Urea Kit ( Modified Berthelot Method) - FDA Registration 764ecdecad378f19ef75eca8442a4c22

Access comprehensive regulatory information for Urea Kit ( Modified Berthelot Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 764ecdecad378f19ef75eca8442a4c22 and manufactured by Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.. The device was registered on June 15, 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.