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

Coronary angioplasty balloon catheter, perfusing is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 133257. The device is manufactured by Shenzhen Antmed Co., Ltd. from China, classified as General Medical Device. The authorized representative in the UK is Medimap Ltd.

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, perfusing

MHRA Device ID: 133257•Ref: 133257

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, perfusing

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Mar 23, 2024

Manufacturer Information

Name

Shenzhen Antmed Co., Ltd.

Address

18 Jinhui Ave

Shenzhen, Pingshan New District, China

Created Date

Jan 20, 2022

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Coronary angioplasty balloon catheter, perfusing - 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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