Trueprep® AUTO v2 - FDA Registration c9f66fd3097adb7c50b7ce98e5f3232e
Access comprehensive regulatory information for Trueprep® AUTO v2 in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID c9f66fd3097adb7c50b7ce98e5f3232e and manufactured by MOLBIO DIAGNOSTICS PVT. LTD. The device was registered on August 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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FDA Official Data
c9f66fd3097adb7c50b7ce98e5f3232e
Trueprep® AUTO v2
FDA ID: c9f66fd3097adb7c50b7ce98e5f3232e
Device Classification
Brand Name
Molbio
Registration Information
Analysis ID
c9f66fd3097adb7c50b7ce98e5f3232e
Registration Date
August 11, 2022
Manufacturer
Authorized Representative

