PRUEBA RÁPIDA PARA LA DETECCIÓN DE GONADOTROPINA CORIÓNICA HUMANA. - COFEPRIS Registration 1450R2022 SSA

Access comprehensive regulatory information for PRUEBA RÁPIDA PARA LA DETECCIÓN DE GONADOTROPINA CORIÓNICA HUMANA. (PRUEBA RÁPIDA PARA LA DETECCIÓN DE GONADOTROPINA CORIÓNICA HUMANA.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1450R2022 SSA and manufactured by DIAGMEX, S.A. DE C.V.. The device was registered on November 22, 2022.

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.