United Kingdom MHRA device registration 96411

Peripheral angioplasty balloon catheter, basic

United Kingdom flagUnited Kingdom·General Medical Device·Spectranetics Corporation - Brandin Court·Registered Sep 29, 2024
Registration details
Device ID
96411
MHRA Reference Number
96411
Date Registered
Sep 29, 2024
Last Updated
Feb 1, 2024
Device classification
Device Type
General Medical Device
Devices
Peripheral angioplasty balloon catheter, basic
Type
Class IIa
Manufacturer
Address
5055 Brandin Court
Fremont, United States
Created Date
Apr 26, 2021
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, basic is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96411. The device is manufactured by Spectranetics Corporation - Brandin Court from United States, classified as General Medical Device. The authorized representative in the UK is Philips Electronics UK Ltd.

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