Australia TGA ARTG record

General-purpose syringe/needle

Australia TGA ARTG Registered Device · We Test Bio Pty Ltd · Jung Rim Medical Industrial Co Ltd · Class IIa · Started April 03, 2023

Good Name: We Test Bio Pty Ltd - General-purpose syringe/needle

Device classification

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

Registration information

Start Date: April 03, 2023
Effective Date: April 03, 2023

Sponsor

Name: We Test Bio Pty Ltd

Manufacturer

Name: Jung Rim Medical Industrial Co Ltd
Country: South Korea
Address: #187 Jingwang-ro lwol-myeon, Jincheon-gun, Chungcheongbuk-do

Intended purpose

A sterile device consisting of a transparent barrel with plunger (including a needle) intended to be used for injection/withdrawal of fluids to/from a medical device or the body. It is intended for various medical applications, including medication administration. This is a single-use device.

About this record

Access comprehensive regulatory information for General-purpose syringe/needle in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by We Test Bio Pty Ltd, manufactured by Jung Rim Medical Industrial Co Ltd in South Korea. The device registration started on April 03, 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.