Boston Scientific Watchman FLX (Left Atrial Appendage Closure Device)

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Specifications

  1. Device Sizes:
    • Available in multiple sizes ranging from 20 mm to 35 mm, ensuring precise fit across various anatomies.
  2. Material:
    • Constructed of a nitinol frame with a polyethylene terephthalate (PET) membrane covering the atrial-facing surface.
  3. Design Features:
    • Fully rounded frame for minimal trauma during implantation.
    • 45-degree struts designed to accommodate a wider range of LAA anatomies.
    • Stabilization anchors for secure placement and reduced migration risk.
  4. Delivery System:
    • Flexible delivery catheter with a distal articulation mechanism for controlled deployment.
    • Enhanced maneuverability for accurate placement.
  5. Imaging Requirements:
    • Compatible with transesophageal echocardiography (TEE) and fluoroscopy for procedural guidance.
  6. Anticoagulation Protocol:
    • Requires short-term anticoagulation therapy post-implantation (typically 45 days), transitioning to aspirin-only or dual antiplatelet therapy based on patient evaluation.

Description

Boston Scientific Watchman FLX (Left Atrial Appendage Closure Device)

    • Flexibility for Complex Anatomies:
      • The Watchman FLX can adapt to various LAA shapes and sizes, making it suitable for a broader range of patients compared to previous models.
    • Enhanced Safety:
      • The fully rounded design minimizes tissue injury and complications during implantation.
    • Complete LAA Sealing:
      • The PET membrane ensures complete occlusion, reducing the risk of blood clots escaping the LAA.
    • Improved Implantation Success Rates:
      • Simplified delivery and deployment systems contribute to higher procedural success.
    • Long-Term Solution:
      • Offers a permanent alternative to long-term oral anticoagulants, which can pose bleeding risks.
    • The Watchman FLX is an advanced Left Atrial Appendage Closure (LAAC) device designed to reduce stroke risk in patients with non-valvular atrial fibrillation (NVAF) who are unsuitable for long-term anticoagulation therapy. This innovative device permanently seals the left atrial appendage (LAA), a common site for blood clot formation in NVAF patients.

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