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AMMONIA - COFEPRIS Registration 88R2019 SSA

Access comprehensive regulatory information for AMMONIA (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 88R2019 SSA and manufactured by REPRESENTACIONES LABIN MEXICO SA DE CV. The device was registered on January 28, 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
88R2019 SSA
AMMONIA
COFEPRIS Analysis ID: 88R2019 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACION DE AMONIACO

English

REAGENT FOR THE DETERMINATION OF AMMONIA

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 AMONIACO
Trade Name (English)
REAGENT FOR THE DETERMINATION OF AMMONIA
Registration Information
Analysis ID
88R2019 SSA
Registration Date
January 28, 2019
Manufacturer / Fabricante
Name (English)
REPRESENTATIONS LABIN MEXICO SA DE CV