10,000 results
·
128ms
·
Sources: EU EUDAMED, US FDA
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·Blazer Open Irrigated Cardiac Ablation System
Catheter, Percutaneous Transluminal Coronary Angioplasty (Ptca), Cutting/Scoring
FDA Pre-Market Approval
FDA Class 3
·Wolverine Coronary Cutting Balloon (Monorail and Over-The-Wire)
Stent, Renal
FDA Pre-Market Approval
FDA Class 3
·Express SD Monorail Premounted Stent System
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·Rebel Platinum Chromium Coronary Stent System (Monorail and Over-the-Wire)
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·Promus Premier Everolimus-Eluting Platinum Chromium Coronary Stent System
Glue, Surgical, Arteries
FDA Pre-Market Approval
FDA Class 3
·BIOGLUE SURGICAL ADHESIVE
Catheter, Coronary, Atherectomy
FDA Pre-Market Approval
FDA Class 3
·Rotablator Rotational Atherectomy System
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·REBEL Platinum Chromium Coronary Stent System
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·Blazer II XP Cardiac Ablation Catheter and Cable
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
FDA Pre-Market Approval
FDA Class 3
·Blazer Open Irrigated Temperature Ablation Catheter
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·Blazer II Cardiac Ablation Catheter and Cable
Stent, Renal
FDA Pre-Market Approval
FDA Class 3
·Express SD Monorail Premounted Stent System
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·Chilli II Cooled Ablation Catheter and Cable
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·PROMUS Elemen Plus Everolimus-Eiuting Stent System/ PROMUS PREMIER Everolimus-Eiuting Platinum Chromium Coronary Stent S
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·EBI OsteoGen Implantable Bone Growth Stimulators
Stimulator, Invasive Bone Growth
FDA Pre-Market Approval
FDA Class 3
·SpF Implantable Spinal Fusion Stimulators
RDA-XS
FDA registration
Ritter Implants GmbH & Co. KG·1 product·🇩🇪 Germany
Monaco
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Optos plc·1 device
Arm rest
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Optos plc·1 device
Nexstim NBS System 6
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Nexstim Plc·1 device