MRI System - FDA Registration be7e6766760492dee3784ab7248fc259
Access comprehensive regulatory information for MRI System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID be7e6766760492dee3784ab7248fc259 and manufactured by Siemens Shenzhen Magnetic Resonance Ltd.. The device was registered on June 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.
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FDA Official Data
be7e6766760492dee3784ab7248fc259
MRI System
FDA ID: be7e6766760492dee3784ab7248fc259
Device Classification
Brand Name
Siemens
Registration Information
Analysis ID
be7e6766760492dee3784ab7248fc259
Registration Date
June 28, 2022
Manufacturer
Authorized Representative

