LUPINE BR Anchor - FDA Registration fa3f9ed549824869b0962f3c8fba49f0

Access comprehensive regulatory information for LUPINE BR Anchor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID fa3f9ed549824869b0962f3c8fba49f0 and manufactured by Medos SARL. The device was registered on December 07, 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.