Clinical management support software - UK MHRA Medical Device Registration

Clinical management support software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 103521. The device is manufactured by ArtiQ NV from Belgium, classified as General Medical Device. The authorized representative in the UK is Qserve Group UK, Ltd. .

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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Clinical management support software

MHRA Device ID: 103521•Ref: 103521

Device Type

General Medical Device

Devices

Clinical management support software

Type

Class IIa

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

ArtiQ NV

Address

Boskouter 15

Kessel-Lo, Vlaams-Brabant, Belgium

Created Date

Sep 9, 2021

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

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Clinical management support software - UK MHRA Medical Device Registration

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