3,089 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Heart-Valve, Non-Allograft Tissue
FDA Pre-Market Approval
FDA Class 3
·Trifecta Valve with Glide Technology
Device, Angioplasty, Laser, Coronary
FDA Pre-Market Approval
FDA Class 3
·ELCA Coronary Atherectomy Catheters
Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring
FDA Pre-Market Approval
FDA Class 3
·Flextome Cutting Balloon Microsurgical Dilation Device
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·Portico
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·Navitor Transcatheter Aortic Heart Valve, Portico Transcatheter Aortic Heart Valve, FlexNav Delivery System
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·Myopore® Sutureless Myocardial Pacing Lead
Stimulator, Electrical, Implanted, For Parkinsonian Tremor
FDA Pre-Market Approval
FDA Class 3
·Brio Neurostimulation System
Dorsal Root Ganglion Stimulator For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Axium Neurostimulator System
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Genesis Neurostimulation System
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Level VIII Controlled Environment Area (CEA), Level IX CEA Dry Room
Kit, Assay, Progesterone Receptor
FDA Pre-Market Approval
FDA Class 3
·FLUORO-CEP (R) PROGESTERONE
Kit, Assay, Progesterone Receptor
FDA Pre-Market Approval
FDA Class 3
·FLUORO-CEP (R) PROGESTERONE
Kit, Assay, Progesterone Receptor
FDA Pre-Market Approval
FDA Class 3
·FLUORO-CEP (R) PROGESTERONE
Kit, Assay, Estrogen Receptor
FDA Pre-Market Approval
FDA Class 3
·FLUORO-CEP{R} ESTROGEN ASSAY REAGENT
Kit, Assay, Estrogen Receptor
FDA Pre-Market Approval
FDA Class 3
·FLUORO-CEP{R} ESTROGEN ASSAY REAGENT