CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC - COFEPRIS Registration 1941R2019 SSA
Access comprehensive regulatory information for CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC (CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1941R2019 SSA and manufactured by BECKMAN COULTER DE MÉXICO, S.A. DE C.V.. The device was registered on October 04, 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.
CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC ESTÁ DISEÑADO PARA SER UTILIZADO POR PROFESIONALES CAPACITADOS EN UN ENTORNO DE LABORATORIO CLÍNICO CON FINES DE DIAGNÓSTICO. CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC ES UN REACTIVO FLUORESCENTE DUAL COMPUESTO
CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC IS DESIGNED TO BE USED BY TRAINED PROFESSIONALS IN A CLINICAL LABORATORY SETTING FOR DIAGNOSTIC PURPOSES. CYTO-STAT®/COULTER CLONE® T11-RD1/B1-FITC IS A COMPOSITE DUAL FLUORESCENT REAGENT

