SELUTION SLR PTA Drug Eluting BalloonProduct Code (REF): SE18-020100
SELUTION SLR™ is a Sirolimus Drug-Eluting Balloon developed to provide consistent and predictable Limus drug release for up to 90 days. Its proprietary CELL ADHERENT TECHNOLOGY™ combines a phospholipid carrier with MicroReservoirs to support drug uptake and sustained retention in the treated tissue. This page documents the PTA configuration of SELUTION SLR: an over-the-wire (OTW) catheter with 0.018 inch guidewire compatibility, 135 cm usable length and balloon diameters from 2.00 mm to 7.00 mm, as published by Cordis for peripheral artery interventions. The proprietary phospholipid coating facilitates drug uptake and retention in the tissue, with minimal drug loss during the procedure while supporting excellent deliverability. MicroReservoirs are designed to achieve consistent and predictable drug release at a therapeutic level, comparable to modern drug-eluting stent technology. The broad size matrix — six balloon lengths from 40 mm to 150 mm across eight diameters — is designed to extend treatment options for peripheral artery disease, depending on the selected product configuration and approved indication. Product information on this page is presented as manufacturer-provided technical information; refer to the official Cordis instructions for use for indications, contraindications, warnings and precautions.
This page documents catalog code (REF) SE18-020100, one of 48 available configurations of the SELUTION SLR PTA Drug Eluting Balloon. See the full SELUTION SLR PTA Drug Eluting Balloon overview for every configuration.
Available under product codes SE18-020040, SE18-020060, SE18-020080, SE18-020100, SE18-020120, SE18-020150, SE18-025040, SE18-025060 and 40 more (see Ordering Information below).
Sizes & Specifications
- Sirolimus drug dose
- 1.0 µg/mm²
- Drug carrier
- CELL ADHERENT TECHNOLOGY™ — amphipathic lipid carrier
- Catheter design
- Over-the-Wire (OTW)
- Catheter usable length
- 135 cm
- Guidewire compatibility
- 0.018″
- Tip entry profile
- 0.021″
- Nominal balloon pressure
- 6 bar
- Rated burst pressure
- 12 bar for 40 mm balloon lengths; 10 bar for 60 – 150 mm balloon lengths
- Balloon diameters
- 2.00 – 7.00 mm (8 diameters)
- Balloon lengths
- 40, 60, 80, 100, 120, 150 mm
- Introducer sheath compatibility
- ≥ 5 Fr for 2.00 – 3.00 mm; ≥ 6 Fr for 3.50 – 5.00 mm; ≥ 7 Fr for 6.00 – 7.00 mm balloon diameters
Manufacturer: Cordis · Reference source: cordis.com
Product Features
Design characteristics as published by Cordis.
Proprietary Phospholipid Coating
Facilitates drug uptake and retention in the tissue, with minimal drug loss during the procedure while supporting excellent deliverability.
MicroReservoirs
Designed to achieve consistent and predictable drug release at a therapeutic level, comparable to modern drug-eluting stent technology.
Broad Size Matrix
A broad size portfolio designed to extend treatment options for peripheral artery disease, depending on the selected product configuration and approved indication.
Sustained Limus Release
Developed to provide consistent and predictable Limus drug release for up to 90 days.
Documentation
Official IFU, sizing charts and full specifications are available on request through Azmed Devices.
Product Identification & Specifications
Reference identifiers for procurement, registration and tender documentation.
| Product Code | SE18-020100 |
|---|---|
| REF Numbers | SE18-020040, SE18-020060, SE18-020080, SE18-020100, SE18-020120, SE18-020150, SE18-025040, SE18-025060, SE18-025080, SE18-025100, SE18-025120, SE18-025150, SE18-030040, SE18-030060, SE18-030080, SE18-030100, SE18-030120, SE18-030150, SE18-035040, SE18-035060, SE18-035080, SE18-035100, SE18-035120, SE18-035150, SE18-040040, SE18-040060, SE18-040080, SE18-040100, SE18-040120, SE18-040150, SE18-050040, SE18-050060, SE18-050080, SE18-050100, SE18-050120, SE18-050150, SE18-060040, SE18-060060, SE18-060080, SE18-060100, SE18-060120, SE18-060150, SE18-070040, SE18-070060, SE18-070080, SE18-070100, SE18-070120, SE18-070150 |
| Manufacturer | Cordis |
| Brand | Cordis |
| Product Family | Peripheral & Endovascular |
| Country Availability | Azerbaijan |
Clinical Applications
The SELUTION SLR PTA Drug Eluting Balloon is a pta peripheral sirolimus drug eluting balloon in the Peripheral & Endovascular family from Cordis, used by interventional specialists in procedures where a pta peripheral sirolimus drug eluting balloon of this class is indicated. It is supplied in 48 configurations (catalog codes SE18-020040 through SE18-070150) to match anatomical and procedural requirements.
