10,000 results
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49ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Shunt, Portosystemic, Endoprosthesis
FDA Pre-Market Approval
FDA Class 3
·GORE VIATORR TIPS ENDOPROSTHESIS
Pump, Infusion, Implanted, Programmable
FDA Pre-Market Approval
FDA Class 3
·SynchroMed Infusion System, Ascenda Intrathecal Catheters
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·PG ESSENTIO MRI SR, PG ESSENTIO MRI DR, PG PROPONENT MRI SR, PG PROPONENT MRI DR, PG ACCOLADE MRI SR, PG ACCOLADE MRI D
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·Edwards SAPIEN 3 Transcatheter Heart Valve
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Juvederm Injectable Gel Implants
Kit, Dna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·cobas HPV Test
Sealant, Polymerizing
FDA Pre-Market Approval
FDA Class 3
·Progel Pleural Air Leak Sealant
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·IMAGEREADY MR CONDITIONAL PACING SYSTEM AND INGEVITY PACE/SENSE LEAD
Stent, Iliac Vein
FDA Pre-Market Approval
FDA Class 3
·Zilver Vena® Venous Self-Expanding Stent
Aid, Surgical, Viscoelastic
FDA Pre-Market Approval
FDA Class 3
·BIOLON®
Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Ceramic/Metal, Cemented Or Uncemented
FDA Pre-Market Approval
FDA Class 3
·R3 Delta Ceramic Acetabular System
Stimulator, Spinal-Cord, Totally Implanted For Pain Relief
FDA Pre-Market Approval
FDA Class 3
·Restore, Itrel, and Synergy Spinal Cord Stimulation Systems, Pisces, Resume, Specify, and Vectris Spinal Cord Stimulatio
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·Adapta, Versa, Sensia, Astra S DR MRI IPG, Astra S SR MRI IPG,Astra XT DR MRI IPG, Astra XT SR MRI IPG, Attesta DR MRI I
Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Metal/Polymer, Mobile Bearing
FDA Pre-Market Approval
FDA Class 3
·LCS (R) Total Knee System
Automated External Defibrillators (Non-Wearable)
FDA Pre-Market Approval
FDA Class 3
·X Series, Propaq MD
Mycobacterium Tuberculosis, Cell Mediated Immune Response, Enzyme-Linked Immunospot Test
FDA Pre-Market Approval
FDA Class 3
·T-SPOT®.TB Test
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·CareLink SmartSync Device Manager Base, 24970A
Percutaneous Cardiac Ablation Catheter For Treatment Of Atrial Fibrillation With Irreversible Electroporation
FDA Pre-Market Approval
FDA Class 3
·FARAWAVE Pulsed Field Ablation Catheter
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV-ICD System
Wearable Automated External Defibrillator
FDA Pre-Market Approval
FDA Class 3
·WEARABLE CARDIOVERTER DEFIBRILLATOR (WCD) 2000 LIFEVEST