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 - Glooko AB

Address:

Nellickevägen 20

Göteborg

Västra Götalands Län 412 63

Sweden

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

24 Old Queen Street

London

SW1H 9HP

England United Kingdom

Code/Term Type

Medical equipment clinical data interfacing software Medical equipment clinical data interfacing 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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