Australia TGA ARTG recordHevea-latex examination/treatment glove, non-powdered
Australia TGA ARTG Registered Device · Aria Healthcare Pty Ltd · Wrp Asia Pacific Sdn Bhd · Class I · Started July 16, 2021
Good Name: Aria Healthcare Pty Ltd - Hevea-latex examination/treatment glove, non-powdered
- Risk Class
- Class I
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- July 16, 2021
- Effective Date
- July 16, 2021
- Country
- Malaysia
- Address
- Lot 1 Jalan 3 Kawasan Perusahaan Bandar Baru Salak Tinggi, Sepang, Selangor, 43900
Single-use Latex gloves intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes. The device is used mainly as a two-way barrier to protect both the patient and the staff against various 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 Aria Healthcare Pty Ltd, manufactured by Wrp Asia Pacific Sdn Bhd in Malaysia. The device registration started on July 16, 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.