2,511 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC)
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
Iliac Covered Stent, Arterial
FDA Pre-Market Approval
FDA Class 3
·GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis
Iliac Covered Stent, Arterial
FDA Pre-Market Approval
FDA Class 3
·GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·SM-1, CR-1, & GR-1 IOLS
System, Endovascular Graft, Aortic Aneurysm Treatment
FDA Pre-Market Approval
FDA Class 3
·GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC)
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·TactiCath Contact Force Ablation Catheter, Sensor Enabled
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI COOLED RF ABLATION SYSTEM
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·EP TECHNOLOGIES EPT-1000 XP RF ABLATION SYSTEM
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·PRECISION SPINAL CORD STIMULATOR (SCS) SYSTEM
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·HEARTWARE LEFT VENTRICULAR ASSIST SYSTEM
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·EP TECHNOLOGIES EPT-1000 XP RF ABLATION SYSTEM
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
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC(R) JEWEL(R) AF 7250 DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR, MODEL 9961 PROGRAMMER APPLICATION SOF
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·OmniaSecure MRI SureScan Lead Model 3930M
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CAPSURE LEAD
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSUREFIX LEAD, CAPSUREFIX NOVUS LEAD, SUREFIX LEAD, VITATRON CRYSTALLINE LEAD