Terufusion Infusion Pump Type LF3 - FDA Registration 866b742f001de6e2dc63f5e3c24b81ae

Access comprehensive regulatory information for Terufusion Infusion Pump Type LF3 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 866b742f001de6e2dc63f5e3c24b81ae and manufactured by Ashitaka Factory of Terumo Corporation. The device was registered on April 20, 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.