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MAGNESIUM (Mg) - FDA Registration 69d611faf03085206ea08255fb479483

Access comprehensive regulatory information for MAGNESIUM (Mg) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 69d611faf03085206ea08255fb479483 and manufactured by Randox Laboratories Ltd.. 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.

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69d611faf03085206ea08255fb479483
MAGNESIUM (Mg)
FDA ID: 69d611faf03085206ea08255fb479483
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Device Classification
Brand Name
Randox
Registration Information
Analysis ID
69d611faf03085206ea08255fb479483
Registration Date
April 28, 2022
Manufacturer
Authorized Representative