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ALINITY I EBV VCA IGM - COFEPRIS Registration 2262R2018 SSA

Access comprehensive regulatory information for ALINITY I EBV VCA IGM (ALINITY I EBV VCA IGM) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2262R2018 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on September 26, 2018.

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.

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COFEPRIS Official Data
Clase I
2262R2018 SSA
ALINITY I EBV VCA IGM
COFEPRIS Analysis ID: 2262R2018 SSA
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Product Use / Uso del Producto
Spanish

ENSAYO PARA LA DETECCIร“N DE ANTICUERPOS IGM FRENTE AL ANTรGENO DE LA CรPSIDE (VCA, VIRAL CAPSID ANTIGEN) DEL VIRUS EPSTEIN-BARR (VEB)

English

ASSAY FOR THE DETECTION OF IGM ANTIBODIES AGAINST CAPSID ANTIGEN (VCA, VIRAL CAPSID ANTIGEN) OF EPSTEIN-BARR VIRUS (EVB)

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
ENSAYO PARA LA DETECCIร“N DE ANTICUERPOS IGM FRENTE AL ANTรGENO DE LA CรPSIDE (VCA, VIRAL CAPSID ANTI
Trade Name (English)
ASSAY FOR THE DETECTION OF IGM ANTIBODIES AGAINST CAPSID ANTIGEN (VCA, VIRAL CAPSID ANTI
Registration Information
Analysis ID
2262R2018 SSA
Registration Date
September 26, 2018
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MEXICO SA DE CV