ELECTROENCEPHALOGRAPH SYSTEM-EEG-1250K & Accessories - FDA Registration 86f618eaa4d585f4c61ad8d88482e1a8

Access comprehensive regulatory information for ELECTROENCEPHALOGRAPH SYSTEM-EEG-1250K & Accessories in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 86f618eaa4d585f4c61ad8d88482e1a8 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on August 17, 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.