Hepatitis B Virus DNA Quantitaive Fluorescence Diagnositc Kit ( PCR-Fluorescence Probing ) - FDA Registration 99e4368a02d2c13e102887e14363c1ba
Access comprehensive regulatory information for Hepatitis B Virus DNA Quantitaive Fluorescence Diagnositc 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 99e4368a02d2c13e102887e14363c1ba and manufactured by Sansure Biotech Inc.. The device was registered on March 21, 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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99e4368a02d2c13e102887e14363c1ba
Hepatitis B Virus DNA Quantitaive Fluorescence Diagnositc Kit ( PCR-Fluorescence Probing )
FDA ID: 99e4368a02d2c13e102887e14363c1ba
Device Classification
Brand Name
Sansure Biotech
Registration Information
Analysis ID
99e4368a02d2c13e102887e14363c1ba
Registration Date
March 21, 2022
Manufacturer
Authorized Representative

