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 - medaia GmbH

Address:

Am Eisernen Tor 5

Graz

Graz

Steiermark 8010

Austria

Authorised Representative/ UK Responsible Person
Name: Ilia Mallioras
Address:

39 Irene Road

London

SW6 4AP

England United Kingdom

Code/Term Type

Multidisciplinary medical image management software Multidisciplinary medical image 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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