Myanmar FDA registration a1847dc28aa7de149e7a4f72fdf703e3
Magnesium
Device classification
- Brand Name
- Abbott
Registration information
- Analysis ID
- a1847dc28aa7de149e7a4f72fdf703e3
- Registration Date
- January 19, 2022
Manufacturer
Authorized Representative
About this record
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.
Free DatabasePowered by Pure Global AIFDA Official Data