COMPLEMENT C3 (C3) DETECTION KIT (NEPHELOMETRY) - COFEPRIS Registration 2189R2019 SSA
Access comprehensive regulatory information for COMPLEMENT C3 (C3) DETECTION KIT (NEPHELOMETRY) (COMPLEMENT C3 (C3) 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 2189R2019 SSA and manufactured by ATYDE MÉXICO S.A. DE C.V.. The device was registered on November 26, 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 C3 EN SUERO O PLASMA HUMANO. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETES.
KIT FOR QUANTITATIVE IN VITRO DETERMINATION OF COMPLEMENT C3 CONTENT IN HUMAN SERUM OR PLASMA. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.