CERTEST H. pylori - FDA Registration b00b25664544dc056a8aadf6b3058770
Access comprehensive regulatory information for CERTEST H. pylori in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b00b25664544dc056a8aadf6b3058770 and manufactured by CERTEST BIOTEC S.L.. The device was registered on March 21, 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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FDA Official Data
b00b25664544dc056a8aadf6b3058770
CERTEST H. pylori
FDA ID: b00b25664544dc056a8aadf6b3058770
Device Classification
Brand Name
CERTEST BIOTEC S.L.
Registration Information
Analysis ID
b00b25664544dc056a8aadf6b3058770
Registration Date
March 21, 2022
Manufacturer
Authorized Representative

