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 - Visiopharm A/S

Address:

Agern Allé 24

Hørsholm

2970

Denmark

Authorised Representative/ UK Responsible Person
Name: Visiopharm UK Limited
Address:

Centrum House 36 Station Road

Egham

Surrey TW20 9LF

England United Kingdom

Code/Term Type

Histology/cytology/microbiology image-analysis interpretive software IVD Histology/cytology/microbiology image-analysis interpretive software IVD Class C

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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