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ST-200 aQua Electrolyte Analyzer - FDA Registration 6f1cd346b6a8f16261fd68d3253fd2cf

Access comprehensive regulatory information for ST-200 aQua Electrolyte Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 6f1cd346b6a8f16261fd68d3253fd2cf and manufactured by Sensa Core Medical Instrumentation Pvt. Ltd.. The device was registered on October 03, 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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6f1cd346b6a8f16261fd68d3253fd2cf
ST-200 aQua Electrolyte Analyzer
FDA ID: 6f1cd346b6a8f16261fd68d3253fd2cf
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Device Classification
Brand Name
SENSA CORE
Registration Information
Analysis ID
6f1cd346b6a8f16261fd68d3253fd2cf
Registration Date
October 03, 2022
Authorized Representative