Aortic stent grafts
Autoinjector 2
A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is made of a metallic mesh structure with a polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.
Autoinjector 2 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 |
|---|---|---|---|
| TV-AI01-N | — | MR Conditional | Available |
| TV-AI01-N | — | MR Conditional | Available |
FDA clearances
- PMA P120006 August 2013
Procedures that use aortic stent grafts
Frequently asked questions
What is Autoinjector 2 used for?
A non-bioabsorbable tubular device typically implanted at the junction of the abdominal aorta and the common iliac arteries to reduce pressure on an abdominal aortic aneurysm (AAA) [includes aortoiliac aneurysm]; it does not contain anticoagulants or pharmaceuticals. It is percutaneously inserted via the femoral artery to the site of implantation where it self-expands. It is made of a metallic mesh structure with a polymer tube (endovascular graft) and is typically available as a: 1) single tube for insertion into the aorta and/or one iliac artery; or 2) two-part bifurcation design (e.g., Y-shaped tube) for insertion through both iliac arteries.
Who makes Autoinjector 2?
Autoinjector 2 is made by Endologix LLC. It is listed under aortic stent grafts (evar/tevar) in our device library.
What sizes does Autoinjector 2 come in?
The FDA device database does not list sizes for Autoinjector 2. Check the instructions for use or ask a Endologix LLC representative.
Is Autoinjector 2 MRI safe?
The FDA device database lists Autoinjector 2 as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Autoinjector 2 FDA cleared?
Autoinjector 2 is covered by FDA submission P120006.
How do I contact a Endologix LLC sales representative?
Endologix LLC has not listed representatives on LA Vascular yet. Visit the Endologix LLC 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.