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Thrombuster Pro GR - Embolectomy/thrombectomy suction catheter - ARTG 482408

Access comprehensive regulatory information for Thrombuster Pro GR - Embolectomy/thrombectomy suction catheter in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 482408 and sponsored by Bio-Excel Australia Pty Ltd, manufactured by Kaneka Corporation in Japan. The device registration started on March 13, 2025.

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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TGA ARTG Official Data
Class III
ARTG 482408
Class III
Thrombuster Pro GR - Embolectomy/thrombectomy suction catheter
ARTG ID: 482408
Good Name: Bio-Excel Australia Pty Ltd - Thrombuster Pro GR - Embolectomy/thrombectomy suction catheter
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Intended Purpose

This product is used for the purpose of percutaneously removing thrombi from peripheral blood vessels, and suctioning and removing thrombi from the coronary artery.

Device Classification
Risk Class
Class III
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
482408
Start Date
March 13, 2025
Effective Date
March 13, 2025
Manufacturer
Country
Japan
Address
3-18 2-Chome Nakanoshima, Kita Ku, Osaka, 530-8288