Light-Cured Dental Restorative Material (Beautifil II LS) (Giomer) - FDA Registration 0bd7f26ae430f7157871f4fd73cf7174

Access comprehensive regulatory information for Light-Cured Dental Restorative Material (Beautifil II LS) (Giomer) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0bd7f26ae430f7157871f4fd73cf7174 and manufactured by SHOFU INC.,JAPAN. The device was registered on January 08, 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.