Radiology DICOM image processing application software - UK MHRA Medical Device Registration

Radiology DICOM image processing application software is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 130483. The device is manufactured by FUJIFILM Italia S.p.A from Italy, classified as General Medical Device. The authorized representative in the UK is Fujifilm Healthcare 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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Radiology DICOM image processing application software

MHRA Device ID: 130483•Ref: 130483

Device Type

General Medical Device

Devices

Radiology DICOM image processing application software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Apr 20, 2024

Manufacturer Information

Name

FUJIFILM Italia S.p.A

Address

Strada Statale 11 Padana Superiore 2/B

Cernusco sul Naviglio (MI), Italy

Created Date

Jan 1, 2022

Authorized Representative

Name

Fujifilm Healthcare UK Limited

Relationship Type

UK Responsible Person

Address

Fujifilm House Whitbread Way

Bedford, England, United Kingdom

Postcode: MK42 0ZE

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Other Products from FUJIFILM Italia S.p.A (1)

Radiological PACS software

Type: General Medical Device

Registered: Mar 28, 2025

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Radiology DICOM image processing application software - UK MHRA Medical Device Registration

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