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

Back to MHRA

Manufacturer's Devices - 3DHISTECH Kft

Address:

H-1141

Öv utca. 3.

Budapest Öv utca. 3.

Hungary

Authorised Representative/ UK Responsible Person
Name: Sysmex UK Ltd
Address:

Sysmex House Garamonde Drive

Wymbush

Milton Keynes

Buckinghamshire MK8 8DF

England United Kingdom

Code/Term Type

Histology/cytology/microbiology image-analysis interpretive software IVD Histology/cytology/microbiology image-analysis interpretive software IVD IVD General

Contact details

Freedom of information

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

© 2011 Crown Copyright. To contact us about this website, use our feedback form.