Whole-blood-recovery autotransfusion system, manual - UK MHRA Medical Device Registration

Whole-blood-recovery autotransfusion system, manual is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 91304. The device is manufactured by Redax S.p.A from Italy, classified as General Medical Device. The authorized representative in the UK is Advena 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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Whole-blood-recovery autotransfusion system, manual

MHRA Device ID: 91304•Ref: 91304

Device Type

General Medical Device

Devices

Whole-blood-recovery autotransfusion system, manual

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Aug 7, 2024

Manufacturer Information

Name

Redax S.p.A

Address

via Galileo Galileo 18 Poggio Rusco

Mantova, Italy

Created Date

Jul 30, 2021

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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Whole-blood-recovery autotransfusion system, manual - 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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