Keos Lumbar Instrument

FDA UDI

KEOS·B0842002000260·

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Abre™ Venous Self-expanding Stent System

FDA registration

Medtronic, Inc.·1 product·🇺🇸 United States

Medtronic2686 (MN) - Abre Venous Self-expanding Stent System

FDA registration

Isomedix Operations, Inc.·1 product·🇺🇸 United States

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre™ Venous Self-expanding Stent Systems Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous self-expanding stent system

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre™ Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre™ Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre™ Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre™ Venous Self-expanding Stent System

Stent, Iliac Vein

FDA Pre-Market Approval

FDA Class 3 ·Abre™ Venous Self-expanding Stent System

Curette, Suction, Endometrial (And Accessories)

FDA classification

FDA Class 2 ·Curette, Suction, Endometrial (And Accessories)

Stent, Iliac Vein

FDA classification

FDA Class 3 ·Stent, Iliac Vein

Indicator, Biological Sterilization Process

FDA classification

FDA Class 2 ·Indicator, Biological Sterilization Process