PRUEBA RÁPIDA DE TRICHOMONAS VAGINALIS EN CASETE - COFEPRIS Registration 1858R2024 SSA

Access comprehensive regulatory information for PRUEBA RÁPIDA DE TRICHOMONAS VAGINALIS EN CASETE (PRUEBA RÁPIDA DE TRICHOMONAS VAGINALIS EN CASETE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1858R2024 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on July 02, 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.