Electroencephalograph - FDA Registration 28e0ceddcb2af877700f7c8b7ab9e933

Access comprehensive regulatory information for Electroencephalograph in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 28e0ceddcb2af877700f7c8b7ab9e933 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on December 05, 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.