Rapid HCV - FDA Registration 62e8d6e20de280b6332623dcf022456a
Access comprehensive regulatory information for Rapid HCV in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 62e8d6e20de280b6332623dcf022456a 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
62e8d6e20de280b6332623dcf022456a
Rapid HCV
FDA ID: 62e8d6e20de280b6332623dcf022456a
Device Classification
Brand Name
BIOLAB
Registration Information
Analysis ID
62e8d6e20de280b6332623dcf022456a
Registration Date
February 03, 2022
Manufacturer
Authorized Representative

