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URIDIAG. - COFEPRIS Registration 2041R2019 SSA

Access comprehensive regulatory information for URIDIAG. (URIDIAG.) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2041R2019 SSA and manufactured by QUIMIBIOL, S.A. DE C.V.. The device was registered on October 25, 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
2041R2019 SSA
URIDIAG.
COFEPRIS Analysis ID: 2041R2019 SSA
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Product Use / Uso del Producto
Spanish

TIRAS REACTIVAS DE URIANÁLISIS. AGENTE DE DIAGNÓSTICO PARA USO IN VITRO. PARA USO EXCLUSIVO EN LABORATORIOS CLÍNICOS O DE GABINETE.

English

URINALYSIS TEST STRIPS. DIAGNOSTIC AGENT FOR IN VITRO USE. FOR USE IN CLINICAL OR CABINET LABORATORIES ONLY.

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)
TIRAS REACTIVAS.
Trade Name (English)
TEST STRIPS.
Registration Information
Analysis ID
2041R2019 SSA
Registration Date
October 25, 2019
Manufacturer / Fabricante
Name (English)
QUIMIBIOL, S.A. DE C.V.