Duo Venous Stent System
Duo Hybrid and Duo Extend
Duo Venous Stent System
Duo Hybrid and Duo Extend
Engineered for greater crush resistance and flexibility, Duo Venous Stent System is built to address the multiple anatomical challenges of the deep venous system and includes two stents – Duo Hybrid and Duo Extend.¹ This distinctive portfolio of self-expending venous stents offers the ability to treat a broad range of patients with chronic venous insufficiency (CVI) – from simple to complex lesions. Duo Hybrid is designed to work independently or in conjunction with Duo Extend to provide clinical versatility.
Duo Venous Stent System includes two stents – Duo Hybrid and Duo Extend
Built to address the multiple anatomical challenges of the deep venous system
Engineered for greater crush resistance, flexibility and durability
Features
Duo Hybrid
Duo Hybrid features a distinct design that uniquely combines varied stent properties into a single stent without compromise. It seamlessly integrates precise mechanical properties along the stent length for targeted crush resistance, flexibility and durability.¹
Duo Extend
When additional coverage is needed, Duo Extend stent smoothly overlaps with Duo Hybrid to extend therapy. These two stents are designed to work together, minimizing the risk of stent fracture and corrosion, while providing an option to stent into caudal vein with a smaller diameter.¹
Note: Duo Extend is to be used only in combination with Duo Hybrid and is not indicated for independent use.
Triaxle delivery platform
The Duo Hybrid and Duo Extend stents are mounted on a familiar triaxial delivery platform. The combination of precise deployment, minimal foreshortening, and radiopaque markers that aid visualization under fluoroscopy, make delivery of the stents easy to plan and execute.¹
Specifications
- Duo Hybrid (14 mm stent diameter)
- Model number
- N1101410009120
- Stent length
- 100 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (14 mm stent diameter)
- Model number
- N1101412009120
- Stent length
- 120 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (14 mm stent diameter)
- Model number
- N1101414009120
- Stent length
- 140 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (14 mm stent diameter)
- Model number
- N1101416009120
- Stent length
- 160 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (16 mm stent diameter)
- Model number
- N1101610010120
- Stent length
- 100 mm
- Sheath compatibility
- 10 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (16 mm stent diameter)
- Model number
- N1101612010120
- Stent length
- 120 mm
- Sheath compatibility
- 10 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (16 mm stent diameter)
- Model number
- N1101614010120
- Stent length
- 140 mm
- Sheath compatibility
- 10 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (16 mm stent diameter)
- Model number
- N1101616010120
- Stent length
- 160 mm
- Sheath compatibility
- 10 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Hybrid (18 mm stent diameter)
- Model number
- N1101812010120
- Stent length
- 120 mm
- Sheath compatibility
- 10 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Extend (12 mm stent diameter)
- Model number
- N1201208009120
- Stent length
- 80 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Extend (12 mm stent diameter)
- Model number
- N1201212009120
- Stent length
- 120 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Extend (14 mm stent diameter)
- Model number
- N1201408009120
- Stent length
- 80 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Extend (14 mm stent diameter)
- Model number
- N1201412009120
- Stent length
- 120 mm
- Sheath compatibility
- 9 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
- Duo Extend (16 mm stent diameter)
- Model number
- N1201612010120
- Stent length
- 120 mm
- Sheath compatibility
- 10 F
- Maximum guidewire
- 0.035 inches
- Working length
- 120 cm
Recommended products
- Research has shown that IVC filters may have long-term complications and the FDA has published multiple safety communications recommending the removal of IVC filters when no longer indicated.¹,² Philips IVC Filter Removal Laser Sheath – CavaClear – is the first and only FDA-cleared solution for advanced IVC filter removal³ and was granted Breakthrough Device Designation (BDD). It is a state-of-the-art laser sheath designed to safely and predictably ablate scar tissue 360 degrees around an embedded IVC filter.⁴ CavaClear provides an effective, minimally invasive solution for embedded IVC filters, no matter the filter dwell time. CavaClear is backed by Philips support to train staff on device usage and mechanisms of action, as well as offer additional support to seamlessly integrate into your workflow.
- As an adjunct to conventional angiographic interventions, the Visions PV .035 digital IVUS catheter evaluates vascular morphology in blood vessels and provides cross-sectional imaging of these vessels. With a 90 cm length and 60 mm max imaging diameter for 0.035” guide wire interventional procedures, the device aids in peripheral artery disease diagnosis and venous disease and guides clinicians toward the correct therapy for the patient’s unique needs.
Disclaimer
1. Data on file: D062749
2. P230021 Summary of Safety and Effectiveness Document
Brief statement
Philips Duo Venous Stent System
Intended use:
The Duo Venous Stent System is intended for use in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction. The Duo Hybrid Stent is intended to be used in the iliac vein at the confluence of the inferior vena cava only. The Duo Extend Stent is intended for use in the common iliac and common femoral vein.
Contraindications for use:
The Duo Venous Stent System is contraindicated for the following: 1. Patients with a known hypersensitivity to nickel-titanium alloy (Nitinol). 2. Patients unable to receive standard medication used for interventional procedures including anticoagulants, contrast agents and antiplatelet therapy. 3. Patients who are judged to have a lesion that prevents complete inflation of a balloon dilation catheter or proper placement of the stent or the stent delivery system. 4. Tortuous vascular anatomy significant enough to prevent safe introduction and passage of the device to its intended location. 5. Duo Hybrid jugular or contralateral vascular access
Prior to implanting the Duo Venous Stent System, please review the instructions for use for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use.
Caution:
Federal law restricts this device to sale by or on the order of a physician.