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Tourniquet, <specify> - ARTG 460886

Access comprehensive regulatory information for Tourniquet, <specify> in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is registered under ARTG number 460886 and sponsored by Brady Australia Pty Ltd, manufactured by Firstar Healthcare Company Ltd Guangzhou in China. The device registration started on August 27, 2024.

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 I
ARTG 460886
Class I
Tourniquet, <specify>
ARTG ID: 460886
Good Name: Brady Australia Pty Ltd - Tourniquet, <specify>
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Intended Purpose

Emergency tourniquet designed for rapid application to a limb in case of major haemorrhage

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
460886
Start Date
August 27, 2024
Effective Date
August 27, 2024
Manufacturer
Country
China
Address
Rm 901 Building No 2 Headquarters Center Tianan High tech Ecological Park, Panyu, Guangzhou, 511400