Accelerator system quality assurance device - UK MHRA Medical Device Registration

Accelerator system quality assurance device is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 163662. The device is manufactured by Dosisoft SA from France, classified as General Medical Device. The authorized representative in the UK is Elekta 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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Accelerator system quality assurance device

MHRA Device ID: 163662•Ref: 163662

Device Type

General Medical Device

Devices

Accelerator system quality assurance device

Type

Class IIb

Date Registered

Nov 26, 2024

Last Updated

Apr 13, 2024

Manufacturer Information

Name

Dosisoft SA

Address

45-47 Avenue Carnot

Cachan, France

Created Date

Dec 21, 2022

Authorized Representative

Name

Elekta Ltd

Relationship Type

UK Responsible Person

Address

Cornerstone London Road

Crawley, West Sussex, United Kingdom

Postcode: RH10 9BL

DJ Fang

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Other Products from Dosisoft SA (2)

Radiation therapy software

Type: General Medical Device

Registered: Nov 26, 2024

Radiation therapy software

Type: General Medical Device

Registered: Nov 26, 2024

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Accelerator system quality assurance device - UK MHRA Medical Device Registration

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Address

DJ Fang

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