Sleep Diagnostic System - FDA Registration 0524becf7db6d00a04a233d84542e11b

Access comprehensive regulatory information for Sleep Diagnostic System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0524becf7db6d00a04a233d84542e11b and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on July 14, 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.