284 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·EPT-1000 CARDIAC ABLATION SYSTEM
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·HeartWare HVAD 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