Philips Magnetic Resonance Equipment - FDA Registration 9a82971c8969aef430ee9ab39b7a5b27

Access comprehensive regulatory information for Philips Magnetic Resonance Equipment in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9a82971c8969aef430ee9ab39b7a5b27 and manufactured by Philips Medical Systems Nederland B.V.. The device was registered on April 28, 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.