Myanmar FDA registration dd7df2ff65136473e96dfe9947c81a6f

RF LATEX (SLIDE AGGLUTINATION METHOD)

Name: RF LATEX (SLIDE AGGLUTINATION METHOD) — Myanmar FDA registration dd7df2ff65136473e96dfe9947c81a6f
Creator: BEACON DIAGNOSTICS PVT. LTD.
Keywords: RF LATEX (SLIDE AGGLUTINATION METHOD), RF LATEX (SLIDE AGGLUTINATION METHOD), BEACON, dd7df2ff65136473e96dfe9947c81a6f, Myanmar FDA registration

MyanmarBEACONBEACON DIAGNOSTICS PVT. LTD.Registered July 02, 2022

VerifiedFDA Myanmar · official registry

Device classification

Brand Name: BEACON

Registration information

Analysis ID: dd7df2ff65136473e96dfe9947c81a6f
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 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.