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 - Visiba Group AB

Address:

Krokslätts Fabriker 61

Torsgatan 26

Mölndal

Västra Götaland 43137

Sweden

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

1 Butterwick Hammersmith

London

W68DL

England United Kingdom

Code/Term Type

Patient general health self-management software Patient general health self-management 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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