PRUEBA RÁPIDA COMBINADA DE INFLUENZA A Y B. - COFEPRIS Registration 491R2018 SSA
Access comprehensive regulatory information for PRUEBA RÁPIDA COMBINADA DE INFLUENZA A Y B. (COMBINED RAPID INFLUENZA A AND B TEST.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 491R2018 SSA and manufactured by AMUNET, S.A. DE C.V.. The device was registered on February 21, 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.
PRUEBA RÁPIDA INMUNOCROMATOGRÁFICA PARA LA DETERMINACIÓN CUALITATIVA Y DIFERENCIACIÓN DE ANTÍGENOS DEL VIRUS DE LA INFLUENZA TIPO A Y B, A PARTIR DE MUESTRAS NASALES Y NASOFARÍNGEAS.
RAPID IMMUNOCHROMATOGRAPHIC TEST FOR THE QUALITATIVE DETERMINATION AND DIFFERENTIATION OF INFLUENZA VIRUS ANTIGENS TYPE A AND B, FROM NASAL AND NASOPHARYNGEAL SAMPLES.