Peripheral angioplasty balloon catheter, drug-coated - UK MHRA Medical Device Registration

Peripheral angioplasty balloon catheter, drug-coated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 192267. The device is manufactured by Bard Peripheral Vascular, Inc. from United States, 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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General Medical Device

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Peripheral angioplasty balloon catheter, drug-coated

MHRA Device ID: 192267•Ref: 192267

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, drug-coated

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Mar 26, 2024

Manufacturer Information

Name

Bard Peripheral Vascular, Inc.

Address

1625 West 3rd Street

Tempe, Arizona, United States

Created Date

Apr 22, 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, drug-coated - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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