STANDARD™ Q DENGUE DUO TEST - INVIMA Registration 98ee58f04a8c78ffa46568d46d1e50eb
Access comprehensive regulatory information for STANDARD™ Q DENGUE DUO TEST (STANDARD™ Q DENGUE DUO TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 98ee58f04a8c78ffa46568d46d1e50eb and manufactured by QUIMIOLAB S.A.S.
This page provides complete registration details including product type (DIAGNOSTIC REAGENT), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.
LA PRUEBA STANDARD Q DENGUE DUO ES UN INMUNOENSAYO_x000D_ CROMATOGRÁFICO PARA DETECTAR LOS ANTÍGENOS NS1 DEL DENGUE_x000D_ Y LOS ANTICUERPOS IGM/IGG CONTRA EL DENGUE EN MUESTRAS DE_x000D_ SUERO, PLASMA O SANGRE COMPLETA HUMANA. ESTE KIT DE ANÁLISIS ES_x000D_ PARA USO EN UN PROCEDIMIENTO DIAGNÓSTICO IN VITRO._x000D_
THE STANDARD TEST THAT DENGUE DUO IS A INMUNOENSAYO_x000D_ CHROMATOGRAPHIC TO DETECT NS1 ANTIGENS OF DENGUE_x000D_ AND IGM/IGG ANTIBODIES AGAINST DENGUE IN SAMPLES DE_x000D_ SERUM, PLASMA, OR WHOLE HUMAN BLOOD. THIS ANALYSIS KIT ES_x000D_ FOR USE IN AN IN-VITRO._x000D_ DIAGNOSTIC PROCEDURE