BEUDAMED
    275 results · 21ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Ventricular (Assist) Bypass

    FDA Pre-Market Approval
    FDA Class 3 ·THORATEC VENTRICULAR ASSIST DEVICE (VAD)

    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(R) B/BR

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Senza Spinal Cord Stimulation (SCS) 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

    Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

    FDA Pre-Market Approval
    FDA Class 3 ·Senza Spinal Cord Stimulation (SCS) System

    Implantable Cardioverter Defibrillator (Non-Crt)

    FDA Pre-Market Approval
    FDA Class 3 ·MODEL 6836 Y CONNECTOR (AID B/BR)

    Catheter, Percutaneous, Long Term, Intraspinal

    FDA Pre-Market Approval
    FDA Class 3 ·DUPEN LONG TERM EPIDURAL CATHETER