Radiology information system application software - UK MHRA Medical Device Registration

Radiology information system application software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 139423. The device is manufactured by Anatomage, Inc. from United States, 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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Radiology information system application software

MHRA Device ID: 139423•Ref: 139423

Device Type

General Medical Device

Devices

Radiology information system application software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Anatomage, Inc.

Address

3350 Scott Blvd. #29

Santa Clara, California, United States

Created Date

Mar 10, 2022

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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Radiology information system application software - UK MHRA Medical Device Registration

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