PROVIDO - FDA Registration 725017565b6a779095fcd6978e3c64c3

Access comprehensive regulatory information for PROVIDO in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 725017565b6a779095fcd6978e3c64c3 and manufactured by Leica Instruments (Singapore) Pte Ltd. The device was registered on November 03, 2021.

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.