Tracheostomy tube, reinforced, non-customized, single-use - UK MHRA Medical Device Registration
Tracheostomy tube, reinforced, non-customized, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 201319. 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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Device Type
General Medical Device
Devices
Tracheostomy tube, reinforced, non-customized, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Apr 12, 2024
Name
Teleflex MedicalAddress
IDA Business and Technology Park Dublin Road
Athlone, Co. Westmeath, Ireland
Created Date
Apr 19, 2021
Name
TFX Group LtdRelationship Type
Address
Grosvenor House Horseshoe Crescent
Old Town Beaconsfield, England, United Kingdom
Postcode: HP9 1LJ
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