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 - Data Innovations LLC

Address:

463 Mountainview Drive

Colchester

Vermont 05446

United States

Authorised Representative/ UK Responsible Person
Name: MT Promedt Consulting Ltd
Address:

Beaver House 23-38 Hythe Bridge Street

Oxford

OX1 2EP

England United Kingdom

Code/Term Type

Clinical laboratory information system application software Clinical laboratory information system application software IVD General

Laboratory instrument/analyser application software IVD Laboratory instrument/analyser application software IVD IVD General

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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Code/Term		Type
Clinical laboratory information system application software	Clinical laboratory information system application software	IVD General
Laboratory instrument/analyser application software IVD	Laboratory instrument/analyser application software IVD	IVD General