AquaNASE® Nasal High Flow Cannula - FDA Registration CMDR-2022-00826

Access comprehensive regulatory information for AquaNASE® Nasal High Flow Cannula in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00826 and manufactured by Armstrong Medical Ltd. Wattstown Business Park, Newbridge Road, Coleraine Northern, Ireland, BT52 1BS, UK in United Kingdom. The device was registered on February 14, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Healthsolutions Enterprises 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.