Truelab® Quattro - FDA Registration 243ba6fe62395bfa01049d77fcecf490
Access comprehensive regulatory information for Truelab® Quattro in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID 243ba6fe62395bfa01049d77fcecf490 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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243ba6fe62395bfa01049d77fcecf490
Truelab® Quattro
FDA ID: 243ba6fe62395bfa01049d77fcecf490
Device Classification
Brand Name
Molbio
Registration Information
Analysis ID
243ba6fe62395bfa01049d77fcecf490
Registration Date
August 11, 2022
Manufacturer
Authorized Representative

