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Uric Acid Kit ( Uricase / PAP Method) - FDA Registration 38d751c052395ae7e511cd340186d45d

Access comprehensive regulatory information for Uric Acid Kit ( Uricase / PAP Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 38d751c052395ae7e511cd340186d45d and manufactured by Coral Clinical Systems - A Division of Tulip Diagnostics (P) Ltd.. The device was registered on June 15, 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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38d751c052395ae7e511cd340186d45d
Uric Acid Kit ( Uricase / PAP Method)
FDA ID: 38d751c052395ae7e511cd340186d45d
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Device Classification
Brand Name
Coral Clinical Systems
Registration Information
Analysis ID
38d751c052395ae7e511cd340186d45d
Registration Date
June 15, 2022