F & P Nivairo+™Non-Vented Hospital Full Face Mask, Anti-Asphyxiation Valve Version - FDA Registration CMDR-2022-00609A

Access comprehensive regulatory information for F & P Nivairo+™Non-Vented Hospital Full Face Mask, Anti-Asphyxiation Valve Version in the Philippines medical device market through Pure Global AI's free database. This device is registered under FDA registration number CMDR-2022-00609A and manufactured by Fisher & Paykel Healthcare Ltd. - Auckland, New Zealand Mfd By: Fisher & Paykel Healthcare S.A. de C.V - Tijuana Baja, California, Mexico in New Zealand. The device was registered on July 15, 2022.

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.