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Important Notice
This Inari Medical website and all product offerings listed are tailored for the United States only. Please be aware that product availability and regulatory claims may vary in other regions we serve, including Europe, the Middle East, and Africa (EMEA), Asia-Pacific (APAC), and Latin America/Canada. Inari Medical is currently developing separate websites for our products tailored to these other global and regional markets.
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The Next Generation in Flow Restoration
InThrill™
Thrombectomy
System
Built upon a familiar platform optimized for efficient clot removal,
InThrill is the new standard for fast, full luminal clot removal in small vessels and AV accesses.
Redesigned with feedback from physicians and performance in mind, the next generation InThrill Thrombectomy System aims to efficiently remove full luminal clot from AV accesss and small vessels in half the passes compared to the first generation system.*
The InThrill Thrombectomy System
KEY FEATURES
  • Newly redesigned nitinol element for wall-to-wall clot removal in 4-10 mm vessels
  • Efficient 8 Fr system designed for fast clot removal in as few as two passes*
  • Ergonomic backend for a streamlined user experience and procedure workflow
SYSTEM TOOLKIT
Engineered to maximize the removal
of acute to chronic thrombus
InThrill Thrombectomy Catheter
InThrill Sheath
*Benchtop testing data on file
Indications for Use:
The InThrill Thrombectomy System is indicated for (1) the non-surgical removal of thrombi and emboli from blood vessels, including arteriovenous fistulae and arteriovenous grafts for dialysis access, and synthetic grafts and (2) injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel/graft. The InThrill thrombectomy system is intended for use in the peripheral vasculature. The InThrill thrombectomy system is not intended for use in deep vein thrombosis (DVT) treatment. The InThrill Sheath is indicated for use as a conduit for the insertion of endovascular devices into the peripheral vasculature while minimizing blood loss associated with such insertions.

Refer to IFU for complete Indications for Use, contraindications, warnings, and precautions.

Caution:
Federal (USA) law restricts this device to sale by or on the order of a physician.

All trademarks are property of their respective owners.

PRO-2365-USA-EN-v1