Peripheral angioplasty balloon catheter, drug-coated - UK MHRA Medical Device Registration

Peripheral angioplasty balloon catheter, drug-coated is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 70523. The device is manufactured by Invatec SpA from Italy, 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, drug-coated

MHRA Device ID: 70523•Ref: 70523

Device Type

General Medical Device

Devices

Peripheral angioplasty balloon catheter, drug-coated

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 28, 2023

Manufacturer Information

Name

Invatec SpA

Address

Via Martiri della Liberta 7 Roncadelle

Brescia, Italy

Created Date

Mar 25, 2021

Authorized Representative

Name

Medtronic Limited

Relationship Type

UK Responsible Person

Address

Building 9 Croxley Park

Watford, Herts, England, United Kingdom

Postcode: WD18 8WW

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Peripheral angioplasty balloon catheter, drug-coated - UK MHRA Medical Device Registration

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