Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Subtle Medical Inc.

Address:

880 Santa Cruz Avenue Suite 200

Menlo Park

California 94025

United States

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

United Kingdom

Code/Term Type

Radiology DICOM image processing application software Radiology DICOM image processing application software Class I

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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