83 results · 19ms · Sources: EU EUDAMED, US FDA

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