Australia TGA ARTG recordEndotherapy forceps, biopsy, flexible, single-use
Australia TGA ARTG Registered Device · Steris Australia Pty Ltd · Hangzhou AGS MedTech Co Ltd · Class IIa · Started May 01, 2023
Good Name: Steris Australia Pty Ltd - Endotherapy forceps, biopsy, flexible, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- May 01, 2023
- Effective Date
- May 01, 2023
- Country
- China
- Address
- Building 5 Building 6 No 597 Kangxin Road Yuhang District Hangzhou Zhejiang, Peoples Republic of China, 311106
This device is used to enter human gastrointestinal tract via flexible endoscope to obtain tissue sample in order to understand disease pathology
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.