Tracheostomy tube, non-reinforced, non-customized, single-use - UK MHRA Medical Device Registration

Tracheostomy tube, non-reinforced, non-customized, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 89115. The device is manufactured by Teleflex Medical from Ireland, classified as General Medical Device. The authorized representative in the UK is TFX Group Ltd.

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Tracheostomy tube, non-reinforced, non-customized, single-use

MHRA Device ID: 89115•Ref: 89115

Device Type

General Medical Device

Devices

Tracheostomy tube, non-reinforced, non-customized, 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)

Tracheostomy tube, non-reinforced, non-customized, single-use - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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