Australia TGA ARTG record

Vitreous body prosthesis

Australia TGA ARTG Registered Device · Emagin Pty Ltd · Guangzhou Vesber Biotechnology Co Ltd · Class IIb · Started November 04, 2021

Good Name: Emagin Pty Ltd - Vitreous body prosthesis

Device classification

Risk Class: Class IIb
Product Type: Single Device Product
ARTG Category: General

Registration information

Start Date: November 04, 2021
Effective Date: November 04, 2021

Sponsor

Name: Emagin Pty Ltd

Manufacturer

Name: Guangzhou Vesber Biotechnology Co Ltd
Country: China
Address: B501 No 1 Kesheng Road Guangzhou Private Science Park 1633 Beitai Road, Baiyun District, Guangzhou, 510540

Intended purpose

Foldable Capsular Vitreous Body made from a biocompatible polymer and contains a vitreous-like capsule, drain tube and drain valve. The silicone oil could be injected into the capsule via a drain valve to support the retina and eyeball.

About this record

Access comprehensive regulatory information for Vitreous body prosthesis in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Emagin Pty Ltd, manufactured by Guangzhou Vesber Biotechnology Co Ltd in China. The device registration started on November 04, 2021.

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.