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 91453. 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.

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Inspiratory line humidification chamber, single-use

MHRA Device ID: 91453•Ref: 91453

Device Type

General Medical Device

Devices

Inspiratory line humidification chamber, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Mar 26, 2024

Manufacturer Information

Name

Fisher & Paykel Healthcare Ltd

Address

15 Maurice Paykel Place, East Tamaki

Auckland, Auckland, New Zealand

Created Date

Mar 1, 2021

Authorized Representative

Name

Fisher & Paykel Healthcare Limited

Relationship Type

UK Responsible Person

Address

16 Cordwallis Park

Maidenhead, England, United Kingdom

Postcode: SL67BU

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Other Products from Fisher & Paykel Healthcare Ltd (10)

Other Products from Same Authorized Representative (10)

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

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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