Peripheral stents
Misago
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.
Misago 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 |
|---|---|---|---|
| SXR06040L | Length 40 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06060L | Length 60 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06080L | Length 80 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06100L | Length 100 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06120L | Length 120 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06150L | Length 150 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR07040L | Length 40 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR07060L | Length 60 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR07080L | Length 80 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR07100L | Length 100 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR07120L | Length 120 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR07150L | Length 150 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR08040L | Length 40 mm; Lumen/Inner Diameter 8 mm | MR Conditional | Available |
| SXR08060L | Length 60 mm; Lumen/Inner Diameter 8 mm | MR Conditional | Available |
| SXR08080L | Length 80 mm; Lumen/Inner Diameter 8 mm | MR Conditional | Available |
| SXR08100L | Length 100 mm; Lumen/Inner Diameter 8 mm | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is Misago 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 Misago?
Misago is made by Terumo Corporation. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does Misago come in?
Sizes listed for Misago: Length: 40–150 mm; Lumen/Inner Diameter: 6–8 mm. Confirm availability with the manufacturer's instructions for use.
Is Misago MRI safe?
The FDA device database lists Misago as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is Misago FDA cleared?
Misago is registered in the FDA's Global Unique Device Identification Database (GUDID).
How do I contact a Terumo Corporation sales representative?
Terumo Corporation has not listed representatives on LA Vascular yet. Visit the Terumo Corporation 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.