Abdominal aorta endovascular stent-graft - UK MHRA Medical Device Registration

Abdominal aorta endovascular stent-graft is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 186842. The device is manufactured by Medtronic, Inc from United States, 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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Abdominal aorta endovascular stent-graft

MHRA Device ID: 186842•Ref: 186842

Device Type

General Medical Device

Devices

Abdominal aorta endovascular stent-graft

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Dec 16, 2023

Manufacturer Information

Name

Medtronic, Inc

Address

710 Medtronic Parkway

Minneapolis, MN, United States

Created Date

Feb 2, 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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Abdominal aorta endovascular stent-graft - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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