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ALBP - COFEPRIS Registration 212R2020 SSA

Access comprehensive regulatory information for ALBP (ALBP) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 212R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on February 24, 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
212R2020 SSA
ALBP
COFEPRIS Analysis ID: 212R2020 SSA
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Product Use / Uso del Producto
Spanish

PARALADETERMINACIÓNCUANTITATIVADELAALBÚMINAENSUEROYPLASMAHUMANOSENLOS SISTEMAS ROCHE.

English

FOR THE QUANTITATIVE DETERMINATION OF ALBUMININ HUMAN 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 LA ALBÚMINA
Trade Name (English)
TEST FOR THE DETERMINATION OF ALBUMIN
Registration Information
Analysis ID
212R2020 SSA
Registration Date
February 24, 2020
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DEC.V.