COVID-19 Antigen Rapid Test Cassette - FDA Registration 804d08966c8ae9a1915ef1da58dfd76e
Access comprehensive regulatory information for COVID-19 Antigen Rapid Test Cassette in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 804d08966c8ae9a1915ef1da58dfd76e and manufactured by Hangzhou Clongene Biotech Co., Ltd.. The device was registered on February 28, 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
804d08966c8ae9a1915ef1da58dfd76e
COVID-19 Antigen Rapid Test Cassette
FDA ID: 804d08966c8ae9a1915ef1da58dfd76e
Device Classification
Brand Name
CLUNGENE
Registration Information
Analysis ID
804d08966c8ae9a1915ef1da58dfd76e
Registration Date
February 28, 2022
Manufacturer
Authorized Representative

