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 203710. The device is manufactured by Densitas Inc. from Canada, classified as General Medical Device. The authorized representative in the UK is AF PHARMA SERVICE 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 DICOM image processing application software

MHRA Device ID: 203710•Ref: 203710

Device Type

General Medical Device

Devices

Radiology DICOM image processing application software

Type

Class I

Date Registered

Nov 26, 2024

Last Updated

Oct 25, 2024

Manufacturer Information

Name

Densitas Inc.

Address

#66, 1344 Summer Street, Suite 311B

Halifax, Nova Scotia, Canada

Created Date

Oct 23, 2024

Authorized Representative

Name

AF PHARMA SERVICE UK LTD

Relationship Type

UK Responsible Person

Address

Suite 140 Temple Chambers 3-7 Temple Avenue

London, England, United Kingdom

Postcode: EC4Y 0DA

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Other Products from Densitas Inc. (1)

Radiology DICOM image processing application software

Type: General Medical Device

Registered: Oct 27, 2024

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

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