GlasIonomer FX Ultra - FDA Registration ea54d0ad05d40c7b72e7fbe62c930aa6

Access comprehensive regulatory information for GlasIonomer FX Ultra in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ea54d0ad05d40c7b72e7fbe62c930aa6 and manufactured by SHOFU INC.,JAPAN. The device was registered on April 28, 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.