NITINOL HYDROPHILIC GUIDEWIRE - MDA Registration GB2681124-161762

Access comprehensive regulatory information for NITINOL HYDROPHILIC GUIDEWIRE in the Malaysia medical device market through Pure Global AI's free database. This B medical device is registered under MDA ID GB2681124-161762 with brand name SUPREMO. The device was registered on February 05, 2024.

This page provides complete registration details including authorized representative details, brand information, and regulatory compliance data from the official Malaysia MDA medical device database. Pure Global AI offers free access to Malaysia's complete medical device registry.