REACTIVO PARA PRUEBA DE PROTEÍNA C REACTIVA (CRP) - COFEPRIS Registration 0027R2024 SSA

Access comprehensive regulatory information for REACTIVO PARA PRUEBA DE PROTEÍNA C REACTIVA (CRP) (REACTIVO PARA PRUEBA DE PROTEÍNA C REACTIVA (CRP)) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0027R2024 SSA and manufactured by KANA UNDESA, S.A. DE C.V.. The device was registered on January 08, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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.