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Thrombectomy wire-net

Access comprehensive regulatory information for Thrombectomy wire-net in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by ACRA Regulatory Services Pty Ltd, manufactured by Inari Medical Inc in United States of America. The device registration started on December 22, 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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Class I
Class I
Thrombectomy wire-net
Australia TGA ARTG Registered Device
Good Name: ACRA Regulatory Services Pty Ltd - Thrombectomy wire-net
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Intended Purpose

The Thrombectomy System is indicated for: โ€ข The non-surgical removal of thrombi and emboli from blood vessels. โ€ข Injection, infusion, and/or aspiration of contrast media and other fluids into or from a blood vessel. The Thrombectomy System is intended for use in the peripheral vasculature including deep vein thrombosis (DVT).

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General-Export
Registration Information
Start Date
December 22, 2023
Effective Date
December 22, 2023
Manufacturer
Country
United States of America
Address
6001 Oak Canyon Suite 100 Irvine, CA, 92618