STANDARD™Q DENGUE NS1 AG TEST - INVIMA Registration 25caf32a9c20c5fe4048294027345ed4
Access comprehensive regulatory information for STANDARD™Q DENGUE NS1 AG TEST (STANDARD™Q DENGUE NS1 AG TEST) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 25caf32a9c20c5fe4048294027345ed4 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 NS1 AG ES UN INMUNOENSAYO _x000D_ CROMATOGRÁFICO PARA DETECTAR LOS ANTÍGENOS NS1 EN MUESTRAS _x000D_ DE SANGRE HUMANA. ESTE KIT DE ANÁLISIS ES PARA USO EN UN _x000D_ PROCEDIMIENTO DIAGNÓSTICO IN VITRO.
THE STANDARD Q DENGUE NS1 AG TEST IS AN IMMUNOASSAY _x000D_ CHROMATOGRAPHIC FOR DETECTING NS1 ANTIGENS IN SAMPLES _x000D_ OF HUMAN BLOOD. THIS TEST KIT IS FOR USE IN A _x000D_ IN VITRO DIAGNOSTIC PROCEDURE.