Haemofiltration system
United Kingdom·General Medical Device·Nuwellis, Inc.·Registered Nov 26, 2024- Device ID
- 163860
- MHRA Reference Number
- 163860
- Date Registered
- Nov 26, 2024
- Last Updated
- Dec 5, 2023
- Device Type
- General Medical Device
- Devices
- Haemofiltration system
- Type
- Class IIa
- Name
- Nuwellis, Inc.
- Address
- 12988 Valley View Road Eden Prairie, Minnesota, United States
- Created Date
- Dec 29, 2022
- Relationship Type
- UK Responsible Person
- Address
- Unit 24 Cranfield Innovation Centre University Way Cranfield, Bedfordshire, England, United KingdomPostcode: MK43 0BT
Devices with a matching generic name or device type registered with MHRA
Additional devices registered by the same manufacturer
Additional devices represented by Jump Start Consulting Limited in the UK
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.