DENU FLOW RESIN - FDA Registration d85863455f505ba4052cac1842d1293e

Access comprehensive regulatory information for DENU FLOW RESIN in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d85863455f505ba4052cac1842d1293e and manufactured by HDI Inc. 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.