RESMED MIRAGE FX FOR HER NASAL MASK SYSTEM - FDA Registration MDR-07322B

Access comprehensive regulatory information for RESMED MIRAGE FX FOR HER NASAL MASK SYSTEM in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number MDR-07322B and manufactured by Resmed Limited in Australia. The device was registered on November 05, 2019.

This page provides complete registration details including manufacturer information, importer/distributor details (Andaman Medical Philippines Corporation), 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.