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ALINITY I CORTISOL - COFEPRIS Registration 24R2018 SSA

Access comprehensive regulatory information for ALINITY I CORTISOL (ALINITY I CORTISOL) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 24R2018 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on January 03, 2018.

This page provides complete registration details including product type (III. DIAGNOSTIC AGENTS), 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
24R2018 SSA
ALINITY I CORTISOL
COFEPRIS Analysis ID: 24R2018 SSA
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Product Use / Uso del Producto
Spanish

ES UN INMUNOANALISIS DE MICROPARTICULAS (CMIA) UTILIZADO PARA LA DETERMINACION CUANTITATIVA DE CORTISOL EN SUERO, PLASMA U ORINA HUMANOS

English

IT IS A MICROPARTICLE IMMUNOASSAY (CMIA) USED FOR THE QUANTITATIVE DETERMINATION OF CORTISOL IN HUMAN SERUM, PLASMA OR URINE

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNร“STICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACION DE CORTISOL
Trade Name (English)
REAGENT FOR THE DETERMINATION OF CORTISOL
Registration Information
Analysis ID
24R2018 SSA
Registration Date
January 03, 2018
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MEXICO SA DE CV