Pure Global

URIC ACID2 - COFEPRIS Registration 0734R2022 SSA

Access comprehensive regulatory information for URIC ACID2 (URIC ACID2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0734R2022 SSA and manufactured by ABBOTTLABORATORIES DEMÉXICO, S.A. DE C.V.. The device was registered on August 08, 2022.

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.

Free Database
Powered by Pure Global AI
COFEPRIS Official Data
Clase I
0734R2022 SSA
URIC ACID2
COFEPRIS Analysis ID: 0734R2022 SSA
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Product Use / Uso del Producto
Spanish

ENSAYOPARALADETERMINACIÓNCUANTITATIVADEÁCIDOÚRICO

English

ASSAY for the quantitative determination of uric acid

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 LADETERMINACIÓN CUANTITATIVA DE ÁCIDO ÚRICO
Trade Name (English)
ASSAY FOR THE QUANTITATIVE DETERMINATION OF URIC ACID
Registration Information
Analysis ID
0734R2022 SSA
Registration Date
August 08, 2022
Manufacturer / Fabricante
Name (English)
ABBOTTLABORATORIES DE MÉXICO, S.A. DE C.V.