Coronary angioplasty balloon catheter, cutting/scoring - UK MHRA Medical Device Registration

Coronary angioplasty balloon catheter, cutting/scoring is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 152749. 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.

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Coronary angioplasty balloon catheter, cutting/scoring

MHRA Device ID: 152749•Ref: 152749

Device Type

General Medical Device

Devices

Coronary angioplasty balloon catheter, cutting/scoring

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)

Coronary angioplasty balloon catheter, cutting/scoring - 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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