Myanmar FDA registration 5998b818a6c4688a85334727e3499d78

CRP LATEX (SLIDE AGGLUTINATION METHOD)

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

Device classification

Brand Name: BEACON

Registration information

Analysis ID: 5998b818a6c4688a85334727e3499d78
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 CRP 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 5998b818a6c4688a85334727e3499d78 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.