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PRUEBA CUALITATIVA PARA LA DETECCIÓN SIMULTÁNEA O ÚNICA DE SARS-COV-2, INFLUENZA A E INFLUENZA B MEDIANTE PCR EN TIEMPO REAL - COFEPRIS Registration 0108R2024 SSA

Access comprehensive regulatory information for PRUEBA CUALITATIVA PARA LA DETECCIÓN SIMULTÁNEA O ÚNICA DE SARS-COV-2, INFLUENZA A E INFLUENZA B MEDIANTE PCR EN TIEMPO REAL (PRUEBA CUALITATIVA PARA LA DETECCIÓN SIMULTÁNEA O ÚNICA DE SARS-COV-2, INFLUENZA A E INFLUENZA B MEDIANTE PCR EN TIEMPO REAL) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0108R2024 SSA and manufactured by ABALAT, S.A. DE C.V.. The device was registered on January 15, 2024.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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 II
0108R2024 SSA
PRUEBA CUALITATIVA PARA LA DETECCIÓN SIMULTÁNEA O ÚNICA DE SARS-COV-2, INFLUENZA A E INFLUENZA B MEDIANTE PCR EN TIEMPO REAL
COFEPRIS Analysis ID: 0108R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
ACCUPOWER® RV1 MULTIPLEX KIT
Trade Name (English)
ACCUPOWER® RV1 MULTIPLEX KIT
Registration Information
Analysis ID
0108R2024 SSA
Registration Date
January 15, 2024
Manufacturer / Fabricante
Name (Spanish)
ABALAT, S.A. DE C.V.
Name (English)
ABALAT, S.A. DE C.V.