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H. Pylori Ab Combo Rapid Test - FDA Registration 4b331f374b13df35936cc1f2b4af240a

Access comprehensive regulatory information for H. Pylori Ab Combo Rapid Test in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 4b331f374b13df35936cc1f2b4af240a and manufactured by CTK Biotech, Inc.. The device was registered on February 26, 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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4b331f374b13df35936cc1f2b4af240a
H. Pylori Ab Combo Rapid Test
FDA ID: 4b331f374b13df35936cc1f2b4af240a
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Device Classification
Brand Name
Aria Brand
Registration Information
Analysis ID
4b331f374b13df35936cc1f2b4af240a
Registration Date
February 26, 2022
Manufacturer
Authorized Representative