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ALINITY C TRANSFERRIN - COFEPRIS Registration 2223R2021 SSA

Access comprehensive regulatory information for ALINITY C TRANSFERRIN (ALINITY C TRANSFERRIN) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2223R2021 SSA and manufactured by ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on December 27, 2021.

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
2223R2021 SSA
ALINITY C TRANSFERRIN
COFEPRIS Analysis ID: 2223R2021 SSA
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Product Use / Uso del Producto
Spanish

ELENSAYOTRANSFERRINASEUTILIZAPARALA DETERMINACIÓN CUANTITATIVA DETRANSFERRINA EN SUERO O PLASMAHUMANOSENELALINITYCSYSTEM. AGENTEDEDIAGNÓSTICOPARAUSOINVITRO.PARAUSOEXCLUSIVOENLABORATORIOSCLÍNICOSY DE GABINETE.

English

THE TRANSFERRIN ASSAY IS USED FOR THE QUANTITATIVE DETERMINATION OF TRANSFERRIN IN HUMAN SERUM OR PLASMA IN THE LINITYCSYSTEM. DIAGNOSTICAGENTFORUSEINVITRO. FOR EXCLUSIVE USE IN CLINICAL AND CABINET LABORATORIES.

Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
ENSAYO PARA LA DETERMINACIÓNCUANTITATIVA DE TRANSFERRINA
Trade Name (English)
TEST FOR THE QUANTITATIVE DETERMINATION OF TRANSFERRIN
Registration Information
Analysis ID
2223R2021 SSA
Registration Date
December 27, 2021
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.