FTD ZIKA/DENGUE/CHIK - COFEPRIS Registration 289R2019 SSA
Access comprehensive regulatory information for FTD ZIKA/DENGUE/CHIK (FTD ZIKA/DENGUE/CHIK) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 289R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on February 14, 2019.
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.
FTD ZIKA/DENGUE/CHIK ES UNA PRUEBA IN VITRO PARA LA DETECCIÓN CUALITATIVA DE ÁCIDO NUCLEICO VÍRICO COMO UNA AYUDA PARA LA EVALUACIÓN DE INFECCIONES POR EL VIRUS DEL ZIKA, EL VIRUS DEL DENGUE Y EL VIRUS DE LA CHIKUNGUÑA. AGENTE DE DIAGNÓSTICO. PARA USO
FTD ZIKA/DENGUE/CHIK IS AN IN VITRO TEST FOR THE QUALITATIVE DETECTION OF VIRAL NUCLEIC ACID AS AN AID TO THE EVALUATION OF ZIKA VIRUS, DENGUE VIRUS, AND CHIKUNGUNYA VIRUS INFECTIONS. DIAGNOSTIC AGENT. FOR USE