Angiography System - FDA Registration 6e521c620197e61ae26edf0cedbac0c2

Access comprehensive regulatory information for Angiography System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6e521c620197e61ae26edf0cedbac0c2 and manufactured by Siemens Healthcare GmbH. The device was registered on November 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.