Mexico COFEPRIS registration 803E2018 SSA

EQUIPO ANALIZADOR DE INMUNOENSAYOS DE QUIMIOLUMINISCENCIA

EN: CHEMOLUMINESCENCE IMMUNOASSAY ANALYZER EQUIPMENT
Mexico flagMexico·Clase I·I. MEDICAL EQUIPMENT·MINDRAY MEDICAL MÉXICO, S. DE R.L. DE C.V.·Registered March 23, 2018
Product Use / Uso del Producto
Spanish

ESTE SISTEMA ES UN ANALIZADOR DE INMUNOANÁLISIS POR QUIMIOLUMINISCENCIA PARA DIAGNÓSTICO IN-VITRO EN LABORATORIOS CLÍNICOS Y DISEÑADOS PARA LA DETERMINACIÓN IN-VITRO DE ANÁLISIS EN SUERO, PLASMA Y OTROS FLUIDOS HUMANOS.

English

THIS SYSTEM IS A CHEMILUMINESCENCE IMMUNOASSAY ANALYZER FOR IN-VITRO DIAGNOSIS IN CLINICAL LABORATORIES AND DESIGNED FOR THE IN-VITRO DETERMINATION OF ANALYSIS IN SERUM, PLASMA AND OTHER HUMAN FLUIDS.

Device classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
MINDRAY CL SERIES IMMUNOESSAY CLIA
Trade Name (English)
MINDRAY CL SERIES IMMUNOESSAY CLIA
Registration information
Analysis ID
803E2018 SSA
Registration Date
March 23, 2018
Manufacturer / Fabricante
Name (English)
MINDRAY MEDICAL MEXICO, S. DE R.L. DE C.V.
About this record

Access comprehensive regulatory information for EQUIPO ANALIZADOR DE INMUNOENSAYOS DE QUIMIOLUMINISCENCIA (CHEMOLUMINESCENCE IMMUNOASSAY ANALYZER EQUIPMENT) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 803E2018 SSA and manufactured by MINDRAY MEDICAL MÉXICO, S. DE R.L. DE C.V.. The device was registered on March 23, 2018.

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.

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