73 results · 16ms · Sources: EU EUDAMED, US FDA

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·AB5000/BVS 5000 CIRCULATORY SUPPORT SYSTEM

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·ABIOMED(R) BVS 5000 BI-VENTRICULAR SUPPORT SYSTEM

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·BVS 5000 BI-VENTRICULAR SUPPORT SYSTEM

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·BVS 5000 BI-VENTRICULAR SUPPORT SYSTEM

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·ABIOMED BVS 5000 BI-VENTRICULAR SUPPORT SYSTEM

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·Absorb GTi Bioresorbable Vascular Scaffold (BVS) System

Ventricular (Assist) Bypass

FDA Pre-Market Approval
FDA Class 3 ·ABIOMED BVS 5000 BI-VENTRICULAR SUPPORT SYSTEM

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·Absorb GT1 Bioresorbable Vascular Scaffold (BVS) System

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·Absorb GT1 Bioresorbable Vascular Scaffold (BVS) System.

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·Absorb GT1 Bioresorbable Vascular Scaffold (BVS) System

Absorbable Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·ABSORB GT1 BIORESORBABLE VASCULAR SCAFFOLD (BVS) SYSTEM

Reherniation Reduction Device

FDA Pre-Market Approval
FDA Class 3 ·Barricaid® Annular Closure Device

Reherniation Reduction Device

FDA Pre-Market Approval
FDA Class 3 ·Barricaid Annular Closure Device

Embolization Agent, Vascular

FDA Pre-Market Approval
FDA Class 3 ·LAVA® Liquid Embolic System (LAVA LES)

Reherniation Reduction Device

FDA Pre-Market Approval
FDA Class 3 ·Barricaid® Annular Closure Device

Reherniation Reduction Device

FDA Pre-Market Approval
FDA Class 3 ·Barricaid Anular Closure Device