Mexico COFEPRIS registration 544R2019 SSA

DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN

EN: DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN
Mexico flagMexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.·Registered March 14, 2019
Product Use / Uso del Producto
Spanish

LOS MÉTODOS HCG Y LHCG ESTÁN DISEÑADOS PARA LA DETERMINACIÓN CUANTITATIVA DE LA GONADOTROPINA CORIÓNICA HUMANA INTACTA EN PLASMA Y SUERO HUMANOS

English

THE HCG AND LHCG METHODS ARE DESIGNED FOR THE QUANTITATIVE DETERMINATION OF INTACT HUMAN CHORIONIC GONADOTROPIN IN HUMAN PLASMA AND 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)
ENSAYO PARA LA DETERMINACIÓN DE GONADOTROPINA CORIÓNICA HUMANA
Trade Name (English)
ASSAY FOR THE DETERMINATION OF HUMAN CHORIONIC GONADOTROPIN
Registration information
Analysis ID
544R2019 SSA
Registration Date
March 14, 2019
Manufacturer / Fabricante
Name (English)
SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.
About this record

Access comprehensive regulatory information for DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN (DIMENSION® CLINICAL CHEMISTRY SYSTEM HUMAN CHORIONIC GONADOTROPIN) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 544R2019 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS, S. DE R.L. DE C.V.. The device was registered on March 14, 2019.

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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