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ATELLICA TM IM FOLATO - COFEPRIS Registration 2431R2018 SSA

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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COFEPRIS Official Data
Clase I
2431R2018 SSA
ATELLICA TM IM FOLATO
COFEPRIS Analysis ID: 2431R2018 SSA
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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 DIAGNร“STICO
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 (English)
SIEMENS HEALTHCARE DIAGNOSTICS S OF CV LR