7 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ENDOPEARL
FDA 510(k)
FDA Class 2
·Orthopedic
Polystar HK
FDA UDI
Merz Dental GmbH·D7091984171·anteriors; shade A3.5; mould 94
#875 DISPOSABLE BIOPOLAR CABLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SCIMED CARDIOTHERM CARDIOPLEGIA DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM
FDA Adverse Event
Injury
·CORDIS NEUROVASCULAR, INC.·Product code NJE·February 28, 2013
ACCU-CHEK ® COMPACT TEST DRUM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LFR·February 10, 2011
AL-III W/FOOT CONTROL
FDA Adverse Event
Malfunction
·DEPUY SYNTHES POWER TOOLS·Product code GEY·December 18, 2013