BEUDAMED
    283 results · 18ms · Sources: EU EUDAMED, US FDA
    Filters Classification: FDA Class 3 ×

    Cardiac Ablation Percutaneous Catheter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 CARDIAC ABLATION SYSTEM

    Cardiac Ablation Percutaneous Catheter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 CARDIAC ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP RF ABLATION SYSTEM

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·INTERSECT ENT PROPEL MINI SINUS IMPLANT

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP CARDIAC ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP CARDIAC ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP RF ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP CARDIAC ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP CARDIAC ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP RF ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP CARDIAC ABLATION SYSTEM

    Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

    FDA Pre-Market Approval
    FDA Class 3 ·EPT-1000 XP RF ABLATION SYSTEMS

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PROPEL MINI SINUS IMPLANT

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Propel® Contour Sinus Implant

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Propel and Propel Mini Sinus Implants

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PROPEL MINI SINUS IMPLANT, 6011

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PROPEL MINI SINUS IMPLANT

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PROPEL SINUS, MINI SINUS IMPLANT.

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·Propel, Propel mini and Propel Contour Sinus Implants

    Drug-Eluting Sinus Stent

    FDA Pre-Market Approval
    FDA Class 3 ·PROPEL, PROPEL MINI and PROPEL CONTOUR