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ENSAYO PARA LA DETERMINACIÓN DE ÁCIDO ÚRICO - COFEPRIS Registration 0635R2022 SSA

Access comprehensive regulatory information for ENSAYO PARA LA DETERMINACIÓN DE ÁCIDO ÚRICO (ENSAYO PARA LA DETERMINACIÓN DE ÁCIDO ÚRICO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 0635R2022 SSA and manufactured by ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.. The device was registered on July 20, 2023.

This page provides complete registration details including product type (III. Agentes de diagnóstico), 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
0635R2022 SSA
ENSAYO PARA LA DETERMINACIÓN DE ÁCIDO ÚRICO
COFEPRIS Analysis ID: 0635R2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase I
Product Type (Spanish)
III. Agentes de diagnóstico
Product Type (English)
III. Agentes de diagnóstico
Trade Name (Spanish)
URIC ACID (ÁCIDO ÚRICO)
Trade Name (English)
URIC ACID (ÁCIDO ÚRICO)
Registration Information
Analysis ID
0635R2022 SSA
Registration Date
July 20, 2023
Manufacturer / Fabricante
Name (English)
ABBOTT LABORATORIES DE MÉXICO, S.A. DE C.V.