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.
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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
Address
9965 Federal Drive
Colorado Springs, United States
Created Date
Feb 7, 2022
Relationship Type
Address
Ascent 1 Farnborough Aerospace Centre
Farnborough, Hampshire, England, United Kingdom
Postcode: GU14 6XW
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