Light Cured Cavity Liner - FDA Registration 22b68de22416b0a2278d6ce4ad9414f8

Access comprehensive regulatory information for Light Cured Cavity Liner in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 22b68de22416b0a2278d6ce4ad9414f8 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.