2,359 results
·
39ms
·
Sources: EU EUDAMED, US FDA
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Eluvia Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·ELUVIA Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·ELUVIA Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Eluvia Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Eluvia Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Eluvia Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·ZILVER PTX DRUG-ELUTING PERIPHERAL STENT
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Zilver® PTX® Peripheral Drug-Eluting Stent
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Zilver PTX Drug-Eluting Peripheral Stent
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Eluvia Drug-Eluting Vascular Stent System
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Zilver® PTX® Drug-Eluting Peripheral Stent
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Zilver PTX Drug-Eluting Peripheral Stent
Stent, Superficial Femoral Artery, Drug-Eluting
FDA Pre-Market Approval
FDA Class 3
·Zilver PTX Drug-Eluting Peripheral Stent
Control Material, Her-2/Neu, Immunohistochemistry
FDA classification
FDA Class 2
·Control Material, Her-2/Neu, Immunohistochemistry
PMMA BLOCK
FDA 510(k)
FDA Class 2
·Dental
Fluorescence Mode
FDA 510(k)
FDA Class 2
·Dental
PRIMUS
FDA 510(k)
FDA Class 2
·Ophthalmic
Disposable Medical Face Mask
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Yunnan Anpu Medical Technology Co., Ltd·1 device
System, Test, Her-2/Neu, Nucleic Acid Or Serum
FDA Pre-Market Approval
FDA Class 3
·HER2 IQFISH PHARMDX
System, Test, Her-2/Neu, Nucleic Acid Or Serum
FDA Pre-Market Approval
FDA Class 3
·HER2 FISH PHARMDX KIT