7 results
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28ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GRANT MODIF OF DEBAKEY ABDOM AORTA CLMP
FDA 510(k)
FDA Class 2
·Cardiovascular
Buxton BioMedical
FDA UDI
Buxton Biomedical Inc·B7687611690·Spinal Fusion Curette,str.,6
ENDOSSEOUS DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
DIFFUSION SYSTEM, SINGLE-BREATH (47404A)
FDA 510(k)
FDA Class 2
·Anesthesiology
14/16 LG TAPER M HEAD 36MM+11
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC. 1818910 ·Product code JDI·September 26, 2012
G2 FUKTER STSTEM - FEMORAL
FDA Adverse Event
Malfunction
·BARD PERIPHERAL VASCULAR, INC.·Product code DTK·December 31, 2013
CELL-DYN SAPPHIRE ANALYZER
FDA Adverse Event
Injury
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·July 19, 2010