Rapid Dengue Duo (NS1 Ag & IgM/IgG Ab) Test (Whole Blood/Serum/Plasma) - FDA Registration d775d28a61079265a3065fb1dc8c6349

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.