Mexico COFEPRIS registration 2431R2018 SSA

ATELLICA TM IM FOLATO

EN: ATELLICA TM IN FOLATO

Mexico·Clase I·III. DIAGNOSTIC AGENTS·SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV·Registered October 23, 2018

Product Use / Uso del Producto

Spanish

ENSAYO PARA LA DETERMINACION DE FOLATO

English

FOLATE ASSAY

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 DETERMINACION DE FOLATO
Trade Name (English): FOLATE ASSAY

Registration information

Analysis ID: 2431R2018 SSA
Registration Date: October 23, 2018

Manufacturer / Fabricante

Name (Spanish): SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV
Name (English): SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR

About this record

Access comprehensive regulatory information for ATELLICA TM IM FOLATO (ATELLICA TM IN FOLATO) in the Mexico medical device market through Pure Global AI's free database. This Clase I medical device is registered under COFEPRIS analysis ID 2431R2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on October 23, 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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