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UIBC - COFEPRIS Registration 713R2021 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 713R2021 SSA and manufactured by HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.. The device was registered on April 23, 2021.

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
713R2021 SSA
UIBC
COFEPRIS Analysis ID: 713R2021 SSA
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Product Use / Uso del Producto
Spanish

REACTIVO PARA LA DETERMINACIÓNCUANTITATIVA IN VITRO DE LA CAPACIDADINSATURADA DE LA UNIÓN DE HIERRO ENSUERO Y PLASMA. ENSAYO FOTOMÉTRICOUTILIZANDO CROMÓGENO DE FERROZINA.

English

REAGENT FOR THE QUANTITATIVE DETERMINATION IN VITRO OF THE UNSATURATED CAPACITY OF THE UNION OF SERUM IRON AND PLASMA. PHOTOMETRIC TEST USING FERROZINE CHROMOGEN.

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)
REACTIVODEDIAGNÓSTICOINVITROPARAHIERRO
Trade Name (English)
REACTIVODEDIAGNÓSTICOINVITROPARAHIERRO
Registration Information
Analysis ID
713R2021 SSA
Registration Date
April 23, 2021
Manufacturer / Fabricante
Name (English)
HRD HIGHRESOLUTION DIAGNOSTICS, S.A. DEC.V.