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Alpha-Fetoprotein Test Kit ( Nephelometry immunoassay Method) - FDA Registration b712a73c6b3e687d8f98110fc73f98ec

Access comprehensive regulatory information for Alpha-Fetoprotein Test Kit ( Nephelometry immunoassay Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID b712a73c6b3e687d8f98110fc73f98ec and manufactured by Shijiazhuang Hipro Biotechnology Co.,Ltd. The device was registered on December 20, 2021.

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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b712a73c6b3e687d8f98110fc73f98ec
Alpha-Fetoprotein Test Kit ( Nephelometry immunoassay Method)
FDA ID: b712a73c6b3e687d8f98110fc73f98ec
Local name: Alpha-Fetoprotein Test Kit ๏ผˆ Nephelometry immunoassay Method๏ผ‰
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Device Classification
Brand Name
HIPRO
Registration Information
Analysis ID
b712a73c6b3e687d8f98110fc73f98ec
Registration Date
December 20, 2021
Authorized Representative