In Vitro Diagnostics (IVD) include reagents, instruments, and systems intended for use in the diagnosis of disease or other conditions, including the determination of the state of health, in order to treat or prevent disease. The reagents, instruments and systems are intended for use in the collection, preparation, and examination of specimens taken from the human body. The categories tracked under this market are Cardiac Disease, Hematological Disorders, Hormonal Disorders, Metabolic Disorder, Infectious Disease, IVD Analyzers and Reagents, Oncology and Reproductive Health Diagnostics. Influenza Tests are laboratory based tests used to identify active or suspected influenza infections, using a combination of molecular diagnostics and immunoassay. GlobalData uses proprietary data and analytics to provide a comprehensive report on the influenza tests devices market, including market shares of different players within the US. Buy the latest report here.

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In 2022, GlobalData’s Market Model methodology determined that the leading player in the influenza tests market in the US was Abbott Laboratories followed by Quidelortho, Becton Dickinson and Co, Danaher, F. Hoffmann-La Roche, Sekisui Diagnostics, DiaSorin and Thermo Fisher Scientific.

This segment includes Influenza Antigen Tests, Influenza Multiplex NAATs, and Influenza Lowplex Nucleic Acid Amplification Tests (NAATs)

Following the widespread disruption resulting from the COVID-19 pandemic to the broader medical devices market during 2020 and 2021, the value of the influenza tests devices market within the US was expected to be over $30m in 2022.

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The medical devices pipeline data used in this article were obtained from the Medical Pipeline Products Database of GlobalData’s Medical Intelligence Center. Pipeline Products database is a comprehensive source of information on medical devices, it covers 39K products which are in development stage and intended for diagnosis, treatment, and management of diseases/conditions/symptoms directly or indirectly. The pipeline products included in the database are sourced from reliable and authenticated sources, such as company websites, SEC filings, conference presentations, analyst presentations, news releases, clinical trial registries, and grants. The information is collected by following systematic research techniques and proprietary methodology.