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Radiation therapy software - UK MHRA Medical Device Registration

Radiation therapy software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 189329. The device is manufactured by Limbus AI Inc. from Canada, classified as General Medical Device. The authorized representative in the UK is Advena 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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Radiation therapy software
MHRA Device ID: 189329•Ref: 189329

Device Type

General Medical Device

Devices

Radiation therapy software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Sep 13, 2024

Manufacturer Information

Address

2431 Glamis Pl

Regina, Saskatchewan, Canada

Created Date

Oct 11, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

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