DIAQUICK RUBELLA IGM CASSETTE - COFEPRIS Registration 1771R2018 SSA
Access comprehensive regulatory information for DIAQUICK RUBELLA IGM CASSETTE (DIAQUICK RUBELLA IGM 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 1771R2018 SSA and manufactured by INVESTIGACIÓN DIAGNÓSTICA, S.A. DE C.V.. The device was registered on July 19, 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 RUBELLA IGM CASSETTE, ES UN INMUNOENSAYO CROMATOGRÁFICO DE FLUJO LATERAL PARA LA DETECCIÓN CUALITATIVA DE ANTICUERPOS IGM CONTRA EL VIRUS DE LA RUBÉOLA EN SUERO O PLASMA HUMANO PARA AYUDAR EN EL DIAGNÓSTICO DE LA INFECCIÓN POR RUBEOLA. AGENTE
THE DIAQUICK RUBELLA IGM CASSETTE IS A LATERAL FLOW CHROMATOGRAPHIC IMMUNOASSAY FOR THE QUALITATIVE DETECTION OF IGM ANTIBODIES AGAINST RUBELLA VIRUS IN HUMAN SERUM OR PLASMA TO AID IN THE DIAGNOSIS OF RUBELLA INFECTION. AGENT