Pure Global

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.

Free Database
Powered by Pure Global AI
FDA Official Data
68a89f0efe785e3be2ba5f13d788bfd6
Truelab® One Dx
FDA ID: 68a89f0efe785e3be2ba5f13d788bfd6
Local name: Truelab® Uno Dx
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Classification
Brand Name
Molbio
Registration Information
Analysis ID
68a89f0efe785e3be2ba5f13d788bfd6
Registration Date
August 09, 2022