RF LATEX (SLIDE AGGLUTINATION METHOD) - FDA Registration dd7df2ff65136473e96dfe9947c81a6f
Access comprehensive regulatory information for RF LATEX (SLIDE AGGLUTINATION METHOD) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID dd7df2ff65136473e96dfe9947c81a6f and manufactured by BEACON DIAGNOSTICS PVT. LTD.. The device was registered on July 02, 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
dd7df2ff65136473e96dfe9947c81a6f
RF LATEX (SLIDE AGGLUTINATION METHOD)
FDA ID: dd7df2ff65136473e96dfe9947c81a6f
Device Classification
Brand Name
BEACON
Registration Information
Analysis ID
dd7df2ff65136473e96dfe9947c81a6f
Registration Date
July 02, 2022
Manufacturer
Authorized Representative

