Rapid HIV 1 & 2 - FDA Registration 148d29d29e1427f8bd01df79fd26f128
Access comprehensive regulatory information for Rapid HIV 1 & 2 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 148d29d29e1427f8bd01df79fd26f128 and manufactured by BIOLAB DIAGNOSTICS (I) PVT.LTD.. The device was registered on February 03, 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
148d29d29e1427f8bd01df79fd26f128
Rapid HIV 1 & 2
FDA ID: 148d29d29e1427f8bd01df79fd26f128
Device Classification
Brand Name
BIOLAB
Registration Information
Analysis ID
148d29d29e1427f8bd01df79fd26f128
Registration Date
February 03, 2022
Manufacturer
Authorized Representative

