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 - Vivago Oy

Address:

Itsehallintokuja 6

Espoo

02600

Finland

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

Suite 115 Wey House

15 Church Street

Weybridge

Surrey KT13 9EW

England United Kingdom

Code/Term Type

Biomechanical function analysis/rehabilitation software Biomechanical function analysis/rehabilitation 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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