Australia flagARTG 474249

Nitrile examination/treatment glove, non-powdered

ARTG ID: 474249 · Pro-Tek Plastics Australia · Pro-Tek Plastics Australia · Class I · Started December 20, 2024

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
ARTG ID
474249
Start Date
December 20, 2024
Effective Date
December 20, 2024
Sponsor
Manufacturer
Country
Australia
Address
39 Scanlon Drive, Epping, VIC, 3076
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 registered under ARTG number 474249 and sponsored by Pro-Tek Plastics Australia, manufactured by Pro-Tek Plastics Australia in Australia. The device registration started on December 20, 2024.

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.

Free DatabasePowered by Pure Global AITGA ARTG Official Data