BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 2 ×

    ShurFit Lumbar Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    VITEK 2 STRPTOCOCCUS AMPICILLIN

    FDA 510(k)
    FDA Class 2 ·Microbiology

    IMMULITE TOXOPLASMA IGM, MODEL LKTM1 AND LKTM2, IMMULITE 2000 TOXOPLASMA IGM, MODEL L2KTM2 AND L2KTM6

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Intervertebral Fusion Device With Bone Graft, Lumbar

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

    Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

    FDA classification
    FDA Class 2 ·Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

    System, Test, Automated, Antimicrobial Susceptibility, Short Incubation

    FDA classification
    FDA Class 2 ·System, Test, Automated, Antimicrobial Susceptibility, Short Incubation