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 - Lumos Diagnostic Inc.

Address:

2724 Loker Avenue West

Carlsbad

California 92010

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

Multiple cell-mediated host immune response marker IVD kit rapid ICT clinical Multiple cell-mediated host immune response marker IVD kit rapid ICT clinical IVD General

Multiple-type clinical chemistry analyte profile IVD control Multiple-type clinical chemistry analyte profile IVD control 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
Multiple cell-mediated host immune response marker IVD kit rapid ICT clinical	Multiple cell-mediated host immune response marker IVD kit rapid ICT clinical	IVD General
Multiple-type clinical chemistry analyte profile IVD control	Multiple-type clinical chemistry analyte profile IVD control	IVD General