D-Dimer Test Kit(Nephelometry immunoassay Method) - FDA Registration b4bcc0f6eca344d36eb0d50374f8afff
Access comprehensive regulatory information for D-Dimer 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 b4bcc0f6eca344d36eb0d50374f8afff and manufactured by Shijiazhuang Hipro Biotechnology Co.,ltd. The device was registered on October 19, 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
b4bcc0f6eca344d36eb0d50374f8afff
D-Dimer Test Kit(Nephelometry immunoassay Method)
FDA ID: b4bcc0f6eca344d36eb0d50374f8afff
Device Classification
Brand Name
Hipro
Registration Information
Analysis ID
b4bcc0f6eca344d36eb0d50374f8afff
Registration Date
October 19, 2022
Manufacturer
Authorized Representative

