3 results
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42ms
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Sources: EU EUDAMED, US FDA
Filters
FDA Classification
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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