Peripheral stents
Astron
by Biotronik AG
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Astron 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 |
|---|---|---|---|
| 7/30/72 | — | MR Conditional | Available |
| 7/30/130 | — | MR Conditional | Available |
| 7/40/72 | — | MR Conditional | Available |
| 7/40/130 | — | MR Conditional | Available |
| 7/60/72 | — | MR Conditional | Available |
| 7/60/130 | — | MR Conditional | Available |
| 7/80/72 | — | MR Conditional | Available |
| 7/80/130 | — | MR Conditional | Available |
| 8/30/72 | — | MR Conditional | Available |
| 8/30/130 | — | MR Conditional | Available |
| 8/40/72 | — | MR Conditional | Available |
| 8/40/130 | — | MR Conditional | Available |
| 8/60/72 | — | MR Conditional | Available |
| 8/60/130 | — | MR Conditional | Available |
| 8/80/72 | — | MR Conditional | Available |
| 8/80/130 | — | MR Conditional | Available |
| 9/30/72 | — | MR Conditional | Available |
| 9/30/130 | — | MR Conditional | Available |
| 9/40/72 | — | MR Conditional | Available |
| 9/40/130 | — | MR Conditional | Available |
| 9/60/72 | — | MR Conditional | Available |
| 9/60/130 | — | MR Conditional | Available |
| 9/80/72 | — | MR Conditional | Available |
| 9/80/130 | — | MR Conditional | Available |
| 10/40/72 | — | MR Conditional | Available |
| 10/60/72 | — | MR Conditional | Available |
| 10/80/72 | — | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is Astron used for?
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to indefinitely maintain patency and improve luminal diameter in patients with atherosclerotic disease, or following the recanalization of a total occlusion. It may additionally be intended to be implanted in an obstructed biliary duct; it is not dedicated to carotid artery implantation, and not intended for connection with an aortic stent. It is made entirely of metal [e.g., Nitinol alloy mesh structure] and typically implanted by a dedicated instrument where it self-expands upon release or is balloon expanded.
Who makes Astron?
Astron is made by Biotronik AG. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does Astron come in?
The FDA device database does not list sizes for Astron. Check the instructions for use or ask a Biotronik AG representative.
Is Astron MRI safe?
The FDA device database lists Astron as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Astron FDA cleared?
Astron is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Biotronik AG sales representative?
Biotronik AG has not listed representatives on LA Vascular yet. Visit the Biotronik AG 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.