Truelab® One Dx - FDA Registration 68a89f0efe785e3be2ba5f13d788bfd6
Access comprehensive regulatory information for Truelab® One Dx in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 68a89f0efe785e3be2ba5f13d788bfd6 and manufactured by MOLBIO DIAGNOSTICS PVT. LTD. The device was registered on August 09, 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
68a89f0efe785e3be2ba5f13d788bfd6
Truelab® One Dx
FDA ID: 68a89f0efe785e3be2ba5f13d788bfd6
Local name: Truelab® Uno Dx
Device Classification
Brand Name
Molbio
Registration Information
Analysis ID
68a89f0efe785e3be2ba5f13d788bfd6
Registration Date
August 09, 2022
Manufacturer
Authorized Representative

