Nonconductive Respiratory Therapy Filter, Bacterial/ Viral Retentive - Airlife™ - FDA Registration CMDR-2025-04797

Access comprehensive regulatory information for Nonconductive Respiratory Therapy Filter, Bacterial/ Viral Retentive - Airlife™ in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2025-04797 and manufactured by AirLife - 2710 Northridge Dr. NW, Suite A, Grand Rapids, MI 49544, USA Mfd. By: Productos Urólogos de México S.A. de C.V. - Cerrada Via de la Produccion No. 85, Parque Industrial Mexicali III Baja California, CP 21397, Mexico in United States. The device was registered on June 05, 2025.

This page provides complete registration details including manufacturer information, importer/distributor details (Lifelink, Inc.), and regulatory compliance data from the official Philippines FDA medical device database. Pure Global AI offers free access to Philippines' complete medical device registry, helping global MedTech companies navigate FDA regulations efficiently.