Professional high-flow respiratory unit, humidifying, manual - UK MHRA Medical Device Registration
Professional high-flow respiratory unit, humidifying, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 202684. The device is manufactured by Fisher & Paykel Healthcare Ltd from New Zealand, classified as General Medical Device. The authorized representative in the UK is Fisher & Paykel Healthcare Limited.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
Device Type
General Medical Device
Devices
Professional high-flow respiratory unit, humidifying, manual
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Mar 26, 2024
Address
15 Maurice Paykel Place, East Tamaki
Auckland, Auckland, New Zealand
Created Date
Mar 1, 2021
Relationship Type
Address
16 Cordwallis Park
Maidenhead, England, United Kingdom
Postcode: SL67BU
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