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Peripheral angioplasty balloon catheter, basic - UK MHRA Medical Device Registration

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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Peripheral angioplasty balloon catheter, basic
MHRA Device ID: 92017•Ref: 92017

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, basic

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

May 14, 2024

Manufacturer Information

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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