COULTER DXH CELL LYSE - COFEPRIS Registration 1880R2019 SSA
Access comprehensive regulatory information for COULTER DXH CELL LYSE (COULTER DXH CELL LYSE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1880R2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on September 19, 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.
AGENTE LÍTICO DE ERITROCITOS PARA LA DETERMINACIÓN CUANTITATIVA DE LA HEMOGLOBINA LA ENUMERACIÓN DE ERITROCITOS NUCLEADOS Y EL RECUENTO Y LA ESTIMACIÓN DEL TAMAÑO DE LEUCOCITOS EN LOS SISTEMAS DE ANÁLISIS CELULAR DE UNICEL DXH COULTER. UTILIZAR SOLO CON D
ERYTHROCYTE LYTIC AGENT FOR THE QUANTITATIVE DETERMINATION OF HEMOGLOBIN, NUCLEATED ERYTHROCYTE ENUMERATION AND LEUKOCYTE COUNT AND SIZE ESTIMATION IN DXH COULTER UNICEL CELL ANALYSIS SYSTEMS. USE ONLY WITH D