Mexico COFEPRIS registration 26E2019 SSA

PHILIPS HOME NEBULIZER

EN: PHILIPS HOME NEBULIZER
Mexico flagMexico·Clase II·I. MEDICAL EQUIPMENT·PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.·Registered January 16, 2019
Product Use / Uso del Producto
Spanish

PHILIPS HOME NEBULIZER ES UN SISTEMA ELÉCTRICO DE NEBULIZADOR CON COMPRESOR DE AIRE PREVISTO PARA PROVEER UNA FUENTE DE AIRE COMPRIMIDO CON FINES MÉDICOS PARA USAR EN LA ATENCIÓN DE SALUD EN CASA. SE USA CON UN NEBULIZADOR NEUMÁTICO A FIN DE PRODUCIR PART

English

PHILIPS HOME NEBULIZER IS AN ELECTRICAL NEBULIZER SYSTEM WITH AIR COMPRESSOR INTENDED TO PROVIDE A SOURCE OF COMPRESSED AIR FOR MEDICAL PURPOSES FOR USE IN HOME HEALTH CARE. USED WITH A PNEUMATIC NEBULIZER TO PRODUCE PART

Device classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
I. EQUIPO MÉDICO
Product Type (English)
I. MEDICAL EQUIPMENT
Trade Name (Spanish)
SISTEMA NEBULIZADOR CON COMPRESOR
Trade Name (English)
NEBULIZER SYSTEM WITH COMPRESSOR
Registration information
Analysis ID
26E2019 SSA
Registration Date
January 16, 2019
Manufacturer / Fabricante
Name (English)
PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.
About this record

Access comprehensive regulatory information for PHILIPS HOME NEBULIZER (PHILIPS HOME NEBULIZER) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 26E2019 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on January 16, 2019.

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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