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 78914. The device is manufactured by Creganna Medical from Ireland, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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Coronary angioplasty balloon catheter, basic

MHRA Device ID: 78914•Ref: 78914

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Oct 4, 2024

Last Updated

May 1, 2024

Manufacturer Information

Name

Creganna Medical

Address

Parkmore West

Galway, Ireland

Created Date

Apr 30, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

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

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