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ALINITY C AMMONIA - COFEPRIS Registration 50R2019 SSA

Access comprehensive regulatory information for ALINITY C AMMONIA (ALINITY C AMMONIA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 50R2019 SSA and manufactured by ABBOTT LABORATORIES DE MEXICO SA DE CV. The device was registered on January 23, 2019.

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
50R2019 SSA
ALINITY C AMMONIA
COFEPRIS Analysis ID: 50R2019 SSA
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Product Use / Uso del Producto
Spanish

ENSAYO PARA LA DETERMINACION ENZIMATICA DE AMONIO

English

TEST FOR THE ENZYMATIC DETERMINATION OF AMMONIUM

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)
ENSAYO PARA LA DETERMINACION ENZIMATICA DE AMONIO
Trade Name (English)
TEST FOR THE ENZYMATIC DETERMINATION OF AMMONIUM
Registration Information
Analysis ID
50R2019 SSA
Registration Date
January 23, 2019
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MEXICO SA DE CV