AquaNASE® Nasal High Flow Cannula
Philippines·Armstrong Medical Ltd. Wattstown Business Park, Newbridge Road, Coleraine Northern, Ireland, BT52 1BS, UK·United Kingdom·Issued February 14, 2024 – February 14, 2029- Product Name
- AquaNASE® Nasal High Flow Cannula
- Registration Number
- CMDR-2022-00826
- Manufacturer
- Armstrong Medical Ltd. Wattstown Business Park, Newbridge Road, Coleraine Northern, Ireland, BT52 1BS, UK
- Country of Origin
- United Kingdom
- Importer/Distributor
- Healthsolutions Enterprises Inc.
- Issuance Date
- February 14, 2024
- Expiry Date
- February 14, 2029
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.