6 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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RMI CAROTID BY-PASS SHUNT
FDA 510(k)
FDA Class 2
·Cardiovascular
Biopor, AOC Porous Polyethylene, Cerepor
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
TOTAL AND HEMI SHOULDER SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
FDA classification
FDA Class 2
·Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
FDA classification
FDA Class 2
·Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
FDA classification
FDA Class 2
·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented