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INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE - COFEPRIS Registration 1070R2024 SSA

Access comprehensive regulatory information for INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE (INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1070R2024 SSA and manufactured by KABLA COMERCIAL, S.A. DE C.V.. The device was registered on April 17, 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 I
1070R2024 SSA
INMUNOENSAYO DE ELECTROQUIMIOLUMINISCENC IA PARA DETERMINACIÓN CUANTITATIVA DE LA HORMONA FOLICULO ESTIMULANTE
COFEPRIS Analysis ID: 1070R2024 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
FOLLICLE-STIMULATING (ELECTROCHEMILUMINESC ENCE INMUNOASSAY) LIFOTRONIC
Trade Name (English)
FOLLICLE-STIMULATING (ELECTROCHEMILUMINESC ENCE INMUNOASSAY) LIFOTRONIC
Registration Information
Analysis ID
1070R2024 SSA
Registration Date
April 17, 2024
Manufacturer / Fabricante
Name (English)
KABLA COMERCIAL, S.A. DE C.V.