2,545 results
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31ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·EnVeo R, EnVeo PRO and Evolut PRO+ Delivery Catheter Systems
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DUETT PRO MODEL 1010 AND DIAGNOSTIC DUETT PRO MODEL 2210
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·DUETT PRO SEALING DEVICE AND DIAGNOSTIC DUETT PRO SEALING DEVICE
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·Evolut PRO+ Transcatheter Aortic Valves of the Evolut PRO+ System
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·Amplatzer PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO OCCLUDER
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·Evolut PRO+ Sysstem
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO OCCLUDER
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO OCCLUDER
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Infinion Pro Leads
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·Evolut PRO+ System
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO OCCLUDER
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·Amplatzer PFO Occluder
Transcatheter Septal Occluder
FDA Pre-Market Approval
FDA Class 3
·AMPLATZER PFO Occluder
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·AED Pro Device