Rheumatoid Factor (Nephelometry Immunoassay Method) - FDA Registration 748d7384039d343beb73bb9949ed88e3
Access comprehensive regulatory information for Rheumatoid Factor (Nephelometry Immunoassay Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 748d7384039d343beb73bb9949ed88e3 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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FDA Official Data
748d7384039d343beb73bb9949ed88e3
Rheumatoid Factor (Nephelometry Immunoassay Method)
FDA ID: 748d7384039d343beb73bb9949ed88e3
Device Classification
Brand Name
HIPRO
Registration Information
Analysis ID
748d7384039d343beb73bb9949ed88e3
Registration Date
December 20, 2021
Manufacturer
Authorized Representative
Name
GAMBIRO CO., LTD
