HBsAg rapid tests - FDA Registration 379f5a0fba6faebe73742297cc28ee83
Access comprehensive regulatory information for HBsAg rapid tests in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 379f5a0fba6faebe73742297cc28ee83 and manufactured by Zhejiang Orient Gene Biotech Co.,ltd. The device was registered on September 08, 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
379f5a0fba6faebe73742297cc28ee83
HBsAg rapid tests
FDA ID: 379f5a0fba6faebe73742297cc28ee83
Device Classification
Brand Name
DIAGNOSTAR
Registration Information
Analysis ID
379f5a0fba6faebe73742297cc28ee83
Registration Date
September 08, 2022
Manufacturer
Authorized Representative

