United Kingdom MHRA device registration 91304

Whole-blood-recovery autotransfusion system, manual

United Kingdom·General Medical Device·Redax S.p.A·Registered Nov 26, 2024

Registration details

Device ID: 91304
MHRA Reference Number: 91304
Date Registered: Nov 26, 2024
Last Updated: Aug 7, 2024

Device classification

Device Type: General Medical Device
Devices: Whole-blood-recovery autotransfusion system, manual
Type: Class IIa

Manufacturer

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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About this record

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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