Coronary angioplasty balloon catheter, basic - UK MHRA Medical Device Registration

Coronary angioplasty balloon catheter, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 156408. The device is manufactured by Shunmei 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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Coronary angioplasty balloon catheter, basic

MHRA Device ID: 156408•Ref: 156408

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, basic

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Nov 18, 2023

Manufacturer Information

Name

Shunmei Medical Co., Ltd.

Address

R401 of Building B, No.8 of 1st Jinglong Road, Baolong Industrial Zone, Longgang District, Shenzhen

Guangdong Province, China

Created Date

Sep 20, 2022

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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Coronary angioplasty balloon catheter, basic - UK MHRA Medical Device Registration

Device Type

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Date Registered

Last Updated

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Address

Created Date

Name

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Address

DJ Fang

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