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 - Kaiku Health Oy

Address:

Siltasaarenkatu 12

Helsinki

00530

Finland

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

Cornerstone London Road

Crawley

West Sussex RH10 9BL

United Kingdom

Code/Term Type

Medical equipment clinical data interfacing software Medical equipment clinical data interfacing 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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