Australia TGA ARTG recordInfusion pump, analgesic, patient-controlled
Australia TGA ARTG Registered Device · Fresenius Kabi Australia Pty Ltd · Woo Young Medical Co Ltd · Class IIb · Started December 08, 2010
Good Name: Fresenius Kabi Australia Pty Limited - Infusion pump, analgesic, patient-controlled
- Risk Class
- Class IIb
- Product Type
- Single Device Product
- ARTG Category
- General
- Start Date
- December 08, 2010
- Effective Date
- December 08, 2010
- Country
- South Korea
- Address
- 374-3 Sangsin-Ri Jincheon-Eup, Jincheon-Gun, Chungcheongbuk-Do
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.
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.