Australia TGA ARTG recordHevea-latex examination/treatment glove, non-powdered
Australia TGA ARTG Registered Device · Australia Health Products Central Pty Ltd · CRDLight Optoelectronic Technology Co Ltd · Class I · Started March 31, 2022
Good Name: Australia Health Products Central Pty Ltd- Hevea-latex examination/treatment glove, non-powdered
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- March 31, 2022
- Effective Date
- March 31, 2022
- Country
- China
- Address
- Floor 1-5 Building No 7 & Floor 1-4 Building No 5 No 18 Xinyi Road, Jianghai District, Jiangmen City, Guangdong Province
This is a non-sterile device made of latex that is intended to be used s a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes to prevent cross contamination.
Access comprehensive regulatory information for Hevea-latex examination/treatment glove, non-powdered in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class I is sponsored by Australia Health Products Central Pty Ltd, manufactured by CRDLight Optoelectronic Technology Co Ltd in China. The device registration started on March 31, 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.