ASO LATEX (SLIDE AGGLUTINATION METHOD) - FDA Registration e965378cfcc07412d6ce02babd44c67a
Access comprehensive regulatory information for ASO 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 e965378cfcc07412d6ce02babd44c67a 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
e965378cfcc07412d6ce02babd44c67a
ASO LATEX (SLIDE AGGLUTINATION METHOD)
FDA ID: e965378cfcc07412d6ce02babd44c67a
Device Classification
Brand Name
BEACON
Registration Information
Analysis ID
e965378cfcc07412d6ce02babd44c67a
Registration Date
July 02, 2022
Manufacturer
Authorized Representative

