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

    Shadow Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Meridian Anterior Plate System, Regatta Lateral Plate System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    QUANTA LITE GP210 ELISA

    FDA 510(k)
    FDA Class 2 ·Immunology

    Autoantibodies, Nuclear Pore Glycoprotein Gp210

    FDA classification
    FDA Class 2 ·Autoantibodies, Nuclear Pore Glycoprotein Gp210

    Catheter, Percutaneous

    FDA classification
    FDA Class 2 ·Catheter, Percutaneous

    Appliance, Fixation, Spinal Intervertebral Body

    FDA classification
    FDA Class 2 ·Appliance, Fixation, Spinal Intervertebral Body