United Kingdom MHRA device registration 67461

Peripheral angioplasty balloon catheter, basic

United Kingdom flagUnited Kingdom·General Medical Device·Clearstream Technologies Ltd.·Registered Nov 26, 2024
Registration details
Device ID
67461
MHRA Reference Number
67461
Date Registered
Nov 26, 2024
Last Updated
Jul 2, 2024
Device classification
Device Type
General Medical Device
Devices
Peripheral angioplasty balloon catheter, basic
Type
Class IIa
Manufacturer
Address
Moyne Upper, Enniscorthy CO. Wexford
Wexford, Ireland
Created Date
Feb 23, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
1030 Eskdale Road Winnersh Triangle, Wokingham
Winnersh, England, United Kingdom
Postcode: RG41 5TS
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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 67461. The device is manufactured by Clearstream Technologies Ltd. from Ireland, classified as General Medical Device. The authorized representative in the UK is Becton, Dickinson U.K. Limited.

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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