Urea (UREA) Kit (Urease-GLDH Method) - FDA Registration e5016080fd91861852cb81daaf32e339

Access comprehensive regulatory information for Urea (UREA) Kit (Urease-GLDH Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID e5016080fd91861852cb81daaf32e339 and manufactured by Zybio Inc.. The device was registered on December 16, 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.