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 - bio.logis digital health GmbH

Address:

Altenhöferallee 3

Frankfurt am Main

Darmstadt 60438

Germany

Authorised Representative/ UK Responsible Person
Name: Mantara Health Ltd
Address:

The Grainger Suite Regent Centre

Dobson House

Newcastle Upon Tyne

Northumberland NE3 3PF

England United Kingdom

Code/Term Type

Human genomic analysis interpretive software Human genomic analysis interpretive 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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