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Hologic

Designs and provides products for clinical laboratory and blood screening, including testing items for detection of human diseases, such as tuberculosis, strep throat, pneumonia, and sexually transmitted diseases, as well as for human immunodeficiency virus type 1 (HIV-1) and hepatitis C virus (HCV) contamination of bloo ...
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Covid-19 Hologic

Clinical Laboratory

SARS-CoV-2 Test
SARS-CoV-2 Trifecta

The SARS-CoV-2 Trifecta for SARS-CoV-2 testing has superior sensitivity and simplifies workflow as it can be collected and loaded directly on the Panther system without uncapping or specimen transfer. The test allows to deliver more results in less time with a high-throughput fully automated instrument.
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Direct Load Tube Collection Kit
Direct Load Tube Collection Kit

The Direct Load Tube Collection Kit transforms specimen processing for COVID testing by eliminating the need for uncapping and specimen transfer. Labs can expedite their SARS-CoV-2 workflow with the collection device that loads directly on the Panther system.
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Direct Load Capture Cap Collection Kit
Direct Load Capture Cap Collection Kit

The Direct Load Capture Cap Collection Kit transforms specimen processing for COVID testing by eliminating the need for uncapping and specimen transfer. Labs can expedite their SARS-CoV-2 workflow with the collection device that loads directly on the Panther system.
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SARS-CoV-2 Assay
Panther Fusion SARS-CoV-2 assay

The Panther Fusion SARS-CoV-2 assay is a real-time PCR in vitro diagnostic test utilizing Hologic's proprietary TMA technology for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from nasopharyngeal, nasal and oropharyngeal swab specimens and lower respiratory tract specimens obtained from individuals who meet COVID-19 clinical and/or epidemiological criteria. The assay runs on both Hologic's Panther® and Panther Fusion systems®, enabling labs to run over 10,00 tests in 24 hours and attain first results in 3.5 hours or less.
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SARS-CoV-2 Assay
Aptima SARS-CoV-2 assay

The Aptima SARS-CoV-2 assay is an in vitro diagnostic test utilizing Hologic's proprietary TMA technology for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from nasopharyngeal, nasal and oropharyngeal swab specimens obtained from individuals who meet COVID-19 clinical and/or epidemiological criteria. The assay runs on both Hologic's Panther® and Panther Fusion systems®, enabling labs to run over 10,00 tests in 24 hours and attain first results in 3.5 hours or less.
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News of Hologic

Hologic Acquires European Molecular Diagnostic Company Diagenode

02 Mar 2021
Hologic Acquires European Molecular Diagnostic Company Diagenode
Hologic, Inc. (Marlborough, MA, USA) has acquired Diagenode (Liège, Belgium), a developer and manufacturer of molecular diagnostic assays and epigenetics products, which is expected to diversify its diagnostic business across test menu, customer segments and geography.
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Hologic Partners with Google Cloud to Focus on AI and Machine Learning for Advancing Digital Diagnostic Capabilities

04 Feb 2021
Hologic Partners with Google Cloud to Focus on AI and Machine Learning for Advancing Digital Diagnostic Capabilities
Hologic, Inc. (Marlborough, MA, USA) and Google Cloud have entered into a new agreement to focus on enhancing artificial intelligence (AI) and machine learning (ML) to bring about breakthrough results in cervical cancer screening.
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Hologic to Acquire Diagnostic Tests Provider Biotheranostics

07 Jan 2021
Hologic to Acquire Diagnostic Tests Provider Biotheranostics
Hologic, Inc. (Marlborough, MA, USA) has agreed to acquire Biotheranostics, Inc. (San Diego, CA, USA), a privately held, commercial-stage company that provides molecular diagnostic tests for breast and metastatic cancers, for approximately USD 230 million.
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Hologic Acquires SOMATEX Medical Technologies

05 Jan 2021
Hologic Acquires SOMATEX Medical Technologies
Hologic, Inc. (Marlborough, MA, USA) has completed the acquisition of SOMATEX Medical Technologies GmbH (Berlin, Germany), a leader in biopsy site markers and localization technologies, for approximately USD 64 million.
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Hologic Receives FDA Clearance for Genius AI Detection Technology for Early Breast Cancer Detection

02 Dec 2020
Hologic Receives FDA Clearance for Genius AI Detection Technology for Early Breast Cancer Detection
Hologic, Inc. (Marlborough, MA, USA) has received US Food and Drug Administration (FDA) clearance for its Genius AI Detection technology, a new deep learning-based software designed to help radiologists detect subtle potential cancers in breast tomosynthesis images.
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Hologic Showcased Latest Advances at Virtual ECR Congress 2020

20 Aug 2020
Hologic Showcased Latest Advances at Virtual ECR Congress 2020
Hologic, Inc. (Marlborough, MA, USA) showcased its latest advances and shared its new innovations on its virtual booth at the online ECR 2020 event held on July 15-21.
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Hologic to Sell Blood-Screening Business to Grifols for USD 1.85 Billion

15 Dec 2016
Hologic to Sell Blood-Screening Business to Grifols for USD 1.85 Billion
US medical device maker Hologic, Inc. has agreed to sell off its share of the Procleix blood-screening business to long-time partner, Grifols SA, for USD 1.85 billion in cash.
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About Hologic

Number of Employees: 1000+
Year of Establishment: 1986
Designs and provides products for clinical laboratory and blood screening, including testing items for detection of human diseases, such as tuberculosis, strep throat, pneumonia, and sexually transmitted diseases, as well as for human immunodeficiency virus type 1 (HIV-1) and hepatitis C virus (HCV) contamination of blood supply
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SARS-CoV-2 Assay

SARS-CoV-2 Assay

Model: Panther Fusion SARS-CoV-2 assay
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Description:

The Panther Fusion SARS-CoV-2 assay is a real-time PCR in vitro diagnostic test utilizing Hologic's proprietary TMA technology for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from nasopharyngeal, nasal and oropharyngeal swab specimens and lower respiratory tract specimens obtained from individuals who meet COVID-19 clinical and/or epidemiological criteria.
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Full Description Features

Description

The Panther Fusion SARS-CoV-2 assay is a real-time PCR in vitro diagnostic test utilizing Hologic's proprietary TMA technology for the qualitative detection of RNA from SARS-CoV-2 isolated and purified from nasopharyngeal, nasal and oropharyngeal swab specimens and lower respiratory tract specimens obtained from individuals who meet COVID-19 clinical and/or epidemiological criteria. The assay runs on both Hologic's Panther® and Panther Fusion systems®, enabling labs to run over 10,00 tests in 24 hours and attain first results in 3.5 hours or less. Request Information

Features

•Fully automated from sample-to-result, with easy to interpret results.

•Run multiple assays from one specimen.

•Detect and differentiate between other respiratory illnesses.

•Run alongside other PCR and TMA assays simultaneously. Request Information

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