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Hemostasis Analyzers Global Market Report 2022

·4-min read

Major players in the hemostasis analyzers market are Thermo Fisher Scientific Inc, Alere Inc, Siemens AG, F-Hoffmann La Roche, Nihon Kohden Corporation, Sysmex Corporation, Helena Laboratories, International Technidyne Corporation, Instrumentation Laboratory (A Division of the Werfen Group), and Abbott.

New York, May 27, 2022 (GLOBE NEWSWIRE) -- announces the release of the report "Hemostasis Analyzers Global Market Report 2022" -

The global hemostasis analyzers market is expected to grow from $4.18 billion in 2021 to $4.52 billion in 2022 at a compound annual growth rate (CAGR) of 8.1%. The market is expected to grow to $5.97 billion in 2026 at a compound annual growth rate (CAGR) of 7.2%.

The hemostasis analyzers market consists of sales of hemostasis analyzers. Hemostasis analyzers are devices that measure clotting mechanisms of hemostasis to detect clotting deficiencies.

The main products in hemostasis analyzers are clinical laboratory analyzers, point-of-care testing analyzers, and consumables.The clinical laboratory analyzers are devices that are used to calculate the concentration of certain substances in various samples.

The hemostasis analyzers are used to perform tests such as APTT tests, D dimer tests, platelet function tests, fibrinogen tests, prothrombin time tests, and other tests using optical technology, mechanical technology, electrochemical technology, and other technologies. The various end uses involved are hospitals and clinics, diagnostic centers, research and development organizations, ambulatory surgical centers, others.

Increasing awareness regarding blood disorder conditions is driving the hemostasis analyzers market.Blood disorders such as Hemophilia and Von Willebrand disease (vWD) are genetic disorders and are not well known to people.

This results in late diagnosis of blood disorders affecting the patients.For instance, the National Haemophilia Foundation’s Red Tie Campaign is raising awareness about treatment for bleeding disorders like hemophilia, leukemia, myeloma, and lymphoma for approximately 3 million people in the USA with bleeding disorders.

The Haemophilia Foundation Australia is an organization that is working towards the wellbeing of people affected by blood disorders through education, advocacy, and the promotion of research. Increasing awareness is expected to improve the diagnosis rate of blood disorders driving the demand for hemostasis analyzers.

Recalls of defective hemostasis analyzers are acting as a restraint on the hemostasis analyzers market.A product recall is done by the manufacturer or developer of the product as a precautionary measure when safety issues or defects are discovered that can endanger the consumer.

A faulty hemostasis analyzer may provide wrong results and may cause misdiagnosis affecting consumer confidence in the analyzers. For instance, the U.S. Food and Drug Administration (FDA) recalled Siemens Healthcare Diagnostics, Inc’s automated hemostasis/ blood coagulation analyzer as the device was showing incorrect clotting time. The FDA recalled Fisher Diagnostics’ hemostasis kit due to sensitivity issues. Product recalls severely affect the revenues of manufacturers, acting as a restraint on the market.

Manufacturers of hemostasis analyzers are investing in the research and development of portable, handheld hemostasis analyzers which are convenient to be carried anywhere and are small enough to fit in a person’s palm.These portable hemostasis analyzers provide a faster and easier testing process and facilitate independent analysis of results instead of having to visit a diagnostic center.

For instance, Siemens Healthcare offers the Xprecia Stride Coagulation Analyzer which is small enough to fit inside a pocket and provides accurate results. Also, the Coatron coagulation analyzer by TECO Medical Instruments is a portable, handheld semi-automatic hemostasis analyzer.

Manufacturers of hemostasis analyzers are governed by regulatory bodies such as the Food and Drug Administration (FDA) in the USA.The FDA has classified hemostasis analyzers into the Class II category, as they have a moderate risk associated with usage.

Class II devices are bounded by device-specific regulations which include performance standards, premarket data requirements, post-market surveillance, and labeling requirements associated with device usage. The labeling of hemostasis analyzers is required to have a list of contraindications, adverse reactions, precautions, warnings, and other instructions before the equipment is released into the market.

The regions covered in this report are Asia-Pacific, Western Europe, Eastern Europe, North America, South America, Middle East, and Africa.

The countries covered in the hemostasis analyzers market are Australia, Brazil, China, France, Germany, India, Indonesia, Japan, Russia, South Korea, UK, and USA.

Read the full report:

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