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Anti-Cyclic Peptide Containing Citrulline Antibody Test Kit (Rate Scattering Turbidimetric Method) - FDA Registration 90957ae161e3e1a324688f7d94beeba2

Access comprehensive regulatory information for Anti-Cyclic Peptide Containing Citrulline Antibody Test Kit (Rate Scattering Turbidimetric Method) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 90957ae161e3e1a324688f7d94beeba2 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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90957ae161e3e1a324688f7d94beeba2
Anti-Cyclic Peptide Containing Citrulline Antibody Test Kit (Rate Scattering Turbidimetric Method)
FDA ID: 90957ae161e3e1a324688f7d94beeba2
Local name: Anti-Cyclic Peptide Containing Citrulline Antibody Test Kit ๏ผˆRate Scattering Turbidimetric Method๏ผ‰
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Device Classification
Brand Name
Hiproโ„ข
Registration Information
Analysis ID
90957ae161e3e1a324688f7d94beeba2
Registration Date
October 20, 2022