Cardiopulmonary bypass system centrifugal pump - UK MHRA Medical Device Registration

Cardiopulmonary bypass system centrifugal pump is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 77998. The device is manufactured by Thoratec Switzerland GmbH from Switzerland, 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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Cardiopulmonary bypass system centrifugal pump

MHRA Device ID: 77998•Ref: 77998

Device Type

General Medical Device

Devices

Cardiopulmonary bypass system centrifugal pump

Type

Class IIb

Date Registered

Apr 11, 2024

Last Updated

Mar 1, 2024

Manufacturer Information

Name

Thoratec Switzerland GmbH

Address

Technoparkstrasse 1

Zurich , Switzerland

Created Date

Apr 29, 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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Cardiopulmonary bypass system centrifugal pump - UK MHRA Medical Device Registration

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Address

Created Date

Name

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