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SQII AUTOMATED ELISA SYSTEM - COFEPRIS Registration 715E2019 SSA

Access comprehensive regulatory information for SQII AUTOMATED ELISA SYSTEM (SQII AUTOMATED ELISA SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 715E2019 SSA and manufactured by GRIFOLS Mร‰XICO, S.A. DE C.V.. The device was registered on April 08, 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.

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COFEPRIS Official Data
Clase I
715E2019 SSA
SQII AUTOMATED ELISA SYSTEM
COFEPRIS Analysis ID: 715E2019 SSA
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Product Use / Uso del Producto
Spanish

EL SQII ES UN ANALIZADOR CON FUNCIONALIDAD ABIERTA, PARA REALIZAR UNA AMPLIA GAMA DE ANรLISIS QUรMICOS ELISA AUTOMATIZADOS.

English

THE SQII IS AN ANALYZER WITH OPEN FUNCTIONALITY, TO PERFORM A WIDE RANGE OF AUTOMATED ELISA CHEMICAL ANALYSIS.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO Mร‰DICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
LECTOR Y PROCESADOR DE ELISA
Trade Name (English)
ELISA READER AND PROCESSOR
Registration Information
Analysis ID
715E2019 SSA
Registration Date
April 08, 2019
Manufacturer / Fabricante
Name (English)
GRIFOLS Mร‰XICO, S.A. DE C.V.