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Nitrile examination/treatment glove, non-powdered - ARTG 413839

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 registered under ARTG number 413839 and 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.

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TGA ARTG Official Data
Class I
ARTG 413839
Class I
Nitrile examination/treatment glove, non-powdered
ARTG ID: 413839
Good Name: Pro-Tek Plastics Australia - Nitrile examination/treatment glove, non-powdered
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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

Device Classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
413839
Start Date
July 20, 2023
Effective Date
July 20, 2023
Manufacturer
Country
China
Address
No 135 Xinhua West Road, Shiziazhuang City, Hebei Province, 0