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

Peripheral angioplasty balloon catheter, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 160525. The device is manufactured by Cordis Cashel from Ireland, classified as General Medical Device. The authorized representative in the UK is Cordis Medical UK Limited.

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Peripheral angioplasty balloon catheter, basic

MHRA Device ID: 160525•Ref: 160525

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 10, 2023

Manufacturer Information

Name

Cordis Cashel

Address

Cahir Road

Cashel, Co. Tipperary, Ireland

Created Date

Nov 14, 2022

Authorized Representative

Name

Cordis Medical UK Limited

Relationship Type

UK Responsible Person

Address

Suite 402, Chadwick House Birchwood Park

Warrington, England, United Kingdom

Postcode: WA3 6AE

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

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Peripheral angioplasty balloon catheter, basic