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code MDS·May 30, 2014
SUMMIT POR TAPER SZ5 STD OFF
FDA Adverse Event
Injury
·DEPUY WARSAW·Product code LPH·November 21, 2012
NEW LIGASURE 5MM
FDA Adverse Event
Malfunction
·COVIDIEN LP, (VALLEYLAB)·Product code GEI·September 15, 2010