3 results
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40ms
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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
System, Perfusion, Kidney
FDA classification
FDA Class 2
·System, Perfusion, Kidney
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)