Exhaled-gas oesophageal intubation detector, paediatric - UK MHRA Medical Device Registration

Exhaled-gas oesophageal intubation detector, paediatric is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 86780. The device is manufactured by Westmed Inc. from United States, classified as General Medical Device. The authorized representative in the UK is MT Promedt Consulting Ltd.

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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Exhaled-gas oesophageal intubation detector, paediatric

MHRA Device ID: 86780•Ref: 86780

Device Type

General Medical Device

Devices

Exhaled-gas oesophageal intubation detector, paediatric

Type

Class IIa

Date Registered

Jun 29, 2021

Last Updated

Oct 13, 2022

Manufacturer Information

Name

Westmed Inc.

Address

5580 S. Nogales Highway

Tucson, Arizona, United States

Created Date

Jun 29, 2021

Authorized Representative

Name

MT Promedt Consulting Ltd

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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Exhaled-gas oesophageal intubation detector, paediatric - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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