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 199903. The device is manufactured by Clearstream Technologies Ltd. from Ireland, classified as General Medical Device. The authorized representative in the UK is Becton, Dickinson U.K. 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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Peripheral angioplasty balloon catheter, basic

MHRA Device ID: 199903•Ref: 199903

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Jul 2, 2024

Manufacturer Information

Name

Clearstream Technologies Ltd.

Address

Moyne Upper, Enniscorthy CO. Wexford

Wexford, Ireland

Created Date

Feb 23, 2021

Authorized Representative

Name

Becton, Dickinson U.K. Limited

Relationship Type

UK Responsible Person

Address

1030 Eskdale Road Winnersh Triangle, Wokingham

Winnersh, England, United Kingdom

Postcode: RG41 5TS

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

Device Type

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Date Registered

Last Updated

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Created Date

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