Peripheral artery endovascular stent-graft, non-medicated - UK MHRA Medical Device Registration

Peripheral artery endovascular stent-graft, non-medicated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 67459. 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 artery endovascular stent-graft, non-medicated

MHRA Device ID: 67459•Ref: 67459

Device Type

General Medical Device

Devices

Peripheral artery endovascular stent-graft, non-medicated

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Dec 20, 2023

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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Other Products from Clearstream Technologies Ltd. (9)

Other Products from Same Authorized Representative (10)

Peripheral artery endovascular stent-graft, non-medicated - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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Peripheral artery endovascular stent-graft, non-medicated

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