Peripheral stents
LifeStream
by Clearstream Technologies Limited
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.
LifeStream 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 |
|---|---|---|---|
| LSMU0800516 | — | MR Conditional | Available |
| LSMU0800526 | — | MR Conditional | Available |
| LSMU0800537 | — | MR Conditional | Available |
| LSMU0800616 | — | MR Conditional | Available |
| LSMU0800626 | — | MR Conditional | Available |
| LSMU0800637 | — | MR Conditional | Available |
| LSMU0800658 | — | MR Conditional | Available |
| LSMU0800716 | — | MR Conditional | Available |
| LSMU0800726 | — | MR Conditional | Available |
| LSMU0800737 | — | MR Conditional | Available |
| LSMU0800758 | — | MR Conditional | Available |
| LSMU0800816 | — | MR Conditional | Available |
| LSMU0800826 | — | MR Conditional | Available |
| LSMU0800837 | — | MR Conditional | Available |
| LSMU0800858 | — | MR Conditional | Available |
| LSMU0800938 | — | MR Conditional | Available |
| LSMU0800958 | — | MR Conditional | Available |
| LSMU0801038 | — | MR Conditional | Available |
| LSMU0801058 | — | MR Conditional | Available |
| LSMU0801238 | — | MR Conditional | Available |
| LSMU0801258 | — | MR Conditional | Available |
| LSMU1350516 | — | MR Conditional | Available |
| LSMU1350526 | — | MR Conditional | Available |
| LSMU1350537 | — | MR Conditional | Available |
| LSMU1350616 | — | MR Conditional | Available |
| LSMU1350626 | — | MR Conditional | Available |
| LSMU1350637 | — | MR Conditional | Available |
| LSMU1350658 | — | MR Conditional | Available |
| LSMU1350716 | — | MR Conditional | Available |
| LSMU1350726 | — | MR Conditional | Available |
| LSMU1350737 | — | MR Conditional | Available |
| LSMU1350758 | — | MR Conditional | Available |
| LSMU1350816 | — | MR Conditional | Available |
| LSMU1350826 | — | MR Conditional | Available |
| LSMU1350837 | — | MR Conditional | Available |
| LSMU1350858 | — | MR Conditional | Available |
| LSMU1350938 | — | MR Conditional | Available |
| LSMU1350958 | — | MR Conditional | Available |
| LSMU1351038 | — | MR Conditional | Available |
| LSMU1351058 | — | MR Conditional | Available |
| LSMU1351238 | — | MR Conditional | Available |
| LSMU1351258 | — | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is LifeStream 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 LifeStream?
LifeStream is made by Clearstream Technologies Limited. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does LifeStream come in?
The FDA device database does not list sizes for LifeStream. Check the instructions for use or ask a Clearstream Technologies Limited representative.
Is LifeStream MRI safe?
The FDA device database lists LifeStream as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is LifeStream FDA cleared?
LifeStream is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Clearstream Technologies Limited sales representative?
Clearstream Technologies Limited has not listed representatives on LA Vascular yet. Visit the Clearstream Technologies Limited 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.