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Haemofiltration system - UK MHRA Medical Device Registration

Haemofiltration system is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163860. The device is manufactured by Nuwellis, Inc. from United States, classified as General Medical Device. The authorized representative in the UK is Jump Start Consulting Limited.

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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General Medical Device
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Haemofiltration system
MHRA Device ID: 163860โ€ขRef: 163860

Device Type

General Medical Device

Devices

Haemofiltration system

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 5, 2023

Manufacturer Information

Address

12988 Valley View Road

Eden Prairie, Minnesota, United States

Created Date

Dec 29, 2022

Authorized Representative

Relationship Type

UK Responsible Person

Address

Unit 24 Cranfield Innovation Centre University Way

Cranfield, Bedfordshire, England, United Kingdom

Postcode: MK43 0BT

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