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UIBC - COFEPRIS Registration 1258R2020 SSA

Access comprehensive regulatory information for UIBC (UIBC) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 1258R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on September 15, 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
1258R2020 SSA
UIBC
COFEPRIS Analysis ID: 1258R2020 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA IN VITRO PARA DETERMINACIÓNCUANTITATIVADELACAPACIDADLATENTEDEFIJACIÓN DE HIERRO EN SUERO Y PLASMAHUMANOS EN LOS SISTEMAS ROCHE

English

IN VITRO TEST FOR QUANTITATIVE DETERMINATION OF LATENT IRON FIXATION CAPACITY IN HUMAN SERUM AND PLASMA IN ROCHE SYSTEMS

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)
PRUEBA PARA LA DETERMINACIÓNDE FIJACIÓN DE HIERRO
Trade Name (English)
TEST FOR THE DETERMINATION OF IRON FIXATION
Registration Information
Analysis ID
1258R2020 SSA
Registration Date
September 15, 2020
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DEC.V.