STROMATOLYSER™-NR REACTIVO LISANTE - COFEPRIS Registration 2237R2019 SSA
Access comprehensive regulatory information for STROMATOLYSER™-NR REACTIVO LISANTE (STROMATOLYSER-NR™ LYSING REAGENT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2237R2019 SSA and manufactured by SYSMEX DIAGNÓSTICOS MÉXICO, S. DE R.L. DE C.V.. The device was registered on December 10, 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.
SE UTILIZA PARA DILUIR, LISAR Y TEÑIR LAS CÉLULAS NUCLEADAS PARA EL ANÁLISIS DE RECUENTO DE RETICULOCITOS DE NRBC Y EL PORCENTAJE DE NRBC EN SANGRE CON ANALIZADORES DE HEMATOLOGÍA AUTOMATIZADOS DE SYSMEX ESPECÍFICOS. AGENTE DE DIAGNÓSTICO PARA USO IN VIT
IT IS USED TO DILUTE, LYSE AND STAIN NUCLEATED CELLS FOR ANALYSIS OF NRBC RETICULOCYTE COUNT AND BLOOD NRBC PERCENTAGE WITH SPECIFIC SYSMEX AUTOMATED HEMATOLOGY ANALYZERS. DIAGNOSTIC AGENT FOR USE IN VIT