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 181046. 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.

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Haemofiltration system

MHRA Device ID: 181046•Ref: 181046

Device Type

General Medical Device

Devices

Haemofiltration system

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Oct 24, 2024

Manufacturer Information

Name

Medica S.p.A.

Address

Via degli Artigiani 7

Medolla, Italy

Created Date

Oct 31, 2023

Authorized Representative

Name

MedEnvoy UK Limited

Relationship Type

UK Responsible Person

Address

85 Great Portland Street First Floor

London, England, United Kingdom

Postcode: W1W 7LT

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Haemofiltration system - UK MHRA Medical Device Registration

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