Leica Microsystems-M220 - FDA Registration 91738e65c8de83f64095ad5b5f2e3292

Access comprehensive regulatory information for Leica Microsystems-M220 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 91738e65c8de83f64095ad5b5f2e3292 and manufactured by Leica Instruments (Singapore) Pte Ltd. The device was registered on April 29, 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.