COMPLEMENT C4 (C4) DETECTION KIT (NEPHELOMETRY). - COFEPRIS Registration 2092R2019 SSA
Access comprehensive regulatory information for COMPLEMENT C4 (C4) DETECTION KIT (NEPHELOMETRY). (COMPLEMENT C4 (C4) DETECTION KIT (NEPHELOMETRY).) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2092R2019 SSA and manufactured by ATYDE MÉXICO, S.A. DE C.V.. The device was registered on November 06, 2019.
This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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.
KIT PARA DETERMINACIÓN CUANTITATIVA IN VITRO DEL CONTENIDO DE COMPLEMENTO C4 EN SUERO O PLASMA HUMANO. AGENTE DE DIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO DE LABORATORIOS CLÍNICOS O DE GABINETE
KIT FOR QUANTITATIVE IN VITRO DETERMINATION OF COMPLEMENT C4 CONTENT IN HUMAN SERUM OR PLASMA. IN VITRO DIAGNOSTIC AGENT. FOR CLINICAL OR CABINET LABORATORY USE ONLY