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 213700. The device is manufactured by Bard Peripheral Vascular, Inc. from United States, classified as General Medical Device.

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MHRA Registered

General Medical Device

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Peripheral angioplasty balloon catheter, drug-coated

MHRA Device ID: 213700

Device Type

General Medical Device

Type

Class III

Status

DREGIY

Date Registered

Mar 20, 2025

Manufacturer Information

Name

Bard Peripheral Vascular, Inc.

Address

1625 West 3rd Street

Tempe, Arizona, United States

DJ Fang

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

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