Ureaplasma Urealyticum DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing) - FDA Registration 9fc580cf13f84ce2df5d58290472e9b8
Access comprehensive regulatory information for Ureaplasma Urealyticum 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 9fc580cf13f84ce2df5d58290472e9b8 and manufactured by Sansure Biotech Inc.. The device was registered on September 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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9fc580cf13f84ce2df5d58290472e9b8
Ureaplasma Urealyticum DNA Fluorescence Diagnostic Kit (PCR-Fluorescence Probing)
FDA ID: 9fc580cf13f84ce2df5d58290472e9b8
Device Classification
Brand Name
Sansure Biotech Inc.
Registration Information
Analysis ID
9fc580cf13f84ce2df5d58290472e9b8
Registration Date
September 21, 2022
Manufacturer
Authorized Representative

