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PRUEBA RÁPIDA PARA LA DETECCIÓN DE ANTICUERPOS CONTRA EL SARS-COV-2 - COFEPRIS Registration 0617R2024 SSA

Access comprehensive regulatory information for PRUEBA RÁPIDA PARA LA DETECCIÓN DE ANTICUERPOS CONTRA EL SARS-COV-2 (PRUEBA RÁPIDA PARA LA DETECCIÓN DE ANTICUERPOS CONTRA EL SARS-COV-2) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0617R2024 SSA and manufactured by PRODUCTOS ROCHE, S.A. DE C.V.. The device was registered on March 05, 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
0617R2024 SSA
PRUEBA RÁPIDA PARA LA DETECCIÓN DE ANTICUERPOS CONTRA EL SARS-COV-2
COFEPRIS Analysis ID: 0617R2024 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)
SARS-COV-2 RAPID ANTIBODY TEST
Trade Name (English)
SARS-COV-2 RAPID ANTIBODY TEST
Registration Information
Analysis ID
0617R2024 SSA
Registration Date
March 05, 2024
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DE C.V.