Central Monitor - FDA Registration 6a9fbe6969c1150f7f1238b89ce26c14

Access comprehensive regulatory information for Central Monitor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6a9fbe6969c1150f7f1238b89ce26c14 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on June 21, 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.