INNOSPIRE GO - COFEPRIS Registration 23E2019 SSA
Access comprehensive regulatory information for INNOSPIRE GO (INNOSPIRE GO) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 23E2019 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on January 15, 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.
INNOSPIRE GO ES UN NEBULIZADOR DE MALLA PARA APLICACIONES GENERALES QUE ESTÁ DESTINADO A SER UTILIZADO PARA NEBULIZAR MEDICAMENTOS LÍQUIDOS POR INHALACIÓN COMÚNMENTE PRESCRITOS PARA LA ENFERMEDAD RESPIRATORIA. ESTÁ PREVISTO PARA SER USADO POR UN SOLO PACI
INNOSPIRE GO IS A MESH NEBULIZER FOR GENERAL APPLICATIONS THAT IS INTENDED TO BE USED TO NEBULIZE INHALATION LIQUID MEDICATIONS COMMONLY PRESCRIBED FOR RESPIRATORY DISEASE. IT IS INTENDED TO BE USED BY A SINGLE PACI