Australia TGA ARTG record

Electric infusion pump administration set

Australia TGA ARTG Registered Device · Baxter Healthcare Pty Ltd · Micrel Medical Devices SA · Class IIa · Started December 11, 2015

Good Name: Baxter Healthcare Pty Ltd - Electric infusion pump administration set

Device classification

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

Registration information

Start Date: December 11, 2015
Effective Date: December 11, 2015

Sponsor

Name: Baxter Healthcare Pty Ltd

Manufacturer

Name: Micrel Medical Devices SA
Country: Greece
Address: 42 Konstantinoupoleos str Koropi, Athens, Greece, 19441

Intended purpose

A collection of sterile devices (e.g., plastic tubing, check valve, roller clamp, Y-site connector, Luer, needle/catheter) intended to be used in combination with an electrically-powered infusion pump for the intravenous (IV), subcutaneous, intramuscular, or epidural administration. This is a single-use device.

About this record

Access comprehensive regulatory information for Electric infusion pump administration set in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is sponsored by Baxter Healthcare Pty Ltd, manufactured by Micrel Medical Devices SA in Greece. The device registration started on December 11, 2015.

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.