United Kingdom MHRA device registration 160520

Peripheral angioplasty balloon catheter, basic

United Kingdom·General Medical Device·Clearstream Technologies Ltd.·Registered Jul 8, 2024

Registration details

Device ID: 160520
MHRA Reference Number: 160520
Date Registered: Jul 8, 2024
Last Updated: Nov 11, 2023

Device classification

Device Type: General Medical Device
Devices: Peripheral angioplasty balloon catheter, basic
Type: Class IIa

Manufacturer

Name: Clearstream Technologies Ltd.
Address: Moyne Upper
Enniscorthy, Wexford, Ireland
Created Date: Nov 14, 2022

Authorized Representative

Name: Cordis Medical UK Limited
Relationship Type: UK Responsible Person
Address: Suite 402, Chadwick House Birchwood Park
Warrington, England, United Kingdom
Postcode: WA3 6AE

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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 160520. The device is manufactured by Clearstream Technologies Ltd. from Ireland, classified as General Medical Device. The authorized representative in the UK is Cordis Medical UK 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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