DXH 520 INSTRUMENT - COFEPRIS Registration 1825E2019 SSA
Access comprehensive regulatory information for DXH 520 INSTRUMENT (DXH 520 INSTRUMENT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1825E2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on September 09, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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.
EL DXH 520 ES UN ANALIZADOR DE HEMATOLOGÍA CUANTITATIVO DE PARÁMETROS MÚLTIPLES Y AUTOMATIZADO PARA REALIZAR DIAGNÓSTICOS IN VITRO EN LABORATORIOS CLÍNICOS, SE USA PARA IDENTIFICAR A PACIENTES NORMALES CON PARÁMETROS NORMALES GENERADOS POR EL SISTEMA DE P
THE DXH 520 IS AN AUTOMATED MULTI-PARAMETER QUANTITATIVE HEMATOLOGY ANALYZER FOR IN VITRO DIAGNOSTICS IN CLINICAL LABORATORIES, USED TO IDENTIFY NORMAL PATIENTS WITH NORMAL PARAMETERS GENERATED BY THE P