Australia TGA ARTG record

Nitrile examination/treatment glove, non-powdered

Australia TGA ARTG Registered Device · Pro-Tek Plastics Australia · Shijiazhuang Hongray Group Co Ltd · Class I · Started July 20, 2023

Good Name: Pro-Tek Plastics Australia - Nitrile examination/treatment glove, non-powdered

Device classification

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

Registration information

Start Date: July 20, 2023
Effective Date: July 20, 2023

Sponsor

Name: Pro-Tek Plastics Australia

Manufacturer

Name: Shijiazhuang Hongray Group Co Ltd
Country: China
Address: No 135 Xinhua West Road, Shiziazhuang City, Hebei Province, 0

Intended purpose

A non-sterile, single use glove intended to be worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes. It is used mainly as a two-way barrier to protect patients and staff

About this record

Access comprehensive regulatory information for Nitrile 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 Pro-Tek Plastics Australia, manufactured by Shijiazhuang Hongray Group Co Ltd in China. The device registration started on July 20, 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.