Hemopatch Sealing Hemostat - Collagen haemostatic agent - ARTG 477685
Access comprehensive regulatory information for Hemopatch Sealing Hemostat - Collagen haemostatic agent in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class III is registered under ARTG number 477685 and sponsored by Baxter Healthcare Pty Ltd, manufactured by Baxter Healthcare SA in Switzerland. The device registration started on February 04, 2025.
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.
HEMOPATCH is indicated as a haemostatic device and surgical sealant for procedures in which control of bleeding or leakage of other body fluids by conventional surgical techniques is either ineffective or impractical.