Cardiopulmonary bypass cannula, femoral - UK MHRA Medical Device Registration

Cardiopulmonary bypass cannula, femoral is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 71620. The device is manufactured by Edwards Lifesciences LLC from United States, classified as General Medical Device. The authorized representative in the UK is Edwards Lifesciences 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 cannula, femoral

MHRA Device ID: 71620•Ref: 71620

Device Type

General Medical Device

Devices

Cardiopulmonary bypass cannula, femoral

Type

Class III

Date Registered

Nov 26, 2024

Last Updated

Jan 19, 2024

Manufacturer Information

Name

Edwards Lifesciences LLC

Address

One Edwards Way

Irvine, California, United States

Created Date

Apr 1, 2021

Authorized Representative

Name

Edwards Lifesciences Ltd

Relationship Type

UK Responsible Person

Address

3, The Sector, Newbury Business Park

Newbury, Berkshire, England, United Kingdom

Postcode: RG14 2PZ

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Other Products from Edwards Lifesciences LLC (10)

Other Products from Same Authorized Representative (10)

Cardiopulmonary bypass cannula, femoral - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

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