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LumiraDx UK Ltd
3, More London Riverside,
SE1 2AQ
London
United Kingdom of Great Britain and Northern Ireland
United Kingdom of Great Britain and Northern Ireland
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Media files
Our range of products
Product categories
- 03 Diagnostic tests
- 03.02 Immunochemistry testing, immunology testing
- 03.02.02 Diagnostic rapid tests
Diagnostic rapid tests
Our products
Product category: Diagnostic rapid tests
LumiraDx Point of Care Diagnostic Platform
The LumiraDx Platform is an innovative, next generation point of care system that combines a small, portable instrument, advanced low cost test strip and seamless digital connectivity. Its proprietary technology enables it to deliver exceptional point of care clinical performance, while being simple and easy to use.
Product category: Diagnostic rapid tests
LumiraDx INR Test
The LumiraDx INR Test is an enzyme kinetic assay based on Thrombin activity.
The coagulation cascade is activated by the test reagents and INR is calculated from the measured PT-time. Haematocrit is also measured on the strip to ensure patients are within the 25-55% range.
The accuracy of the LumiraDx INR Test is comparable to the ACL Elite lab reference method.
Not available in the US
The coagulation cascade is activated by the test reagents and INR is calculated from the measured PT-time. Haematocrit is also measured on the strip to ensure patients are within the 25-55% range.
The accuracy of the LumiraDx INR Test is comparable to the ACL Elite lab reference method.
Not available in the US
Product category: Diagnostic rapid tests
LumiraDx SARS CoV-2 Antigen Test
The LumiraDx SARS-CoV-2 Ag Test is a rapid microfluidic immunoassay detecting SARS-CoV-2 antigen.
The test uses nasal and nasopharyngeal swab samples to detect antigen nucleocapsid protein in under 12 minutes at point of care.
In clinical studies, the LumiraDx SARS-CoV-2 antigen test demonstrated 97.6% positive agreement versus RT-PCR in patients tested within 12 days of the onset of symptoms.
The test uses nasal and nasopharyngeal swab samples to detect antigen nucleocapsid protein in under 12 minutes at point of care.
In clinical studies, the LumiraDx SARS-CoV-2 antigen test demonstrated 97.6% positive agreement versus RT-PCR in patients tested within 12 days of the onset of symptoms.
Product category: Diagnostic rapid tests
LumiraDx SARS-CoV-2 Antibody Test
The LumiraDx SARS-CoV-2 Ab Test is a microfluidic immunofluorescence assay for qualitative detection of total antibodies to SARS-CoV-2 in human whole blood (capillary fingerstick or venous), plasma or serum for indication of recent or prior infection. Used with the LumiraDx Platform the Test delivers rapid results at the point of care.
Product category: Diagnostic rapid tests
LumiraDx D-Dimer Test
The LumiraDx D-Dimer Test is a rapid microfluidic immunoassay for quantitative determination of D-Dimer
The only D-Dimer Test providing fast, accurate, quantitative results in just 6 minutes from a fingerstick blood sample.1
Supporting confident decisions at the point of care with the LumiraDx Platform.
1. Based on current information at the time of publishing
The only D-Dimer Test providing fast, accurate, quantitative results in just 6 minutes from a fingerstick blood sample.1
Supporting confident decisions at the point of care with the LumiraDx Platform.
1. Based on current information at the time of publishing
Company news
Date
Topic
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Nov 10, 2020
Global Partnership to Introduce a Connected, Point-of-Care Diagnostic Platform for COVID-19 Antigen Testing in Africa
London, UK – LumiraDx, the next generation point-of-care diagnostic company, announced today a $32 million global partnership with Africa Union, Africa Centres for Disease Control and Prevention (Africa CDC), Africa Medical Supplies Platform (AMSP), Bill and Melinda Gates Foundation (BMGF), and Clinton Health Access Initiative (CHAI) with the support of the COVID-19 Therapeutics Accelerator, The Mastercard Foundation and The Rockefeller Foundation to expand access to fast, accurate and equitable COVID-19 testing in Africa.
Aug 31, 2020
LumiraDx COVID-19 Antigen Test Achieves CE Mark
London, UK – LumiraDx, the next-generation point of care diagnostic company, announced today that, in addition to the Emergency Use Authorization (EUA) granted by the U.S. Food and Drug Administration (FDA) on August 18, 2020, it had now also achieved CE Marking for its LumiraDx SARS-CoV-2 antigen test. The test detects antigen nucleocapsid protein from a nasal swab with results in under 12 minutes from sample application in people with COVID-19 symptoms or who are at risk of the infection. The test is the fastest, most sensitive COVID-19 antigen point of care test currently commercially available – and a crucial resource to European nations as they seek to improve access to rapid, accurate community testing.
The LumiraDx SARS-CoV-2 Ag Test is designed to be used in health care settings to provide an aid to rapid diagnosis of COVID-19. The test uses a nasal swab specimen from individuals at risk of, or with symptoms of, COVID-19 within the first 12 days of symptom onset. Clinical studies were performed at 6 sites across the US and UK with 257 subjects and demonstrated a 97.6% positive agreement and 96.6% negative agreement with RT-PCR.
The LumiraDx SARS-CoV-2 Ag Test is designed to be used in health care settings to provide an aid to rapid diagnosis of COVID-19. The test uses a nasal swab specimen from individuals at risk of, or with symptoms of, COVID-19 within the first 12 days of symptom onset. Clinical studies were performed at 6 sites across the US and UK with 257 subjects and demonstrated a 97.6% positive agreement and 96.6% negative agreement with RT-PCR.
About us
Company details
LumiraDx was founded in 2014 by a group of entrepreneurs: Ron Zwanziger, our Chairman and Chief Executive Officer; Dave Scott, Ph.D., our Chief Technology Officer; and Jerry McAleer, Ph.D., our Chief Scientist, who have a successful track record in building and scaling diagnostics businesses over three decades, including at companies such as Medisense, Inc., Inverness Medical Technology Inc. and Alere Inc. The company has raised approximately $600 million through debt and equity from institutional and strategic investors including the Bill & Melinda Gates Foundation, Morningside Ventures and U.S. Boston Capital Corporation. Based in the UK, with primary R&D and manufacturing operations in Stirling, Scotland, and supported by its worldwide affiliates to provide access in all major markets, LumiraDx has over 600 employees worldwide.
LumiraDx develops, manufactures and commercializes an innovative point-of-care diagnostic Platform. The LumiraDx Platform is designed to deliver lab comparable diagnostic results at the point of care in minutes. It is designed to be affordable and accessible for healthcare providers globally, and to strengthen community-based healthcare.
LumiraDx develops, manufactures and commercializes an innovative point-of-care diagnostic Platform. The LumiraDx Platform is designed to deliver lab comparable diagnostic results at the point of care in minutes. It is designed to be affordable and accessible for healthcare providers globally, and to strengthen community-based healthcare.