Duo Venous Stent System
Duo Hybrid and Duo Extend
HCIGTDDVSSDHADEVenous stents
  • Product detail photograph
  • Product detail photograph
  • Main in use photograph
  • Product with accessory photograph
  • Front product photograph
  • Standard product photograph

Duo Venous Stent System

Duo Hybrid and Duo Extend
HCIGTDDVSSDHADEVenous stents
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.

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 Hybrid
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
Triaxle delivery platform
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.
Duo Extend


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


Documentation

Product brochure
PDF|5.74 MB

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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.