For the complete indications for use, contraindications and instructions for use (IFU), request the official Cordis documentation through our clinical team. Azmed Devices supplies the SELUTION SLR PTA Drug Eluting Balloon to hospitals and clinics across Azerbaijan.
Ordering Information
Catalog reference codes as published by Cordis. Contact us to confirm current availability.
Showing 48 of 48 configurations
| Balloon diameter (mm) | Balloon length (mm) | REF |
|---|---|---|
| 2.00 | 40 | SE18-020040 |
| 2.00 | 60 | SE18-020060 |
| 2.00 | 80 | SE18-020080 |
| 2.00 | 100 | SE18-020100 |
| 2.00 | 120 | SE18-020120 |
| 2.00 | 150 | SE18-020150 |
| 2.50 | 40 | SE18-025040 |
| 2.50 | 60 | SE18-025060 |
| 2.50 | 80 | SE18-025080 |
| 2.50 | 100 | SE18-025100 |
| 2.50 | 120 | SE18-025120 |
| 2.50 | 150 | SE18-025150 |
| 3.00 | 40 | SE18-030040 |
| 3.00 | 60 | SE18-030060 |
| 3.00 | 80 | SE18-030080 |
| 3.00 | 100 | SE18-030100 |
| 3.00 | 120 | SE18-030120 |
| 3.00 | 150 | SE18-030150 |
| 3.50 | 40 | SE18-035040 |
| 3.50 | 60 | SE18-035060 |
| 3.50 | 80 | SE18-035080 |
| 3.50 | 100 | SE18-035100 |
| 3.50 | 120 | SE18-035120 |
| 3.50 | 150 | SE18-035150 |
| 4.00 | 40 | SE18-040040 |
| 4.00 | 60 | SE18-040060 |
| 4.00 | 80 | SE18-040080 |
| 4.00 | 100 | SE18-040100 |
| 4.00 | 120 | SE18-040120 |
| 4.00 | 150 | SE18-040150 |
| 5.00 | 40 | SE18-050040 |
| 5.00 | 60 | SE18-050060 |
| 5.00 | 80 | SE18-050080 |
| 5.00 | 100 | SE18-050100 |
| 5.00 | 120 | SE18-050120 |
| 5.00 | 150 | SE18-050150 |
| 6.00 | 40 | SE18-060040 |
| 6.00 | 60 | SE18-060060 |
| 6.00 | 80 | SE18-060080 |
| 6.00 | 100 | SE18-060100 |
| 6.00 | 120 | SE18-060120 |
| 6.00 | 150 | SE18-060150 |
| 7.00 | 40 | SE18-070040 |
| 7.00 | 60 | SE18-070060 |
| 7.00 | 80 | SE18-070080 |
| 7.00 | 100 | SE18-070100 |
| 7.00 | 120 | SE18-070120 |
| 7.00 | 150 | SE18-070150 |
Size matrix and REF codes from the official Cordis SELUTION SLR ordering information (100644297, 06/2024). Introducer sheath compatibility: ≥ 5 Fr for 2.00 – 3.00 mm, ≥ 6 Fr for 3.50 – 5.00 mm, ≥ 7 Fr for 6.00 – 7.00 mm balloon diameters.
Downloads & Documentation
Instructions for use (IFU), technical datasheets and clinical literature for the SELUTION SLR PTA Drug Eluting Balloon are available on request from our clinical team.
Request DocumentationFrequently Asked Questions
- Is this the coronary or peripheral version of SELUTION SLR?
- This page documents the PTA (peripheral) configuration with 0.018″ guidewire compatibility and balloon diameters from 2.00 mm to 7.00 mm. The coronary PTCA configuration is documented on a separate product page and uses different sizes and REF codes.
- How long does SELUTION SLR provide drug release?
- It is developed to provide consistent and predictable Limus drug release for up to 90 days.
- What guidewire is the SELUTION SLR PTA balloon compatible with?
- The PTA configuration is an over-the-wire (OTW) catheter compatible with 0.018″ guidewires, with a 135 cm usable catheter length.
- How can our hospital order SELUTION SLR PTA Drug Eluting Balloon in Azerbaijan?
- Contact Azmed Devices at info@azmeddevices.com. We provide manufacturer documentation, registration status and tender support, and coordinate supply directly with Cordis.
