SYNCHRON CONTROL MULTILEVEL (LEVEL 1-3) COMPREHENSIVE CHEMISTRY CONTROL SERUM. - COFEPRIS Registration 2080R2019 SSA
Access comprehensive regulatory information for SYNCHRON CONTROL MULTILEVEL (LEVEL 1-3) COMPREHENSIVE CHEMISTRY CONTROL SERUM. (SYNCHRON CONTROL MULTILEVEL (LEVEL 1-3) COMPREHENSIVE CHEMISTRY CONTROL SERUM.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2080R2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on November 05, 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.
LOS CONTROLES SYNCHRON ESTÁN HECHOS DE SUERO HUMANO ESTABILIZADO Y ESTÁN DISEÑADOS PARA MONITOREAR EL RENDIMIENTO DE LOS SISTEMAS SYNCHRON EN EL LABORATORIO CLÍNICO. AGENTE DE DIAGNÓSTICO IN VITRO. PARA USO EXCLUSIVO DE LABORATORIO CLÍNICO O DE GABINETE.
SYNCHRON CONTROLS ARE MADE OF STABILIZED HUMAN SERUM AND ARE DESIGNED TO MONITOR THE PERFORMANCE OF SYNCHRON SYSTEMS IN THE CLINICAL LABORATORY. IN VITRO DIAGNOSTIC AGENT. FOR CLINICAL LABORATORY OR CABINET USE ONLY.