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SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA SARS-COV-2 EN SUERO O PLASMA HUMANO - COFEPRIS Registration 1125R2024 SSA

Access comprehensive regulatory information for SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA SARS-COV-2 EN SUERO O PLASMA HUMANO (SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA SARS-COV-2 EN SUERO O PLASMA HUMANO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1125R2024 SSA and manufactured by INOCHEM S.A. DE C.V.. The device was registered on April 18, 2024.

This page provides complete registration details including product type (III. Agentes de diagn贸stico), 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
1125R2024 SSA
SISTEMA DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA SARS-COV-2 EN SUERO O PLASMA HUMANO
COFEPRIS Analysis ID: 1125R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. Agentes de diagn贸stico
Product Type (English)
III. Agentes de diagn贸stico
Trade Name (Spanish)
ANTI-SARS-COV-2 QUANTIVAC ELISA (1GG)
Trade Name (English)
ANTI-SARS-COV-2 QUANTIVAC ELISA (1GG)
Registration Information
Analysis ID
1125R2024 SSA
Registration Date
April 18, 2024
Manufacturer / Fabricante
Name (Spanish)
INOCHEM S.A. DE C.V.
Name (English)
INOCHEM S.A. DE C.V.