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 86851. The device is manufactured by Teleflex Medical Sdn. Bhd. from Malaysia, 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.
Device Type
General Medical Device
Devices
Reinforced endotracheal tube, single-use
Type
Class IIa
Date Registered
Nov 26, 2024
Last Updated
Apr 12, 2024
Address
Lot No PT 2577 Jalan Perusahaan 4
Kamunting, Perak, Malaysia
Created Date
Apr 28, 2021
Name
TFX Group LtdRelationship Type
Address
Grosvenor House Horseshoe Crescent
Old Town Beaconsfield, England, United Kingdom
Postcode: HP9 1LJ
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