Australia TGA ARTG recordEndotherapy forceps, biopsy, flexible, single-use
Australia TGA ARTG Registered Device · Vitramed Pty Ltd · Hangzhou AGS MedTech Co Ltd · Class IIa · Started September 06, 2022
Good Name: Vitramed Pty Ltd - Endotherapy forceps, biopsy, flexible, single-use
- Risk Class
- Class IIa
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- September 06, 2022
- Effective Date
- September 06, 2022
- Name
- Vitramed Pty Ltd
- 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 the human gastrointestinal tract (stomach or duodenum) via flexible endoscope to obtain tissue sample for histological examination. This device is single use only.
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 Vitramed Pty Ltd, manufactured by Hangzhou AGS MedTech Co Ltd in China. The device registration started on September 06, 2022.
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.