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 70500. The device is manufactured by Haiyan Kangyuan Medical Instrument Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is MedPath Limited.
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
Dec 30, 2023
Address
Songpodong Rd., Shendang Town
Haiyan, Zhejiang , China
Created Date
Mar 25, 2021
Name
MedPath LimitedRelationship Type
Address
27 Old Gloucester Street
London, England, United Kingdom
Postcode: WC1N 3AX
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