REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE AMONIACO EN PLASMA HUMANO - COFEPRIS Registration 1841R2024 SSA

Access comprehensive regulatory information for REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE AMONIACO EN PLASMA HUMANO (REACTIVO PARA LA DETERMINACIÓN CUANTITATIVA DE AMONIACO EN PLASMA HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1841R2024 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on July 01, 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.