Mexico COFEPRIS registration 0780R2024 SSA

INMUNOENSAYO DE CA 15-3 EN SUERO O PLASMA HUMANO.

EN: INMUNOENSAYO DE CA 15-3 EN SUERO O PLASMA HUMANO.
Mexico flagMexico·Clase II·III. Agentes de diagnóstico·INOCHEM S.A. DE C.V.·Registered March 22, 2024
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)
CA 15-3 ELISA DIA.METRA
Trade Name (English)
CA 15-3 ELISA DIA.METRA
Registration information
Analysis ID
0780R2024 SSA
Registration Date
March 22, 2024
Manufacturer / Fabricante
Name (Spanish)
INOCHEM S.A. DE C.V.
Name (English)
INOCHEM S.A. DE C.V.
About this record

Access comprehensive regulatory information for INMUNOENSAYO DE CA 15-3 EN SUERO O PLASMA HUMANO. (INMUNOENSAYO DE CA 15-3 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 0780R2024 SSA and manufactured by INOCHEM S.A. DE C.V.. The device was registered on March 22, 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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