United Kingdom MHRA device registration 163220

Red blood cell-recovery autotransfusion system

United Kingdom·General Medical Device·i-SEP·Registered Dec 15, 2022

Registration details

Device ID: 163220
Date Registered: Dec 15, 2022
Last Updated: Dec 22, 2022

Device classification

Device Type: General Medical Device
Devices: Red blood cell-recovery autotransfusion system
Type: Class IIb

Manufacturer

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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Red blood cell-recovery autotransfusion systemDec 15, 2022

Type: General Medical Device

Device ID: 163227

Red blood cell-recovery autotransfusion systemDec 15, 2022

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Device ID: 163226

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About this record

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 163220. 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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