Mexico COFEPRIS registration 0577R2024 SSA

REACTIVO Y CONTROLES PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA.

EN: REACTIVO Y CONTROLES PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA.
Mexico flagMexico·Clase I·III. Agentes de diagnóstico·CORPORINTER, S.A. DE C.V.·Registered February 21, 2024
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)
FRT-CHECK-1.
Trade Name (English)
FRT-CHECK-1.
Registration information
Analysis ID
0577R2024 SSA
Registration Date
February 21, 2024
Manufacturer / Fabricante
Name (English)
CORPORINTER, S.A. DE C.V.
About this record

Access comprehensive regulatory information for REACTIVO Y CONTROLES PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA. (REACTIVO Y CONTROLES PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0577R2024 SSA and manufactured by CORPORINTER, S.A. DE C.V.. The device was registered on February 21, 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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