H360 Hematology Analyser - FDA Registration 8c90e4305b981220d58ce96efae7e76b

Access comprehensive regulatory information for H360 Hematology Analyser in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 8c90e4305b981220d58ce96efae7e76b and manufactured by Erba Lachema s.r.o. The device was registered on May 18, 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.