PHILIPS HOME NEBULIZER - COFEPRIS Registration 26E2019 SSA
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.
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
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