Femoral artery compression system, manual, single-use - UK MHRA Medical Device Registration

Femoral artery compression system, manual, single-use is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 88869. 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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Femoral artery compression system, manual, single-use

MHRA Device ID: 88869•Ref: 88869

Device Type

General Medical Device

Devices

Femoral artery compression system, manual, single-use

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Jul 5, 2024

Manufacturer Information

Name

St. Jude Medical

Address

5050 Nathan Lane North

Plymouth, Minnesota, United States

Created Date

Feb 12, 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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Femoral artery compression system, manual, single-use - UK MHRA Medical Device Registration

Device Type

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Date Registered

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Address

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