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Processor - FDA Registration 4a876110c31257ab861f06f31c85b33a

Access comprehensive regulatory information for Processor in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4a876110c31257ab861f06f31c85b33a and manufactured by FUJIFILM Healthcare Manufacturing Coroporation Hanamaki Office. 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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FDA Official Data
4a876110c31257ab861f06f31c85b33a
Processor
FDA ID: 4a876110c31257ab861f06f31c85b33a
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Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
4a876110c31257ab861f06f31c85b33a
Registration Date
September 28, 2022