F&P Optiflow + Duet Nasal Cannula - FDA Registration CMDR-2024-02863

Access comprehensive regulatory information for F&P Optiflow + Duet Nasal Cannula in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2024-02863 and manufactured by Fisher & Paykel Healthcare Ltd. 15 Maurice Paykel Place, East Tamaki, Auckland 2013, New Zealand in New Zealand. The device was registered on June 13, 2024.

This page provides complete registration details including manufacturer information, importer/distributor details (Asia Actual Consultancy 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.