Autotransfusion system blood collection/processing pump - UK MHRA Medical Device Registration

Autotransfusion system blood collection/processing pump is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 174281. The device is manufactured by i-SEP from France, classified as General Medical Device. The authorized representative in the UK is Qserve Group 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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Autotransfusion system blood collection/processing pump

MHRA Device ID: 174281•Ref: 174281

Device Type

General Medical Device

Devices

Autotransfusion system blood collection/processing pump

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

i-SEP

Address

21 rue de la Noue Bras de Fer

Nantes, France

Created Date

Dec 15, 2022

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Autotransfusion system blood collection/processing pump - UK MHRA Medical Device Registration

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