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 181050. The device is manufactured by Medica S.p.A. from Italy, classified as General Medical Device. The authorized representative in the UK is MedEnvoy UK 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.
Device Type
General Medical Device
Devices
Haemofiltration system
Type
Class IIb
Date Registered
Nov 26, 2024
Last Updated
Oct 24, 2024
Relationship Type
Address
85 Great Portland Street First Floor
London, England, United Kingdom
Postcode: W1W 7LT
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