Airlife™ Prefilled Humidifier with Sterile Water for Inhalation 500ml USP with Adapter - FDA Registration MDR-01221

Access comprehensive regulatory information for Airlife™ Prefilled Humidifier with Sterile Water for Inhalation 500ml USP with Adapter in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-01221 and manufactured by Vital Signs,Inc.- Princeton South Corporate Center, 100 Charles Ewing Blvd., Suite 160, Ewing New Jersey, USA Mfd by: Productos Urologos de Mexico S.A. De C.V- Cerrada via de la Produccion No. 85 Parque Industrial Mexicali III Baja California, Mexico in Mexico. The device was registered on August 02, 2024.

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.