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Clinical Chemistry Analyzer - FDA Registration 46ac5bb5ae5d6d89c3d4eb442fbdfb34

Access comprehensive regulatory information for Clinical Chemistry Analyzer in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 46ac5bb5ae5d6d89c3d4eb442fbdfb34 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. The device was registered on March 25, 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
46ac5bb5ae5d6d89c3d4eb442fbdfb34
Clinical Chemistry Analyzer
FDA ID: 46ac5bb5ae5d6d89c3d4eb442fbdfb34
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DJ Fang

DJ Fang

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Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
46ac5bb5ae5d6d89c3d4eb442fbdfb34
Registration Date
March 25, 2022