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BRIZIO Hemoconcentrator - FDA Registration f1c95fca884246135a0990c4b0531939

Access comprehensive regulatory information for BRIZIO Hemoconcentrator in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID f1c95fca884246135a0990c4b0531939 and manufactured by Nipro Corporation Odate Factory. The device was registered on December 29, 2021.

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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f1c95fca884246135a0990c4b0531939
BRIZIO Hemoconcentrator
FDA ID: f1c95fca884246135a0990c4b0531939
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Device Classification
Brand Name
NIPRO
Registration Information
Analysis ID
f1c95fca884246135a0990c4b0531939
Registration Date
December 29, 2021
Authorized Representative