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Electric infusion pump administration set - ARTG 265815

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 registered under ARTG number 265815 and 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.

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Class IIa
ARTG 265815
Class IIa
Electric infusion pump administration set
ARTG ID: 265815
Good Name: Baxter Healthcare Pty Ltd - Electric infusion pump administration set
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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.

Device Classification
Risk Class
Class IIa
Product Type
Single Device Product
ARTG Category
General
Registration Information
ARTG ID
265815
Start Date
December 11, 2015
Effective Date
December 11, 2015
Manufacturer
Country
Greece
Address
42 Konstantinoupoleos str Koropi, Athens, Greece, 19441