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Reagent - FDA Registration 0c480e3eb3b602dabb8e5d414d4212e7

Access comprehensive regulatory information for Reagent in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 0c480e3eb3b602dabb8e5d414d4212e7 and manufactured by HORIBA ABX SAS. The device was registered on December 14, 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
0c480e3eb3b602dabb8e5d414d4212e7
Reagent
FDA ID: 0c480e3eb3b602dabb8e5d414d4212e7
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Device Classification
Brand Name
HORIBA
Registration Information
Analysis ID
0c480e3eb3b602dabb8e5d414d4212e7
Registration Date
December 14, 2022
Manufacturer
Authorized Representative