5,569 results · 35ms · Sources: EU EUDAMED, US FDA

Thoraflex™ Hybrid

FDA UDI
VASCUTEK LTD·05037881026787·Thoraflex Hybrid Plexus 4 Hybrid Stent Device

Thoraflex™ Hybrid

FDA UDI
VASCUTEK LTD·05037881026848·Thoraflex Hybrid Plexus 4 Hybrid Stent Device

Thoraflex™ Hybrid

FDA UDI
VASCUTEK LTD·05037881027005·Thoraflex Hybrid Ante-Flo Hybrid Stent Device

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA Pre-Market Approval
FDA Class 3 ·Thoraflex™ Hybrid

Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

FDA classification
FDA Class 3 ·Hybrid Stent Graft, Thoracic Aortic Lesion Treatment

Massage chair

FDA registration
FUAN AOSIKA ELECTRICAL TECHNOLOGY CO.,LTD·1 product·🇨🇳 China

COUNTERSINK

FDA registration
ORCHID UNIQUE·1 product·🇺🇸 United States

LSK-Wintrich GmbH

Manufacturer
🇩🇪 Germany

ASK-1 - Aspiration Starter Kit

FDA registration
Ranfac Corp.·1 product·🇺🇸 United States