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 155445. The device is manufactured by Philips Image Guided Therapy Corporation from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

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, drug-coated

MHRA Device ID: 155445•Ref: 155445

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, drug-coated

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Nov 16, 2024

Manufacturer Information

Name

Philips Image Guided Therapy Corporation

Address

9965 Federal Drive

Colorado Springs, United States

Created Date

Feb 7, 2022

Authorized Representative

Name

Philips Electronics UK Ltd

Relationship Type

UK Responsible Person

Address

Ascent 1 Farnborough Aerospace Centre

Farnborough, Hampshire, England, United Kingdom

Postcode: GU14 6XW

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Other Products from Philips Image Guided Therapy Corporation (3)

Other Products from Same Authorized Representative (10)

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

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Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

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DJ Fang

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