Manual blood lancing device, single-use - ARTG 467885

Access comprehensive regulatory information for Manual blood lancing device, single-use in the Australia medical device market through Pure Global AI's free TGA ARTG database. This Class IIa is registered under ARTG number 467885 and sponsored by Genesis Biotech Pty Ltd, manufactured by Shandong Lianfa Medical Plastic Products Co Ltd in China. The device registration started on November 10, 2024.

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.