Cardiopulmonary bypass system defoamer - UK MHRA Medical Device Registration

Cardiopulmonary bypass system defoamer is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 97908. The device is manufactured by Terumo Corporation from Japan, classified as General Medical Device. The authorized representative in the UK is Terumo UK Ltd.

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 defoamer

MHRA Device ID: 97908•Ref: 97908

Device Type

General Medical Device

Devices

Cardiopulmonary bypass system defoamer

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 2, 2024

Manufacturer Information

Name

Terumo Corporation

Address

44-1, 2-chome, Hatagaya, Shibuya-ku

Tokyo, Japan

Created Date

Apr 29, 2021

Authorized Representative

Name

Terumo UK Ltd

Relationship Type

UK Responsible Person

Address

Otium House 2 Freemantle Road

Bagshot, Surrey, England, United Kingdom

Postcode: GU19 5LL

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Cardiopulmonary bypass system defoamer - UK MHRA Medical Device Registration

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Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

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