Abbott Architect - FDA Registration 0ca8bfe8264ce9aa80f7ea67d53c4751

Access comprehensive regulatory information for Abbott Architect in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0ca8bfe8264ce9aa80f7ea67d53c4751 and manufactured by Abbott Ireland Diagnostics Division. The device was registered on July 01, 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.