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Myanmar FDA registration d775d28a61079265a3065fb1dc8c6349

Rapid Dengue Duo (NS1 Ag & IgM/IgG Ab) Test (Whole Blood/Serum/Plasma)

MyanmarADVANCED QUALITYInTec PRODUCTS, INC.Registered October 30, 2022
VerifiedFDA Myanmar · official registry
Device classification
Brand Name
ADVANCED QUALITY
Registration information
Analysis ID
d775d28a61079265a3065fb1dc8c6349
Registration Date
October 30, 2022
Manufacturer
Name
InTec PRODUCTS, INC.
Authorized Representative
Name
PASSIONCARE COMPANY LIMITED
About this record

Access comprehensive regulatory information for Rapid Dengue Duo (NS1 Ag & IgM/IgG Ab) Test (Whole Blood/Serum/Plasma) in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID d775d28a61079265a3065fb1dc8c6349 and manufactured by InTec PRODUCTS, INC.. The device was registered on October 30, 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.