10,000 results
·
28ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
×
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·CHILLI II COOLED ABLATION CATHETER
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·STARCLOSE VASCULAR CLOSURE SYSTEM
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·SJM ICD'S PHOTON MICRO, EPIC, EPIC +, ATLAS, ATLAS + (ICDS)
Lens, Intraocular, Accommodative
FDA Pre-Market Approval
FDA Class 3
·CRYSTALENS MODEL AT-45 ACCOMMODATING INTRAOCULAR LENS (IOL)
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·THORATEC VENTRICULAR (VAD) ASSIST DEVICE SYSTEM
Ventricular (Assist) Bypass
FDA Pre-Market Approval
FDA Class 3
·HEARTMATE II LEFT VENTRICULAR ASSIST SYSTEM (LVAS)
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·PROMOTE Q/PROMOTE QUADRA/UNIFY QUADRA/QUARTET CRT-DS
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·ASCENDRA + DELIVERY SYSTEM
Lens, Multifocal Intraocular
FDA Pre-Market Approval
FDA Class 3
·SOFT ACRYLIC MULTIFOCAL ARRAY 2 (MODELS AA40E AND AA50) AND REZOOM (MODEL NXG1) INTRAOCULAR LENSES
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·QUICK-CLOSE VASCULAR SUTURING SYSTEM
Sensor, Glucose, Invasive
FDA Pre-Market Approval
FDA Class 3
·CARELINK PERSONAL SOFTWARE
Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·THE HANCOCK VALVED CONDUIT MODIFIED ORIFICE (MODEL 105)
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·VOYAGER OTW CORONARY DILATATION CATHETER
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE V AND PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEMS (EECSS)
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·HANCOCK PORCINE BIOPROSTHESIS
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·SUTURE MEDIATED CLOSURE SYSTEMS & ASSOCIATED ACCESSORIES
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·THERAPY ABLATION CATHETERS
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·Carpentier-Edwards PERIMOUNT Magna Pericardial Aortic Bioprosthesis 3000, with ThermaFix tissue process 3000TFX,Ease Per
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Precision Montage MRI Spinal Cord Stimulator System
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CADENCE FAMILY OF DEVICES