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ALINITY C ACTIVATED AMINOTRANFERASA - COFEPRIS Registration 23R2018 SSA

Access comprehensive regulatory information for ALINITY C ACTIVATED AMINOTRANFERASA (ALINITY C ACTIVATED AMINOTRANFERASA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 23R2018 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
23R2018 SSA
ALINITY C ACTIVATED AMINOTRANFERASA
COFEPRIS Analysis ID: 23R2018 SSA
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Product Use / Uso del Producto
Spanish

SE UTILIZA PARA LA DETERMINACION CUANTITATIVA DE ALANINA AMINOTRANSFERASA EN SUERO O PLASMA HUMANOS EN EL ANALIZADOR ALINITY C

English

IT IS USED FOR THE QUANTITATIVE DETERMINATION OF ALANINE AMINOTRANSFERASE IN HUMAN SERUM OR PLASMA IN THE ALINITY C ANALYZER

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 ALANINA AMINOTRANSFERASA
Trade Name (English)
REAGENT FOR THE DETERMINATION OF ALANINE AMINOTRANSFERASE
Registration Information
Analysis ID
23R2018 SSA
Registration Date
January 03, 2018
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MEXICO SA DE CV