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InThrill Thrombectomy System - Thrombectomy wire-net

Australia TGA ARTG Registered Device · ACRA Regulatory Services Pty Ltd · Inari Medical Inc · Class IIa · Started May 15, 2023

Good Name: ACRA Regulatory Services Pty Ltd - InThrill Thrombectomy System - Thrombectomy wire-net

Device classification
Risk Class
Class IIa
Product Type
Medical device system
ARTG Category
General
Registration information
Start Date
May 15, 2023
Effective Date
May 15, 2023
Sponsor
Manufacturer
Country
United States of America
Address
6001 Oak Canyon Suite 100 Irvine, CA, 92618
Intended purpose

Sterile Thrombectomy System is indicated for: - The non-surgical removal of thrombi and emboli from blood vessels, including arteriovenous fistulae and arteriovenous grafts for dialysis access, and synthetic grafts. - Injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel/graft. The Thrombectomy System is intended for use in the peripheral vasculature. The Thrombectomy System is not intended for use in deep vein thrombosis (DVT) treatment.

About this record

Access comprehensive regulatory information for InThrill Thrombectomy System - Thrombectomy wire-net in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by ACRA Regulatory Services Pty Ltd, manufactured by Inari Medical Inc in United States of America. The device registration started on May 15, 2023.

This page provides complete registration details including sponsor information, manufacturer details, and regulatory compliance data from the official Australia TGA ARTG medical device database. Pure Global AI offers free access to Australia's complete medical device registry with 131,000+ devices, helping global MedTech companies navigate TGA regulations efficiently.

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