83 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Leadless Cardiac Resynchronization Therapy (Crt)
FDA Pre-Market Approval
FDA Class 3
·WiSE® (Wireless Stimulation of the Endocardium Technology) CRT System
Leadless Cardiac Resynchronization Therapy (Crt)
FDA Pre-Market Approval
FDA Class 3
·WiSE® (Wireless Stimulation of the Endocardium Technology) CRT System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AID(R) B/BR
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·TRIFECTA VALVE
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·BIOCOR/EPIC VALVE
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous self-expanding stent system
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·AID-B/BR AND VENTAK ICD
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Abre Venous Self-expanding Stent System
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·CARPENTIER-EDWARDS PERIMOUNT PERICARDIAL AORTIC BIOPROSTHESIS,THEON PERICARDIAL AORTIC BIOPROSTHESIS WITH THERMAFIX