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KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA EL VIRUS DE LA RUBÉOLA EN SUERO O PLASMA HUMANO - COFEPRIS Registration 1670R2022 SSA

Access comprehensive regulatory information for KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA EL VIRUS DE LA RUBÉOLA EN SUERO O PLASMA HUMANO (KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA EL VIRUS DE LA RUBÉOLA 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 1670R2022 SSA and manufactured by INOCHEM S.A. DE C.V.. The device was registered on December 15, 2022.

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
1670R2022 SSA
KIT DE PRUEBA PARA DETERMINACIONES IN VITRO (IVD) DE ANTICUERPOS CONTRA EL VIRUS DE LA RUBÉOLA EN SUERO O PLASMA HUMANO
COFEPRIS Analysis ID: 1670R2022 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)
AVIDITY: ANTI-RUBELLA VIRUS ELISA (IGG).
Trade Name (English)
AVIDITY: ANTI-RUBELLA VIRUS ELISA (IGG).
Registration Information
Analysis ID
1670R2022 SSA
Registration Date
December 15, 2022
Manufacturer / Fabricante
Name (Spanish)
INOCHEM S.A. DE C.V.
Name (English)
INOCHEM S.A. DE C.V.