PRUEBA RÁPIDA PARA DETECCIÓN DE CREATINA QUINASA - COFEPRIS Registration 0362R2022 SSA

Access comprehensive regulatory information for PRUEBA RÁPIDA PARA DETECCIÓN DE CREATINA QUINASA (PRUEBA RÁPIDA PARA DETECCIÓN DE CREATINA QUINASA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0362R2022 SSA and manufactured by DIINSEL, S.A. DE C.V.. The device was registered on May 12, 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.