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 - MeVis Medical Solutions AG

Address:

Caroline-Herschel-Straße 1

Bremen

28359

Germany

Authorised Representative/ UK Responsible Person
Name: Medes Ltd.
Address:

5 Beaumont Gate Shenley Hil

Radlett

Herts WD77AR

England United Kingdom

Code/Term Type

Image segmentation application software Image segmentation application software Class IIa

Radiology DICOM image processing application software Radiology DICOM image processing application software Class IIa

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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Code/Term		Type
Image segmentation application software	Image segmentation application software	Class IIa
Radiology DICOM image processing application software	Radiology DICOM image processing application software	Class IIa