Aortic bi-leaflet mechanical heart valve prosthesis - UK MHRA Medical Device Registration

Aortic bi-leaflet mechanical heart valve prosthesis is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 73670. The device is manufactured by St. Jude Medical from United States, classified as General Medical Device. The authorized representative in the UK is Abbott Medical UK 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 bi-leaflet mechanical heart valve prosthesis

MHRA Device ID: 73670•Ref: 73670

Device Type

General Medical Device

Devices

Aortic bi-leaflet mechanical heart valve prosthesis

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jul 3, 2024

Manufacturer Information

Name

St. Jude Medical

Address

177 County Road B East

St. Paul, Minnesota, United States

Created Date

Jan 25, 2021

Authorized Representative

Name

Abbott Medical UK Limited

Relationship Type

UK Responsible Person

Address

Elder House Central Boulevard Blythe Valley Business Park

Solihull, West Midlands, England, United Kingdom

Postcode: B90 8AJ

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Aortic bi-leaflet mechanical heart valve prosthesis - UK MHRA Medical Device Registration

Device Type

Devices

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Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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