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 195547. The device is manufactured by Jiangsu Hitec Medical Co., Ltd from China, classified as General Medical Device. The authorized representative in the UK is SUNGO Certification Company 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: 195547•Ref: 195547

Device Type

General Medical Device

Devices

Reinforced endotracheal tube, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 1, 2024

Manufacturer Information

Name

Jiangsu Hitec Medical Co., Ltd

Address

North Jiang Xin Road Jianghai Linkage Development Zone, Tongzhou Bay, Nantong City

Jiangsu Province, China

Created Date

May 29, 2024

Authorized Representative

Name

SUNGO Certification Company Limited

Relationship Type

UK Responsible Person

Address

3rd Floor, 70 Gracechurch Street

London, England, United Kingdom

Postcode: EC3V 0HR

DJ Fang

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Other Products from Jiangsu Hitec Medical 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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