7 results
·
27ms
·
Sources: EU EUDAMED, US FDA
HORIZON 9000
FDA 510(k)
FDA Class 2
·Cardiovascular
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00673978161211·BLADE X875-167 FIXED LONGITUDINAL 65MM
U.V. SUNLAMP 95UF-11
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DYNA SYSTEM
FDA 510(k)
FDA Class 1
·Dental
CAPSURE SENSE
FDA Adverse Event
Death
·MEDTRONIC SINGAPORE OPERATIONS·Product code DTB·June 16, 2014
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 13, 2012
INTEGRATED APD SET W/CASSETTE3-PRONG
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 19, 2010