United Kingdom MHRA device registration 155445

Peripheral angioplasty balloon catheter, drug-coated

United Kingdom flagUnited Kingdom·General Medical Device·Philips Image Guided Therapy Corporation·Registered Nov 26, 2024
Registration details
Device ID
155445
MHRA Reference Number
155445
Date Registered
Nov 26, 2024
Last Updated
Nov 16, 2024
Device classification
Device Type
General Medical Device
Devices
Peripheral angioplasty balloon catheter, drug-coated
Type
Class III
Manufacturer
Address
9965 Federal Drive
Colorado Springs, United States
Created Date
Feb 7, 2022
Authorized Representative
Relationship Type
UK Responsible Person
Address
Ascent 1 Farnborough Aerospace Centre
Farnborough, Hampshire, England, United Kingdom
Postcode: GU14 6XW
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About this record

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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