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Albumin Kit (BCG Method) - FDA Registration 2c8ba11b7a5af5b92384371bb7033dd1

Access comprehensive regulatory information for Albumin Kit (BCG Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2c8ba11b7a5af5b92384371bb7033dd1 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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2c8ba11b7a5af5b92384371bb7033dd1
Albumin Kit (BCG Method)
FDA ID: 2c8ba11b7a5af5b92384371bb7033dd1
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Device Classification
Brand Name
Coral Clinical Systems
Registration Information
Analysis ID
2c8ba11b7a5af5b92384371bb7033dd1
Registration Date
June 15, 2022