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Endotherapy forceps, biopsy, flexible, single-use

Access comprehensive regulatory information for Endotherapy forceps, biopsy, flexible, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Steris Australia Pty Ltd, manufactured by Hangzhou AGS MedTech Co Ltd in China. The device registration started on May 01, 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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TGA ARTG Official Data
Class IIa
Class IIa
Endotherapy forceps, biopsy, flexible, single-use
Australia TGA ARTG Registered Device
Good Name: Steris Australia Pty Ltd - Endotherapy forceps, biopsy, flexible, single-use
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Intended Purpose

This device is used to enter human gastrointestinal tract via flexible endoscope to obtain tissue sample in order to understand disease pathology

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
May 01, 2023
Effective Date
May 01, 2023
Manufacturer
Country
China
Address
Building 5 Building 6 No 597 Kangxin Road Yuhang District Hangzhou Zhejiang, Peoples Republic of China, 311106