Electrolyte Testing System - FDA Registration 9ad109ee58890425f97c3aee7bc113be
Access comprehensive regulatory information for Electrolyte Testing System in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 9ad109ee58890425f97c3aee7bc113be and manufactured by Diamond Diagnostic Inc. The device was registered on October 12, 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
9ad109ee58890425f97c3aee7bc113be
Electrolyte Testing System
FDA ID: 9ad109ee58890425f97c3aee7bc113be
Device Classification
Brand Name
Diamond
Registration Information
Analysis ID
9ad109ee58890425f97c3aee7bc113be
Registration Date
October 12, 2022
Manufacturer
Authorized Representative

