Haemofilter - UK MHRA Medical Device Registration

Haemofilter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163861. 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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Haemofilter

MHRA Device ID: 163861•Ref: 163861

Device Type

General Medical Device

Devices

Haemofilter

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Dec 5, 2023

Manufacturer Information

Name

Nuwellis, Inc.

Address

12988 Valley View Road

Eden Prairie, Minnesota, United States

Created Date

Dec 29, 2022

Authorized Representative

Name

Jump Start Consulting Limited

Relationship Type

UK Responsible Person

Address

Unit 24 Cranfield Innovation Centre University Way

Cranfield, Bedfordshire, England, United Kingdom

Postcode: MK43 0BT

DJ Fang

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Other Products from Nuwellis, Inc. (1)

Haemofiltration system

Type: General Medical Device

Registered: Nov 26, 2024

Other Products from Same Authorized Representative (10)

Haemofilter - 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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Haemofiltration system

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Haemofiltration system