BEUDAMED
    6 results · 20ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    Toro-L Interbody Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DUET DRF

    FDA 510(k)
    FDA Class 2 ·Radiology

    AGILENT COMPONENT MONITORING SYSTEM, AGILENT V24/26, AGILENT BIS MODULE, MODEL M1175A/76A/77A,REV.L,M1205A,REV.L,M1034A

    FDA 510(k)
    FDA Class 2 ·Neurology

    Intervertebral Fusion Device With Bone Graft, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Bone Graft, Lumbar

    Index-Generating Electroencephalograph Software

    FDA classification
    FDA Class 2 ·Index-Generating Electroencephalograph Software

    System, X-Ray, Fluoroscopic, Image-Intensified

    FDA classification
    FDA Class 2 ·System, X-Ray, Fluoroscopic, Image-Intensified