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Glycohemoglobin Test Kit( Nephelometry immunoassay Method) - FDA Registration 9f16d627d7e1cb98f5d460184b8a9379

Access comprehensive regulatory information for Glycohemoglobin 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 9f16d627d7e1cb98f5d460184b8a9379 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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9f16d627d7e1cb98f5d460184b8a9379
Glycohemoglobin Test Kit( Nephelometry immunoassay Method)
FDA ID: 9f16d627d7e1cb98f5d460184b8a9379
Local name: Glycohemoglobin Test Kit๏ผˆ Nephelometry immunoassay Method๏ผ‰
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Device Classification
Brand Name
HIPRO
Registration Information
Analysis ID
9f16d627d7e1cb98f5d460184b8a9379
Registration Date
December 20, 2021
Authorized Representative