Urethral dilator, single-use - UK MHRA Medical Device Registration

Urethral dilator, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 186180. The device is manufactured by Well Lead 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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Urethral dilator, single-use

MHRA Device ID: 186180•Ref: 186180

Device Type

General Medical Device

Devices

Urethral dilator, single-use

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jun 20, 2024

Manufacturer Information

Name

Well Lead Medical Co., Ltd.

Address

C-4 Jinhu Industrial Estate, Hualong, Panyu

Guangzhou, China

Created Date

Jul 21, 2021

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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Urethral dilator, single-use - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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