Syphilis TPHA Liquid - FDA Registration cb0e44b7193c6f1cc0eb88c775ce0d93
Access comprehensive regulatory information for Syphilis TPHA Liquid in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID cb0e44b7193c6f1cc0eb88c775ce0d93 and manufactured by Gesellschaft fรผr Biochemica und Diagnostica mbH. The device was registered on December 06, 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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FDA Official Data
cb0e44b7193c6f1cc0eb88c775ce0d93
Syphilis TPHA Liquid
FDA ID: cb0e44b7193c6f1cc0eb88c775ce0d93
Device Classification
Brand Name
Human
Registration Information
Analysis ID
cb0e44b7193c6f1cc0eb88c775ce0d93
Registration Date
December 06, 2022
Manufacturer
Authorized Representative

