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.

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Reinforced endotracheal tube, single-use

MHRA Device ID: 70500•Ref: 70500

Device Type

General Medical Device

Devices

Reinforced endotracheal tube, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 30, 2023

Manufacturer Information

Name

Haiyan Kangyuan Medical Instrument Co., Ltd.

Address

Songpodong Rd., Shendang Town

Haiyan, Zhejiang , China

Created Date

Mar 25, 2021

Authorized Representative

Name

MedPath Limited

Relationship Type

UK Responsible Person

Address

27 Old Gloucester Street

London, England, United Kingdom

Postcode: WC1N 3AX

DJ Fang

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Other Products from Haiyan Kangyuan Medical Instrument Co., Ltd. (10)

Other Products from Same Authorized Representative (10)

Reinforced endotracheal tube, single-use - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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