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Clinical Chemistry Analyzer (FUJI DRI-CHEM NX600) - FDA Registration 78132e3e208f645f5a95cb555fef081b

Access comprehensive regulatory information for Clinical Chemistry Analyzer (FUJI DRI-CHEM NX600) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 78132e3e208f645f5a95cb555fef081b and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on December 02, 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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78132e3e208f645f5a95cb555fef081b
Clinical Chemistry Analyzer (FUJI DRI-CHEM NX600)
FDA ID: 78132e3e208f645f5a95cb555fef081b
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DJ Fang

DJ Fang

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Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
78132e3e208f645f5a95cb555fef081b
Registration Date
December 02, 2022