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D-Dimer Test Kit(Nephelometry immunoassay Method) - FDA Registration 82e19bef2dff0286e6b6f2a15ba8d26e

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 82e19bef2dff0286e6b6f2a15ba8d26e 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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82e19bef2dff0286e6b6f2a15ba8d26e
D-Dimer Test Kit(Nephelometry immunoassay Method)
FDA ID: 82e19bef2dff0286e6b6f2a15ba8d26e
Local name: D-Dimer Test Kit๏ผˆNephelometry immunoassay Method๏ผ‰
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Device Classification
Brand Name
Hiproโ„ข
Registration Information
Analysis ID
82e19bef2dff0286e6b6f2a15ba8d26e
Registration Date
October 20, 2022