Red blood cell-recovery autotransfusion system - UK MHRA Medical Device Registration

Red blood cell-recovery autotransfusion system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163229. 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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Red blood cell-recovery autotransfusion system

MHRA Device ID: 163229

Device Type

General Medical Device

Devices

Red blood cell-recovery autotransfusion system

Type

Class I

Date Registered

Dec 15, 2022

Last Updated

Dec 22, 2022

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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Other Products from i-SEP (10)

Other Products from Same Authorized Representative (10)

Red blood cell-recovery autotransfusion system - UK MHRA Medical Device Registration

Device Type

Devices

Type

Date Registered

Last Updated

Name

Address

Created Date

Name

Relationship Type

Address

DJ Fang

Compression/pressure sock/stocking, single-use

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Blood transfusion filter

Red blood cell-recovery autotransfusion system

Red blood cell-recovery autotransfusion system

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