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

    Keos Anterior Cervical Interbody Fusion Device System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MHI-TM2000 LINEAR ACCELERATOR SYSTEM VERO IMAVIS

    FDA 510(k)
    FDA Class 2 ·Radiology

    DIAMEDIX IS-ANTI-CARDIOLIPIN IGA TEST SYSTEM

    FDA 510(k)
    FDA Class 2 ·Immunology

    Intervertebral Fusion Device With Bone Graft, Cervical

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

    System, Test, Anticardiolipin Immunological

    FDA classification
    FDA Class 2 ·System, Test, Anticardiolipin Immunological

    Accelerator, Linear, Medical

    FDA classification
    FDA Class 2 ·Accelerator, Linear, Medical