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Infusion pump, analgesic, patient-controlled

Access comprehensive regulatory information for Infusion pump, analgesic, patient-controlled in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIb is sponsored by Fresenius Kabi Australia Pty Ltd, manufactured by Woo Young Medical Co Ltd in South Korea. The device registration started on December 08, 2010.

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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TGA ARTG Official Data
Class IIb
Class IIb
Infusion pump, analgesic, patient-controlled
Australia TGA ARTG Registered Device
Good Name: Fresenius Kabi Australia Pty Limited - Infusion pump, analgesic, patient-controlled
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Intended Purpose

A device that delivers a predetermined amount of intravenous or epidural narcotic analgesic when activated by the patient. It can be operated in a demand bolus or continuous mode.

Device Classification
Risk Class
Class IIb
Product Type
Single Device Product
ARTG Category
General
Registration Information
Start Date
December 08, 2010
Effective Date
December 08, 2010
Manufacturer
Country
South Korea
Address
374-3 Sangsin-Ri Jincheon-Eup, Jincheon-Gun, Chungcheongbuk-Do