Radiopaque Posterior Glass Ionomer Restorative Cement (A3.5) - FDA Registration 21a7e2d7848d9b7b36712a0d8a63ac3d

Access comprehensive regulatory information for Radiopaque Posterior Glass Ionomer Restorative Cement (A3.5) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 21a7e2d7848d9b7b36712a0d8a63ac3d and manufactured by GC Corporation Fuji Oyama Factory. The device was registered on November 17, 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.