Humidified oxygen administration set - UK MHRA Medical Device Registration
Humidified oxygen administration set is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 211806. The device is manufactured by Fisher & Paykel Healthcare Ltd from New Zealand, classified as General Medical Device.
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Device Type
General Medical Device
Type
Class IIa
Status
Date Registered
Feb 27, 2025
Address
15 Maurice Paykel Place, East Tamaki
Auckland, Auckland, New Zealand
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