United Kingdom MHRA device registration 92017

Peripheral angioplasty balloon catheter, basic

United Kingdom flagUnited Kingdom·General Medical Device·AV Medical Technologies Ltd.·Registered Nov 26, 2024
Registration details
Device ID
92017
MHRA Reference Number
92017
Date Registered
Nov 26, 2024
Last Updated
May 14, 2024
Device classification
Device Type
General Medical Device
Devices
Peripheral angioplasty balloon catheter, basic
Type
Class IIa
Manufacturer
Address
21B Habarzel St.
Tel Aviv , Israel
Created Date
Aug 3, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Building 9 Croxley Park
Watford, Herts, England, United Kingdom
Postcode: WD18 8WW
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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 92017. The device is manufactured by AV Medical Technologies Ltd. from Israel, classified as General Medical Device. The authorized representative in the UK is Medtronic 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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