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Mycobacterium Tuberculosis DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) - FDA Registration 2ee3846d6e3efcedbd6253e0b796055e

Access comprehensive regulatory information for Mycobacterium Tuberculosis DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 2ee3846d6e3efcedbd6253e0b796055e and manufactured by Sansure Biotech Inc.. The device was registered on April 22, 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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2ee3846d6e3efcedbd6253e0b796055e
Mycobacterium Tuberculosis DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)
FDA ID: 2ee3846d6e3efcedbd6253e0b796055e
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Device Classification
Brand Name
Sansure Biotech
Registration Information
Analysis ID
2ee3846d6e3efcedbd6253e0b796055e
Registration Date
April 22, 2022
Manufacturer
Authorized Representative