Terufusion Blood Administration Set - FDA Registration 744bd35eb34a939ebd9eff0f4fa8fff2

Access comprehensive regulatory information for Terufusion Blood Administration Set in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 744bd35eb34a939ebd9eff0f4fa8fff2 and manufactured by Terumo Corporation, Kofu factory. The device was registered on August 15, 2022.

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