Sleep-disordered breathing nasopharyngeal stent, reusable - UK MHRA Medical Device Registration

Sleep-disordered breathing nasopharyngeal stent, reusable is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195830. The device is manufactured by Henan Geesion Medical Device 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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Sleep-disordered breathing nasopharyngeal stent, reusable

MHRA Device ID: 195830•Ref: 195830

Device Type

General Medical Device

Devices

Sleep-disordered breathing nasopharyngeal stent, reusable

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jun 29, 2024

Manufacturer Information

Name

Henan Geesion Medical Device Co., Ltd

Address

No.2009-046,2nd Floor, Science and Technology Building, No.73-10 Wenhua Road, Dongfeng Road, Jinshui District

Zhengzhou, China

Created Date

Jun 25, 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 Henan Geesion Medical Device Co., Ltd (1)

CPAP/BPAP chin strap, reusable

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Sleep-disordered breathing nasopharyngeal stent, reusable - UK MHRA Medical Device Registration

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