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 159191. The device is manufactured by Cordis Corporation from United States, 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: 159191•Ref: 159191

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Nov 11, 2023

Manufacturer Information

Name

Cordis Corporation

Address

14201 North West 60th Avenue

Miami Lakes, Florida, United States

Created Date

Oct 28, 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