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HYDRAGEL 5 PROTEINURIE - COFEPRIS Registration 1290R2020 SSA

Access comprehensive regulatory information for HYDRAGEL 5 PROTEINURIE (HYDRAGEL 5 PROTEINURIA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1290R2020 SSA and manufactured by LABORATORIOS LICON, S.A.. The device was registered on September 25, 2020.

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
1290R2020 SSA
HYDRAGEL 5 PROTEINURIE
COFEPRIS Analysis ID: 1290R2020 SSA
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Product Use / Uso del Producto
Spanish

EL KIT HYDRAGEL 5 PROTEINURIE ESTรDISEร‘ADO PARA LA CLASIFICACIร“N DEPROTEINURIAS EN ORINAS NO CONCENTRADAS.

English

THE HYDRAGEL 5 PROTEINURIE KIT IS DESIGNED FOR THE CLASSIFICATION OF PROTEINURIAS IN UNCONCENTRATED URINE.

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)
KIT PARA LA CLASIFICACIร“N DEPROTEINURIAS EN ORINAS NOCONCENTRADAS
Trade Name (English)
KIT FOR THE CLASSIFICATION OF PROTEINURIAS IN UNCONCENTRATED URINE
Registration Information
Analysis ID
1290R2020 SSA
Registration Date
September 25, 2020
Manufacturer / Fabricante
Name (English)
LABORATORIOS LICON, S.A.