Myanmar FDA registration e965378cfcc07412d6ce02babd44c67a

ASO LATEX (SLIDE AGGLUTINATION METHOD)

Myanmar·BEACON·BEACON DIAGNOSTICS PVT. LTD.·Registered July 02, 2022

Device classification

Brand Name: BEACON

Registration information

Analysis ID: e965378cfcc07412d6ce02babd44c67a
Registration Date: July 02, 2022

Manufacturer

Name: BEACON DIAGNOSTICS PVT. LTD.

Authorized Representative

Name: FOCUS HEALTH COMPANY LIMITED

About this record

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.