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 - Access Genetics LLC

Address:

7400 Flying Cloud Drive Suite 150

Eden Prairie

Minnesota 55344

United States

Authorised Representative/ UK Responsible Person
Name: EU-UK Authorised Representative Ltd
Address:

Unit 591 Moat House

54 Bloomfield Avenue

Belfast

BT5 5 AD

Northern Ireland United Kingdom

Code/Term Type

General specimen collection kit IVD clinical General specimen collection kit IVD clinical Class A

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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