Peripheral stents
R2P 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.
R2P 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 |
|---|---|---|---|
| SXR06040R | Lumen/Inner Diameter 6 mm; Length 40 mm | MR Conditional | Available |
| SXR06060R | Length 60 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06080R | Length 80 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR06100R | Lumen/Inner Diameter 6 mm; Length 100 mm | MR Conditional | Available |
| SXR06120R | Lumen/Inner Diameter 6 mm; Length 120 mm | MR Conditional | Available |
| SXR06150R | Length 150 mm; Lumen/Inner Diameter 6 mm | MR Conditional | Available |
| SXR07040R | Lumen/Inner Diameter 7 mm; Length 40 mm | MR Conditional | Available |
| SXR07060R | Lumen/Inner Diameter 7 mm; Length 60 mm | MR Conditional | Available |
| SXR07080R | Lumen/Inner Diameter 7 mm; Length 80 mm | MR Conditional | Available |
| SXR07100R | Length 100 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR07120R | Lumen/Inner Diameter 7 mm; Length 120 mm | MR Conditional | Available |
| SXR07150R | Length 150 mm; Lumen/Inner Diameter 7 mm | MR Conditional | Available |
| SXR08040R | Lumen/Inner Diameter 8 mm; Length 40 mm | MR Conditional | Available |
| SXR08060R | Length 60 mm; Lumen/Inner Diameter 8 mm | MR Conditional | Available |
| SXR08080R | Length 80 mm; Lumen/Inner Diameter 8 mm | MR Conditional | Available |
| SXR08100R | Lumen/Inner Diameter 8 mm; Length 100 mm | MR Conditional | Available |
Procedures that use peripheral stents
Frequently asked questions
What is R2P 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 R2P Misago?
R2P Misago is made by Terumo Corporation. It is listed under peripheral artery stents and covered stents in our device library.
What sizes does R2P Misago come in?
Sizes listed for R2P Misago: Lumen/Inner Diameter: 6–8 mm; Length: 40–150 mm. Confirm availability with the manufacturer's instructions for use.
Is R2P Misago MRI safe?
The FDA device database lists R2P Misago as MR Conditional. Always follow the specific MRI conditions in the labeling.
Is R2P Misago FDA cleared?
R2P 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.