Cardiopulmonary bypass system valve, unidirectional flow/pressure control - UK MHRA Medical Device Registration

Cardiopulmonary bypass system valve, unidirectional flow/pressure control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 113570. The device is manufactured by Quest Medical, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Emergo Consulting (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 valve, unidirectional flow/pressure control

MHRA Device ID: 113570•Ref: 113570

Device Type

General Medical Device

Devices

Cardiopulmonary bypass system valve, unidirectional flow/pressure control

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Apr 17, 2024

Manufacturer Information

Name

Quest Medical, Inc.

Address

1 Allentown Parkway

Allen, Texas, United States

Created Date

Nov 17, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Other Products from Quest Medical, Inc. (10)

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Cardiopulmonary bypass system valve, unidirectional flow/pressure control - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

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