Peripheral stents
Flair Endovascular Stent Graft
by Bard Peripheral Vascular, Inc.
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to maintain patency and improve luminal diameter, typically in patients with symptomatic peripheral vascular disease or following the recanalization of a total occlusion. It may be intended for implantation in an artery adjacent to the aorta (e.g., iliac, renal), however it is not a dedicated component of an aortoiliac stent-graft assembly; it may additionally be intended for venous implantation. It is a metallic mesh-like structure with a synthetic polymer tube (endovascular graft); it does not include pharmaceuticals.
Flair Endovascular Stent Graft 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 |
|---|---|---|---|
| FAF06030 | — | MR Conditional | Available |
| FAF06040 | — | MR Conditional | Available |
| FAF06050 | — | MR Conditional | Available |
| FAF06070 | — | MR Conditional | Available |
| FAF07030 | — | MR Conditional | Available |
| FAF07040 | — | MR Conditional | Available |
| FAF07050 | — | MR Conditional | Available |
| FAF07070 | — | MR Conditional | Available |
| FAF08030 | — | MR Conditional | Available |
| FAF08040 | — | MR Conditional | Available |
| FAF08050 | — | MR Conditional | Available |
| FAF08070 | — | MR Conditional | Available |
| FAF09030 | — | MR Conditional | Available |
| FAF09040 | — | MR Conditional | Available |
| FAF09050 | — | MR Conditional | Available |
| FAS06030 | — | MR Conditional | Available |
| FAS06040 | — | MR Conditional | Available |
| FAS06050 | — | MR Conditional | Available |
| FAS06070 | — | MR Conditional | Available |
| FAS07030 | — | MR Conditional | Available |
| FAS07040 | — | MR Conditional | Available |
| FAS07050 | — | MR Conditional | Available |
| FAS07070 | — | MR Conditional | Available |
| FAS08030 | — | MR Conditional | Available |
| FAS08040 | — | MR Conditional | Available |
| FAS08050 | — | MR Conditional | Available |
| FAS08070 | — | MR Conditional | Available |
| FAS09030 | — | MR Conditional | Available |
| FAS09040 | — | MR Conditional | Available |
| FAS09050 | — | MR Conditional | Available |
FDA clearances
- PMA P060002 October 2012
Procedures that use peripheral stents
Frequently asked questions
What is Flair Endovascular Stent Graft used for?
A non-bioabsorbable tubular device intended to be implanted in a peripheral artery (excludes aorta, coronary, pulmonary, and intracranial arteries) to maintain patency and improve luminal diameter, typically in patients with symptomatic peripheral vascular disease or following the recanalization of a total occlusion. It may be intended for implantation in an artery adjacent to the aorta (e.g., iliac, renal), however it is not a dedicated component of an aortoiliac stent-graft assembly; it may additionally be intended for venous implantation. It is a metallic mesh-like structure with a synthetic polymer tube (endovascular graft); it does not include pharmaceuticals.
Who makes Flair Endovascular Stent Graft?
Flair Endovascular Stent Graft is made by Bard Peripheral Vascular, Inc.. It is listed under peripheral artery stents and covered stents, dialysis access devices in our device library.
What sizes does Flair Endovascular Stent Graft come in?
The FDA device database does not list sizes for Flair Endovascular Stent Graft. Check the instructions for use or ask a Bard Peripheral Vascular, Inc. representative.
Is Flair Endovascular Stent Graft MRI safe?
The FDA device database lists Flair Endovascular Stent Graft as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Flair Endovascular Stent Graft FDA cleared?
Flair Endovascular Stent Graft is covered by FDA submission P060002.
How do I contact a Bard Peripheral Vascular, Inc. sales representative?
Bard Peripheral Vascular, Inc. has not listed representatives on LA Vascular yet. Visit the Bard Peripheral Vascular, 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.