DIAQUICK ROTA/ADENO COMBI CASSETTE - COFEPRIS Registration 1648R2018 SSA
Access comprehensive regulatory information for DIAQUICK ROTA/ADENO COMBI CASSETTE (DIAQUICK ROTA/ADENO COMBI 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 1648R2018 SSA and manufactured by INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.. The device was registered on June 28, 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 ROTA/ADENO COMBI CASSETTE ES UN DISPOSITIVO INMUNOCROMATOGRÁFICO DE FLUJO LATERAL PARA LA DETECCIÓN CUALITATIVA DE ANTÍGENOS DE ROTAVIRUS Y ADENOVIRUS EN MUESTRAS FECALES HUMANAS. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO, PARA USO EXCLUSIVO DE
THE DIAQUICK ROTA/ADENO COMBI CASSETTE IS A LATERAL FLOW IMMUNOCHROMATOGRAPHIC DEVICE FOR THE QUALITATIVE DETECTION OF ROTAVIRUS AND ADENOVIRUS ANTIGENS IN HUMAN FECAL SAMPLES. DIAGNOSTIC AGENT FOR IN VITRO USE, FOR THE EXCLUSIVE USE OF