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ISE REAGENT PACK MINDRAY - COFEPRIS Registration 1954R2021 SSA

Access comprehensive regulatory information for ISE REAGENT PACK MINDRAY (ISE REAGENT PACK 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 1954R2021 SSA and manufactured by MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.. The device was registered on November 24, 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
1954R2021 SSA
ISE REAGENT PACK MINDRAY
COFEPRIS Analysis ID: 1954R2021 SSA
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Product Use / Uso del Producto
Spanish

EL KIT ISE REAGENT PACK ES PARA LOSANALIZADORES AUTOMATIZADOS DEQUÍMICAPERTENECIENTESALASERIEBSDEMINDRAY. EL OBJETIVO DE SU USO ES LADETECCIÓNDEELECTROLITOSENMUESTRASHUMANAS.

English

THE ISE REAGENT PACK KIT IS FOR AUTOMATED CHEMISTRY ANALYZERS BELONGING TO THE BSDEMINDRAY SERIES. THE PURPOSE OF ITS USE IS THE DETECTION OF ELECTROLYTES IN HUMAN SAMPLES.

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)
SOLUCIÓN DE DETECCIÓN DEELECTROLITOS
Trade Name (English)
ELECTROLYTE DETECTION SOLUTION
Registration Information
Analysis ID
1954R2021 SSA
Registration Date
November 24, 2021
Manufacturer / Fabricante
Name (English)
MINDRAY MEDICALMÉXICO, S. DE R.L. DEC.V.