Neonatal/adult intensive-care ventilator - UK MHRA Medical Device Registration

Neonatal/adult intensive-care ventilator is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 95101. The device is manufactured by Datex-Ohmeda Inc from United States, classified as General Medical Device. The authorized representative in the UK is GE Medical Systems 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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Neonatal/adult intensive-care ventilator

MHRA Device ID: 95101•Ref: 95101

Device Type

General Medical Device

Devices

Neonatal/adult intensive-care ventilator

Type

Class IIb

Date Registered

Aug 16, 2021

Last Updated

Oct 28, 2022

Manufacturer Information

Name

Datex-Ohmeda Inc

Address

3030 Ohmeda Drive

Madison, United States

Created Date

Aug 16, 2021

Authorized Representative

Name

GE Medical Systems Limited

Relationship Type

UK Responsible Person

Address

Pollards Wood Nightingales Lane Buckinghamshire

Chalfont St Giles, England, United Kingdom

Postcode: HP8 4SP

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Neonatal/adult intensive-care ventilator - 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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