General-purpose intensive-care ventilator - UK MHRA Medical Device Registration

General-purpose intensive-care ventilator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 100865. The device is manufactured by AIR LIQUIDE MEDICAL SYSTEMS S.A. from France, classified as General Medical Device. The authorized representative in the UK is Air Liquide 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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General-purpose intensive-care ventilator

MHRA Device ID: 100865•Ref: 100865

Device Type

General Medical Device

Devices

General-purpose intensive-care ventilator

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Aug 8, 2024

Manufacturer Information

Name

AIR LIQUIDE MEDICAL SYSTEMS S.A.

Address

Parc de Haute Technologie 6, rue Georges Besse

ANTONY, France

Created Date

Aug 30, 2021

Authorized Representative

Name

Air Liquide Healthcare Limited

Relationship Type

UK Responsible Person

Address

Station Road Coleshill Birmingham

Birmingham, West Midlands, England, United Kingdom

Postcode: B46 1JY

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General-purpose intensive-care ventilator - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Created Date

Name

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Address

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