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 160520. The device is manufactured by Clearstream Technologies Ltd. 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: 160520•Ref: 160520

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Jul 8, 2024

Last Updated

Nov 11, 2023

Manufacturer Information

Name

Clearstream Technologies Ltd.

Address

Moyne Upper

Enniscorthy, Wexford, 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

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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