6 results
·
21ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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Keos Lumbar IBFD
FDA 510(k)
FDA Class 2
·Orthopedic
AFFIITY CP CENTRIFUGAL BLOOD PUMP
FDA 510(k)
FDA Class 2
·Cardiovascular
BIOGRAPH 64 AND BIOGRAPH 40
FDA 510(k)
FDA Class 2
·Radiology
Intervertebral Fusion Device With Bone Graft, Lumbar
FDA classification
FDA Class 2
·Intervertebral Fusion Device With Bone Graft, Lumbar
Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
FDA classification
FDA Class 2
·Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
System, Tomography, Computed, Emission
FDA classification
FDA Class 2
·System, Tomography, Computed, Emission