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Endotherapy needle, single use - ARTG 470965

Access comprehensive regulatory information for Endotherapy needle, single use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 470965 and sponsored by Steris Australia Pty Ltd, manufactured by Zhejiang Chuangxiang Medical Technology Co Ltd in China. The device registration started on November 29, 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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Class IIa
ARTG 470965
Class IIa
Endotherapy needle, single use
ARTG ID: 470965
Good Name: Steris Australia Pty Ltd - Endotherapy needle, single use
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Intended Purpose

The device is used for endoscopic injection into gastrointestinal mucosa, or to endoscopically introduce a sclerosing agent into selected sites to control actual or potential bleeding lesions in the digestive system.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
470965
Start Date
November 29, 2024
Effective Date
November 29, 2024
Manufacturer
Country
China
Address
Room 101-1, 201-1, 301, 401 Building 50 No. 650 Hongfeng Road Donghu Street, Linping District, Hangzhou City, Zhejiang Province, 311100