Human Immunodeficiency Virus Type 1 RNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) - FDA Registration 2da450407916d3c5432ac079960688ca
Access comprehensive regulatory information for Human Immunodeficiency Virus Type 1 RNA Quantitative 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 2da450407916d3c5432ac079960688ca and manufactured by Sansure Biotech Inc.. The device was registered on October 11, 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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2da450407916d3c5432ac079960688ca
Human Immunodeficiency Virus Type 1 RNA Quantitative Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)
FDA ID: 2da450407916d3c5432ac079960688ca
Device Classification
Brand Name
Sansure Biotech Inc.
Registration Information
Analysis ID
2da450407916d3c5432ac079960688ca
Registration Date
October 11, 2022
Manufacturer
Authorized Representative

