Thrombectomy devices
Artix MT
A device intended to be percutaneously introduced into the vasculature (coronary, peripheral and/or intracranial) through an appropriate intravascular catheter for the removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction; revascularization may also be achieved through thrombus reorientation. Also referred to as a stent retriever or clot retrieval catheter, it consists of an expanding, stent-like wire net connected to a pusher wire primarily intended to grip and remove the emboli/thrombi; it might include a guide-catheter dedicated to introduction of the wire-net. This is a single-use device.
Artix MT models and sizes
From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.
| Model / catalog no. | Size | MRI | Status |
|---|---|---|---|
| 32-101 | — | Not stated | Available |
| 32-103 / AS-01244 | — | Not stated | Available |
Procedures that use thrombectomy devices
Frequently asked questions
What is Artix MT used for?
A device intended to be percutaneously introduced into the vasculature (coronary, peripheral and/or intracranial) through an appropriate intravascular catheter for the removal of clotted blood (i.e., a thrombus or thromboembolus) or other formed elements causing vascular obstruction; revascularization may also be achieved through thrombus reorientation. Also referred to as a stent retriever or clot retrieval catheter, it consists of an expanding, stent-like wire net connected to a pusher wire primarily intended to grip and remove the emboli/thrombi; it might include a guide-catheter dedicated to introduction of the wire-net. This is a single-use device.
Who makes Artix MT?
Artix MT is made by Inari Medical, Inc.. It is listed under mechanical thrombectomy devices in our device library.
What sizes does Artix MT come in?
The FDA device database does not list sizes for Artix MT. Check the instructions for use or ask a Inari Medical, Inc. representative.
Is Artix MT MRI safe?
The FDA device database entry for Artix MT does not state its MRI safety status. Check the labeling before MRI.
Is Artix MT FDA cleared?
Artix MT is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Inari Medical, Inc. sales representative?
Inari Medical, Inc. has not listed representatives on LA Vascular yet. Visit the Inari Medical, Inc. company page for contact details.
Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.