Demonstrated shorter procedural times when compared against Wallstent, Precise Pro, CGUARD and Xact1
The ROADSAVER Stent System takes performance to the next level.
The ROADSAVER Carotid Stent System is indicated for use with the NANOPARASOLTM Embolic Protection System.
The NANOPARASOL system is an embolic protection device designed to capture and remove dislodged debris during a carotid artery interventional procedure.1
The ROADSAVER Carotid Stent System offers technical improvements relative to single-layer carotid stents, including inner micromesh layer ensuring sustained embolic protection during and after CAS and flexible low-crossing profile delivery system, good in-vessel flexibility and good wall apposition in tortious Anatomies.1-4.
Clinical performance of the ROADSAVER stent system demonstrated a high procedure success rate, operator specialty independence and is supported by evidence confirming that these technical advancements translate into favorable safety and efficacy profile of the device.1-4
The ROADSAVER Stent System is supported by three key registration studies, one of which is the largest real-world study performed on a single-layer dual layer micro mesh stent.
Conclusion: The event rate for ipsilateral stroke up to 1 year post-procedure was 2.7%.
Conclusion: The rate of MAE in patients with normal CEA risk was 1.2%5
Conclusion: Low 30-day MAE rate and TLR rates of 2.2% and 0.8% respectively.6
Incidence of New Ischaemic Brain Lesions After Carotid Artery Stenting with the Micromesh Roadsaver Carotid Artery Stent: A Prospective Single-Centre Study7
· Single Center, 23 consecutive Carotid Artery Stenting procedures performed with the Roadsaver Stent
· Distal Protection devices used in all cases
· All lesions identified were asymptomatic with median volume of 0.076 cm3
· All lesions identified at discharge resolved at upon 30 day Diffusion Weighted MRI imaging
· No new Ischemic lesions identified on 30 day DW-MRI Follow up
Conclusion: The study showed protected effect of micromesh ROADSAVER stent during and post CAS procedure.7
Conclusion: No significant differences in baseline characteristics were found among the four groups.8
Conclusion: The study showed that the use of TCAR and ROADSAVER could be a safe alternative to CAE even in symptomatic and elderly patients.9
More Patients. More Options.
As expanded coverage of carotid artery stents shifts, the ROADSAVER Stent System offers the configuration options for treating more patients.
Expanded CMS guidelines2 now include coverage of:
• Patients with symptomatic carotid artery stenosis ≥50%
• Patients with asymptomatic carotid artery stenosis ≥70%
Email: Reimbursement@terumomedical.com
Contact: 855-380-3081
| Product Code | Product Description | Unconstrained Dimensions (mm) | Implanted Dimensions (mm) | |||||||
| Vessel Ø 1 mm Smaller than Unconstrained Ø | Vessel Ø 2 mm Smaller than Unconstrained Ø | |||||||||
| Diameter | Overall Length | Dual Layer Length | Vessel Diameter | Dual Layer Length | Overall Length | Vessel Diameter | Dual Layer Length | Overall Length | ||
| RDS-0520-143RX | 5mm x 20mm x 143cm | 5 | 25 | 20 | 4 | 20 | 33 | 3.5* | 25 | 34 |
| RDS-0530-143RX | 5mm x 30mm x 143cm | 5 | 37 | 30 | 4 | 35 | 47 | 3.5* | 40 | 50 |
| RDS-0540-143RX | 5mm x 40mm x 143cm | 5 | 47 | 40 | 4 | 45 | 59 | 3.5* | 52 | 62 |
| RDS-0616-143RX | 6mm x 16mm x 143cm | 6 | 22 | 16 | 5 | 20 | 32 | 4 | 23 | 35 |
| RDS-0625-143RX | 6mm x 25mm x 143cm | 6 | 33 | 25 | 5 | 30 | 44 | 4 | 33 | 48 |
| RDS-0630-143RX | 6mm x 30mm x 143cm | 6 | 40 | 30 | 5 | 40 | 53 | 4 | 43 | 58 |
| RDS-0718-143RX | 7mm x 18mm x 143cm | 7 | 25 | 18 | 6 | 23 | 35 | 5 | 26 | 38 |
| RDS-0725-143RX | 7mm x 25mm x 143cm | 7 | 35 | 25 | 6 | 30 | 47 | 5 | 36 | 52 |
| RDS-0730-143RX | 7mm x 30mm x 143cm | 7 | 40 | 30 | 6 | 40 | 53 | 5 | 44 | 60 |
| RDS-0820-143RX | 8mm x 20mm x 143cm | 8 | 25 | 20 | 7 | 25 | 36 | 6 | 27 | 40 |
| RDS-0825-143RX | 8mm x 25mm x 143cm | 8 | 35 | 25 | 7 | 30 | 49 | 6 | 38 | 54 |
| RDS-0830-143RX | 8mm x 30mm x 143cm | 8 | 40 | 30 | 7 | 40 | 55 | 6 | 45 | 61 |
| RDS-0840-143RX | 8mm x 40mm x 143cm | 8 | 47 | 40 | 7 | 50 | 67 | 6 | 60 | 75 |
| RDS-0920-143RX | 9mm x 20mm x 143cm | 9 | 33 | 20 | 8 | 30 | 45 | 7 | 33 | 48 |
| RDS-0930-143RX | 9mm x 30mm x 143cm | 9 | 40 | 30 | 8 | 40 | 55 | 7 | 45 | 60 |
| RDS-1020-143RX | 10mm x 20mm x 143cm | 10 | 35 | 20 | 9 | 30 | 45 | 8 | 35 | 50 |
| RDS-1030-143RX | 10mm x 30mm x 143cm | 10 | 43 | 30 | 9 | 40 | 55 | 8 | 45 | 60 |
| Model Number | Labeled Filter Size | Unconstrained Filter OD (mm) | Reference Vessel Diameters (mm) | |||||||
| PNP4514C-190 | SMALL | 5.2 | 3.0 – 4.5 | |||||||
| PNP6514C-190 | LARGE | 7.2 | 4.5 – 6.5 | |||||||
Carotid stent MRI safety: Is the ROADSAVER carotid stent system MRI-safe?
The ROADSAVER Carotid Stent System is MRI Conditional. This means that a patient implanted with the device may undergo MRI scans only under specific conditions. Scanning outside of these conditions may result in serious patient injury. Patients are instructed to refer to their patient implant card for additional information.
For complete MRI safety information, please consult the MRI Safety information section of the ROADSAVER Stent System Instructions for Use (IFU).
*Data derived from the referenced OUS study and may not be representative of Confidence clinical study performance.
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ROADSAVER Carotid Stent System
INDICATIONS FOR USE
The ROADSAVER Carotid Stent System, when used in conjunction with the Nanoparasol Embolic Protection System (EPS), is indicated for the treatment of carotid artery stenosis in patients with elevated risk for adverse events following carotid endarterectomy and meet the criteria outlined below:
AND
2. Patients having a vessel with reference diameters between 3.5 mm and 9.0 mm at the target lesion.
CONTRAINDICATIONS
The ROADSAVER Carotid Stent System is contraindicated for use in:
NANOPARASOL Embolic Protection System
INDICATIONS FOR USE
The NANOPARASOL EPS is indicated for use as a guidewire to contain and remove embolic material (thrombus/debris) while performing angioplasty and stenting procedures in carotid arteries. The diameter of the artery at the site of the filter placement should be between 3.0 and 6.5 mm.
CONTRAINDICATIONS
The NANOPARASOL Embolic Protection System is contraindicated for use in: