106 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Dissection Repair
FDA Pre-Market Approval
FDA Class 3
·Tack Endovascular System (4F, 1.5-4.5mm)
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·ESPRIT BTK Everolimus Eluting Bioresorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·Esprit BTK Everolimus Eluting Resorbable Scaffold System
Scaffold, Infrapopliteal, Absorbable
FDA Pre-Market Approval
FDA Class 3
·ESPRIT BTK Everolimus Eluting Bioresorbable Scaffold System
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune Gio
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune System
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune®
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens (LAL), Light Delivery Device (LDD) System
Endovascular System For Treatment Of Thoracoabdominal And Pararenal Aortic Lesions
FDA Pre-Market Approval
FDA Class 3
·GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery Device
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·NOVOTFF-100A SYSTEM