Bedside Monitor - FDA Registration 5d9be4d7c225943f2a6e8d203331f997

Access comprehensive regulatory information for Bedside Monitor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 5d9be4d7c225943f2a6e8d203331f997 and manufactured by Nihon Kohden Tomioka Corporation Tomioka Production Center. The device was registered on November 28, 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.