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High Density Lipoprotein Cholesterol Test Kit (Enzymic Method) - FDA Registration 123a9fe6786694c746224d873a2a5d09

Access comprehensive regulatory information for High Density Lipoprotein Cholesterol Test Kit (Enzymic Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 123a9fe6786694c746224d873a2a5d09 and manufactured by Shijiazhuang Hipro Biotechnology Co.,ltd. The device was registered on October 20, 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
123a9fe6786694c746224d873a2a5d09
High Density Lipoprotein Cholesterol Test Kit (Enzymic Method)
FDA ID: 123a9fe6786694c746224d873a2a5d09
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DJ Fang

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Device Classification
Brand Name
Hiproโ„ข
Registration Information
Analysis ID
123a9fe6786694c746224d873a2a5d09
Registration Date
October 20, 2022