FLOW CHECK™ FLUOROESFERAS - COFEPRIS Registration 1910R2019 SSA
Access comprehensive regulatory information for FLOW CHECK™ FLUOROESFERAS (FLOW CHECK™ FLUOROESFERAS) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1910R2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on September 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.
LAS FLUOROESFERAS FLOW-CHECK SON UNA SUSPENSIÓN DE MICROESFERAS FLUORESCENTES QUE SE UTILIZAN PARA LA VERIFICACIÓN DIARIA DEL SISTEMA DE FLUIDEZ Y ALINEACIÓN ÓPTICA DEL CITÓMETRO DE FLUJO, CITIOS, NAVIOS EX O CYTOMICS. AGENTE DE DIAGNÓSTICO PARA USO IN V
FLOW-CHECK FLUOROSPHERES ARE A SUSPENSION OF FLUORESCENT MICROSPHERES THAT ARE USED FOR THE DAILY VERIFICATION OF THE FLOW SYSTEM AND OPTICAL ALIGNMENT OF THE FLOW CYTOMETER, CITIOS, NAVIOS EX OR CYTOMICS. DIAGNOSTIC AGENT FOR IN V USE