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ALINITY C ECSTASY REAGENT KIT - COFEPRIS Registration 2127R2021 SSA

Access comprehensive regulatory information for ALINITY C ECSTASY REAGENT KIT (ALINITY C ECSTASY REAGENT KIT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2127R2021 SSA and manufactured by ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on December 14, 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 II
2127R2021 SSA
ALINITY C ECSTASY REAGENT KIT
COFEPRIS Analysis ID: 2127R2021 SSA
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Product Use / Uso del Producto
Spanish

EL ENSAYO ALINITY C ECSTASY SE UTILIZAPARA LA DETERMINACIÓN CUALITATIVA YSEMICUANTITATIVA DE ÉXTASIS EN ORINAHUMANA EN EL ANALIZADOR ALINITY C.

English

THE ALINITY C ECSTASY ASSAY IS USED FOR THE QUALITATIVE AND SEMI-QUANTITATIVE DETERMINATION OF ECSTASY IN HUMAN URINE IN THE ALINITY C ANALYSER.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
III. AGENTES DE DIAGNÓSTICO
Product Type (English)
III. DIAGNOSTIC AGENTS
Trade Name (Spanish)
REACTIVO PARA LA DETERMINACIÓN DEÉXTASIS
Trade Name (English)
REAGENT FOR THE DETERMINATION OFECSTASY
Registration Information
Analysis ID
2127R2021 SSA
Registration Date
December 14, 2021
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DEMÉXICO, S.A. DE C.V.