Australia flagARTG 212600

Hevea-latex examination/treatment glove, non-powdered

ARTG ID: 212600 · GIENIC PTY LTD · Top Glove Sdn Bhd · Class I · Started July 25, 2013

Good Name: GIENIC PTY LTD - Hevea-latex examination/treatment glove, non-powdered

Device classification
Risk Class
Class I
Product Type
Single Device Product
ARTG Category
General
Registration information
ARTG ID
212600
Start Date
July 25, 2013
Effective Date
July 25, 2013
Sponsor
Manufacturer
Country
Malaysia
Address
Lot 4969 Jalan Teratai Batu 6 off Jalan Meru, Klang, Selangor DE, 41050
Intended purpose

A non-sterile device made of Hevea natural rubber latex (NRL) intended as a protective barrier when worn on the hands of healthcare providers during patient examination/treatment or for other sanitary purposes; its inner surface is not covered with talcum powder. The device is used mainly as a two-way barrier to protect both the patient and the staff against various contamination. It will have appropriate characteristics regarding tactility and comfort of use, and should provide appropriate physical properties (e.g., tensile strength, resistance to puncture, elasticity), and uniformity of dimensions (i.e., sizing consistency). This is a single-use device

About this record

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 registered under ARTG number 212600 and sponsored by GIENIC PTY LTD, manufactured by Top Glove Sdn Bhd in Malaysia. The device registration started on July 25, 2013.

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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