Aortic transcatheter heart valve bioprosthesis, stent-like framework - UK MHRA Medical Device Registration

Aortic transcatheter heart valve bioprosthesis, stent-like framework is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 179898. The device is manufactured by Medtronic CoreValve LLC 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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Aortic transcatheter heart valve bioprosthesis, stent-like framework

MHRA Device ID: 179898•Ref: 179898

Device Type

General Medical Device

Devices

Aortic transcatheter heart valve bioprosthesis, stent-like framework

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Dec 28, 2023

Manufacturer Information

Name

Medtronic CoreValve LLC

Address

1851 E. Deere Ave.

Santa Ana, United States

Created Date

Mar 26, 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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Other Products from Medtronic CoreValve LLC (10)

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Aortic transcatheter heart valve bioprosthesis, stent-like framework - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

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DJ Fang

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