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Uric Acid (UA) Kit (Uricase Method) - FDA Registration c95477b0e370ebdf764afa87d27c3e42

Access comprehensive regulatory information for Uric Acid (UA) Kit (Uricase Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c95477b0e370ebdf764afa87d27c3e42 and manufactured by Zybio Inc.. The device was registered on December 19, 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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c95477b0e370ebdf764afa87d27c3e42
Uric Acid (UA) Kit (Uricase Method)
FDA ID: c95477b0e370ebdf764afa87d27c3e42
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Device Classification
Brand Name
Zybio Inc.
Registration Information
Analysis ID
c95477b0e370ebdf764afa87d27c3e42
Registration Date
December 19, 2022
Manufacturer
Authorized Representative