FUJI DRI-CHEM NX600 - FDA Registration ac929addbd5887fb51455bc1f890da5e
Access comprehensive regulatory information for 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 ac929addbd5887fb51455bc1f890da5e 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
ac929addbd5887fb51455bc1f890da5e
FUJI DRI-CHEM NX600
FDA ID: ac929addbd5887fb51455bc1f890da5e
Device Classification
Brand Name
FUJIFILM
Registration Information
Analysis ID
ac929addbd5887fb51455bc1f890da5e
Registration Date
March 25, 2022
Manufacturer
Authorized Representative

