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IMMUNOLOGY KIT FERRITIN MINDRAY - COFEPRIS Registration 1371R2018 SSA

Access comprehensive regulatory information for IMMUNOLOGY KIT FERRITIN MINDRAY (IMMUNOLOGY KIT FERRITIN 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 1371R2018 SSA and manufactured by MINDRAY MEDICAL MÉXICO, S. DE R.L. DE C.V.. The device was registered on June 05, 2018.

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
1371R2018 SSA
IMMUNOLOGY KIT FERRITIN MINDRAY
COFEPRIS Analysis ID: 1371R2018 SSA
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Product Use / Uso del Producto
Spanish

KIT DE REACTIVOS PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA (FERR) A TRAVÉS DE UN INMUNOENSAYO DE QUIMIOLUMINISCENCIA (CLIA) EN PLASMA O SUERO HUMANOS.

English

KIT OF REAGENTS FOR THE QUANTITATIVE DETERMINATION OF FERRITIN (FERR) THROUGH A CHEMILUMINESCENCE IMMUNOASSAY (CLIA) IN HUMAN PLASMA OR SERUM.

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)
KIT PARA LA DETERMINACIÓN CUANTITATIVA DE FERRITINA
Trade Name (English)
KIT FOR THE QUANTITATIVE DETERMINATION OF FERRITIN
Registration Information
Analysis ID
1371R2018 SSA
Registration Date
June 05, 2018
Manufacturer / Fabricante
Name (English)
MINDRAY MEDICAL MEXICO, S. DE R.L. DE C.V.