Magnesium - FDA Registration a1847dc28aa7de149e7a4f72fdf703e3
Access comprehensive regulatory information for Magnesium in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID a1847dc28aa7de149e7a4f72fdf703e3 and manufactured by Abbott Ireland Diagnostics Division. The device was registered on January 19, 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
a1847dc28aa7de149e7a4f72fdf703e3
Magnesium
FDA ID: a1847dc28aa7de149e7a4f72fdf703e3
Device Classification
Brand Name
Abbott
Registration Information
Analysis ID
a1847dc28aa7de149e7a4f72fdf703e3
Registration Date
January 19, 2022
Manufacturer
Authorized Representative

