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Inspiratory line humidification chamber, single-use - UK MHRA Medical Device Registration

Inspiratory line humidification chamber, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 205854. The device is manufactured by Fisher & Paykel Healthcare Ltd from New Zealand, classified as General Medical Device.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, 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.

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General Medical Device
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Inspiratory line humidification chamber, single-use
MHRA Device ID: 205854

Device Type

General Medical Device

Type

Class IIa

Status

DREGIY

Date Registered

Nov 27, 2024

Manufacturer Information

Address

15 Maurice Paykel Place, East Tamaki

Auckland, Auckland, New Zealand

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