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F&P Visairo Non-Vented Hospital Under Nose Mask, Anti-Asphyxiation Valve Version - FDA Registration CMDR-2025-04221A

Access comprehensive regulatory information for F&P Visairo Non-Vented Hospital Under Nose 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-2025-04221A and manufactured by Fisher &paykel Healthcare Ltd. 15 Maurice Paykel Place East Tamaki, Aukland 2013, New Zealand Mfd By: Fisher & Paykel Healthcare S.A. de C.V. - Ave. Todos Los Santos 12831 Parque Industrial Pacifico 22643 Tijuana, Baja California, Mexico in New Zealand. The device was registered on April 01, 2025.

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.

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New Zealand
CMDR-2025-04221A
F&P Visairo Non-Vented Hospital Under Nose Mask, Anti-Asphyxiation Valve Version
Registered medical device in Philippines
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Device Information
Product Name
F&P Visairo Non-Vented Hospital Under Nose Mask, Anti-Asphyxiation Valve Version
Registration Number
CMDR-2025-04221A
Importer & Distribution
Importer/Distributor
Asia Actual Consultancy Inc.
Registration Dates
Issuance Date
April 01, 2025
Expiry Date
April 01, 2030