Patient Monitor - FDA Registration 93821c97069d78cbab56fc210bca0fee

Access comprehensive regulatory information for Patient Monitor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 93821c97069d78cbab56fc210bca0fee and manufactured by Bistos Co., Ltd. The device was registered on April 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.