Endotracheal tube guide, single-use - UK MHRA Medical Device Registration
Endotracheal tube guide, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 119557. The device is manufactured by Vygon from France, classified as General Medical Device. The authorized representative in the UK is Vygon (UK) 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
Endotracheal tube guide, single-use
Type
Class I
Date Registered
Nov 26, 2024
Last Updated
Oct 9, 2024
Name
Vygon (UK) LtdRelationship Type
Address
The Pierre Simonet Building, V Park, Gateway North Latham Road
Swindon, Wiltshire, United Kingdom
Postcode: SN25 4DL
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