HIV 1.2.O Rapid Test Cassette - FDA Registration b091ef6b7d3e0e467b273f5ef249df11
Access comprehensive regulatory information for HIV 1.2.O Rapid Test Cassette in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b091ef6b7d3e0e467b273f5ef249df11 and manufactured by Hangzhou Biotest Biotech Co., Ltd.. The device was registered on January 18, 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
b091ef6b7d3e0e467b273f5ef249df11
HIV 1.2.O Rapid Test Cassette
FDA ID: b091ef6b7d3e0e467b273f5ef249df11
Device Classification
Brand Name
RightSign
Registration Information
Analysis ID
b091ef6b7d3e0e467b273f5ef249df11
Registration Date
January 18, 2022
Manufacturer
Authorized Representative

