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

    ARDIS INTERBODY SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MAGNETOM AERA AND MAGNETOM SKYRA

    FDA 510(k)
    FDA Class 2 ·Radiology

    GENESIS DM MODEL: 6053000A1

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Transmitters And Receivers, Physiological Signal, Radiofrequency

    FDA classification
    FDA Class 2 ·Transmitters And Receivers, Physiological Signal, Radiofrequency

    System, Nuclear Magnetic Resonance Imaging

    FDA classification
    FDA Class 2 ·System, Nuclear Magnetic Resonance Imaging