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Reagents used in 9180 Electrolyte Analyzer (11 Items) - FDA Registration eb3db56957a6d5352c8cb8235d716088

Access comprehensive regulatory information for Reagents used in 9180 Electrolyte Analyzer (11 Items) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID eb3db56957a6d5352c8cb8235d716088 and manufactured by Roche Diagnostics International Ltd. The device was registered on September 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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eb3db56957a6d5352c8cb8235d716088
Reagents used in 9180 Electrolyte Analyzer (11 Items)
FDA ID: eb3db56957a6d5352c8cb8235d716088
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Device Classification
Brand Name
Roche Brand
Registration Information
Analysis ID
eb3db56957a6d5352c8cb8235d716088
Registration Date
September 28, 2022
Authorized Representative