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ACP2 - COFEPRIS Registration 325R2020 SSA

Access comprehensive regulatory information for ACP2 (ACP2) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 325R2020 SSA and manufactured by PRODUCTOS ROCHE, S.A. DEC.V.. The device was registered on March 17, 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
325R2020 SSA
ACP2
COFEPRIS Analysis ID: 325R2020 SSA
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Product Use / Uso del Producto
Spanish

PRUEBA IN VITRO PARA LA DETERMINACIÓNCUANTITATIVA DE LA FOSFATASA ÁCIDA ENSUERO HUMANO EN LOS SISTEMAS ROCHE.

English

IN VITRO TEST FOR QUANTITATIVE DETERMINATION OF ACID PHOSPHATASE IN HUMAN SERUM 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 FOSFATASA ÁCIDA.
Trade Name (English)
TEST FOR THE DETERMINATION OF ACID PHOSPHATASE.
Registration Information
Analysis ID
325R2020 SSA
Registration Date
March 17, 2020
Manufacturer / Fabricante
Name (English)
PRODUCTOS ROCHE, S.A. DEC.V.