Reinforced endotracheal tube, single-use - UK MHRA Medical Device Registration

Reinforced endotracheal tube, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189956. The device is manufactured by Teleflex Medical from Ireland, classified as General Medical Device. The authorized representative in the UK is TFX Group 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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Reinforced endotracheal tube, single-use

MHRA Device ID: 189956•Ref: 189956

Device Type

General Medical Device

Devices

Reinforced endotracheal tube, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 12, 2024

Manufacturer Information

Name

Teleflex Medical

Address

IDA Business and Technology Park Dublin Road

Athlone, Co. Westmeath, Ireland

Created Date

Apr 19, 2021

Authorized Representative

Name

TFX Group Ltd

Relationship Type

UK Responsible Person

Address

Grosvenor House Horseshoe Crescent

Old Town Beaconsfield, England, United Kingdom

Postcode: HP9 1LJ

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Other Products from Teleflex Medical (10)

Other Products from Same Authorized Representative (10)

Reinforced endotracheal tube, 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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