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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 78907. The device is manufactured by Goodman Co., Ltd. Goodman Research Center from Japan, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) 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: 78907•Ref: 78907

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, basic

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

May 2, 2024

Manufacturer Information

Address

276-1 Idogane-cho, Seto,

Aichi, Japan

Created Date

Apr 30, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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