DENU COMPOSITE RESIN - FDA Registration 3086dbd7588d6a40694b159a92db4df5

Access comprehensive regulatory information for DENU COMPOSITE RESIN in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 3086dbd7588d6a40694b159a92db4df5 and manufactured by HDI Inc. The device was registered on September 05, 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.