DIAQUICK DENGUE COMBO CASSETTE - COFEPRIS Registration 1770R2018 SSA
Access comprehensive regulatory information for DIAQUICK DENGUE COMBO CASSETTE (DIAQUICK DENGUE COMBO CASSETTE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1770R2018 SSA and manufactured by INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.. The device was registered on July 19, 2018.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
EL DIAQUICK DENGUE COMBO CASSETTE, ES UN DISPOSITIVO CUALITATIVO DE FLUJO LATERAL INMUNOCROMATOGRÁFICO, BASADO EN MEMBRANA PARA LA DETECCIÓN COMBINADA DEL ANTÍGENO DENGUE NS1 E IGG E IGM EN SANGRE HUMANA, SUERO Y PLASMA, PARA USO DIAGNÓSTICO PROFESIONAL I
THE DIAQUICK DENGUE COMBO CASSETTE, IS A QUALITATIVE IMMUNOCHROMATOGRAPHIC, MEMBRANE-BASED LATERAL FLOW DEVICE FOR THE COMBINED DETECTION OF DENGUE NS1 ANTIGEN AND IGG AND IGM IN HUMAN BLOOD, SERUM AND PLASMA, FOR PROFESSIONAL DIAGNOSTIC USE I