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

    LDR SPINE USA AVENUE L INTERBODY FUSION

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Intervertebral Fusion Device With Integrated Fixation, Lumbar

    FDA classification
    FDA Class 2 ·Intervertebral Fusion Device With Integrated Fixation, Lumbar

    RELISA MPO-ANCA TEST SYSTEM FOR ANTIBODIES TO MYELOPEROXIDASE, MODEL # 7096-15

    FDA 510(k)
    FDA Class 2 ·Immunology

    DIXTAL DZ-4100 SERIES PULSE OXIMETER

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

    FDA classification
    FDA Class 2 ·Test System, Antineutrophil Cytoplasmic Antibodies (Anca)

    Oximeter

    FDA classification
    FDA Class 2 ·Oximeter