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 87223. The device is manufactured by Venner Medical (Singapore) Pte Ltd. from Singapore, classified as General Medical Device. The authorized representative in the UK is Advena 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
Tracheostomy tube, non-reinforced, non-customized, single-use
Type
Class IIa
Date Registered
Sep 24, 2024
Last Updated
Jun 7, 2024
Address
35 Joo Koon Circle
Singapore, Singapore
Created Date
Jul 2, 2021
Name
Advena LtdRelationship Type
Address
Pure Offices Plato Close
Warwick, England, United Kingdom
Postcode: CV34 6WE
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