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EQUIPOS FORMULA® - COFEPRIS Registration 2379E2018 SSA

Access comprehensive regulatory information for EQUIPOS FORMULA® (FORMULA TEAMS®) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2379E2018 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on October 16, 2018.

This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), 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 II
2379E2018 SSA
EQUIPOS FORMULA®
COFEPRIS Analysis ID: 2379E2018 SSA
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Product Use / Uso del Producto
Spanish

EQUIPOS DE HEMODIÁLISIS Y HEMOFILTRACIÓN PARA TRATAMIENTO DE DIÁLISIS CON ACETATO O BICARBONATO EN PACIENTES CON INSUFICIENCIA RENAL CRÓNICA. PUEDE UTILIZARSE EN HOSPITAL O DOMICILIO.

English

HAEMODIALYSIS AND HAEMOFILTRATION EQUIPMENT FOR DIALYSIS TREATMENT WITH ACETATE OR BICARBONATE IN PATIENTS WITH CHRONIC RENAL FAILURE. IT CAN BE USED IN HOSPITAL OR AT HOME.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
EQUIPOS Y ACCESORIOS PARA HEMODIÁLISIS
Trade Name (English)
EQUIPMENT AND ACCESSORIES FOR HEMODIALYSIS
Registration Information
Analysis ID
2379E2018 SSA
Registration Date
October 16, 2018
Manufacturer / Fabricante
Name (English)
KENDALL DE MÉXICO, S.A. DE C.V.