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REAGENTKITFORPREALBUMINKIT(PA) MINDRAY - COFEPRIS Registration 2039R2021 SSA

Access comprehensive regulatory information for REAGENTKITFORPREALBUMINKIT(PA) MINDRAY (REAGENTKITFORPREALBUMINKIT(PA) MINDRAY) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2039R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on February 12, 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
2039R2021 SSA
REAGENTKITFORPREALBUMINKIT(PA) MINDRAY
COFEPRIS Analysis ID: 2039R2021 SSA
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Product Use / Uso del Producto
Spanish

PRUEBAS PARA DETERMINACIÓNCUANTITATIVADELACONCENTRACIÓNDEPAMEN SUERO EN SISTEMAS FOTOMÉTRICOS

English

TESTS FOR QUANTITATIVE DETERMINATION OF SERUM CONCENTRATION IN PHOTOMETRIC 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)
REACTIVO PARA LA DETERMINACIÓN DEPREALBÚMINA MEDIANTE MÉTODO DETURBIDIMÉTRICO
Trade Name (English)
REAGENT FOR THE DETERMINATION OF PREALBUMIN BY METHOD DETURBIDIMÉTRICO
Registration Information
Analysis ID
2039R2021 SSA
Registration Date
February 12, 2021
Manufacturer / Fabricante
Name (English)
MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.