Suture, polypropylene monofilament - ARTG 414859
Access comprehensive regulatory information for Suture, polypropylene monofilament in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 414859 and sponsored by Pacific Dental Specialties Pty Ltd, manufactured by Osteogenics Biomedical Inc in United States of America. The device registration started on July 28, 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.
Cytoplast PTFE Suture is indicated for use in most types of soft tissue approximation and/or ligation, including dental surgeries. Cytoplast PTFE Suture is designed for short term use and must be removed. The device is not indicated for use in cardiovascular surgery, ophthalmic surgery, microsurgery and central/peripheral neural tissue surgery.