Mexico COFEPRIS registration 41R2018 SSA

NEO-NATAL T4 ELISA

EN: NEONATAL T4 ELISA
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·DIAGMEX, S.A. DE C.V.·Registered January 03, 2018
Product Use / Uso del Producto
Spanish

LA PRUEBA NEO-NATAL T4 ELISA ES UN SISTEMA PARA LA DETERMINACIÓN CUANTITATIVA DE LA CONCENTRACIÓN TOTAL DE TIROXINA EN SANGRE HUMANA (RECIÉN NACIDOS) MEDIANTE UN INMUNOENSAYO ENZIMÁTICO.

English

THE NEONATAL T4 ELISA TEST IS A SYSTEM FOR THE QUANTITATIVE DETERMINATION OF THE TOTAL CONCENTRATION OF THYROXINE IN HUMAN BLOOD (NEWBORNS) BY AN ENZYME IMMUNOASSAY.

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)
REACTIVOS PARA LA DETERMINACIÓN DE TIROXINA
Trade Name (English)
REAGENTS FOR THE DETERMINATION OF THYROXINE
Registration information
Analysis ID
41R2018 SSA
Registration Date
January 03, 2018
Manufacturer / Fabricante
Name (Spanish)
DIAGMEX, S.A. DE C.V.
Name (English)
DIAGMEX, S.A. DE C.V.
About this record

Access comprehensive regulatory information for NEO-NATAL T4 ELISA (NEONATAL T4 ELISA) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 41R2018 SSA and manufactured by DIAGMEX, S.A. DE C.V.. The device was registered on January 03, 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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