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LIAISON® MDX - COFEPRIS Registration 121E2019 SSA

Access comprehensive regulatory information for LIAISON® MDX (LIAISON® MDX) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 121E2019 SSA and manufactured by DIASORIN MÉXICO S.A. DE C.V.. The device was registered on January 29, 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
121E2019 SSA
LIAISON® MDX
COFEPRIS Analysis ID: 121E2019 SSA
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Product Use / Uso del Producto
Spanish

EL LIAISON® MDX ES UN TERMOCICLADOR PARA REACCIÓN EN CADENA DE LA POLIMERASA (PCR) EN TIEMPO REAL EN FORMA RÁPIDA, QUE SE UTILIZA PARA LA IDENTIFICACIÓN DE ÁCIDO NUCLEICO A PARTIR DE MUESTRAS BIOLÓGICAS. EL EQUIPO UTILIZA MEDIOS EN FORMATO DE DISCOS PARA

English

THE LIAISON® MDX IS A RAPID REAL-TIME POLYMERASE CHAIN REACTION (PCR) THERMAL CYCLER USED FOR NUCLEIC ACID IDENTIFICATION FROM BIOLOGICAL SAMPLES. THE COMPUTER USES MEDIA IN DISK FORMAT TO

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
TERMOCICLADOR PARA REACCIÓN EN CADENA DE LA POLIMERASA (PCR) EN TIEMPO REAL
Trade Name (English)
THERMAL CYCLER FOR REAL-TIME POLYMERASE CHAIN REACTION (PCR)
Registration Information
Analysis ID
121E2019 SSA
Registration Date
January 29, 2019
Manufacturer / Fabricante
Name (English)
DIASORIN MEXICO S.A. DE C.V.