Architect - FDA Registration a0a756edc605e7d33edd5a02962ad802

Access comprehensive regulatory information for Architect in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a0a756edc605e7d33edd5a02962ad802 and manufactured by Axis-Shield Diagnostics Limited. The device was registered on December 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.