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COVID-19 Antigen Test
Rapid COVID-19 Antigen Test

The Rapid COVID-19 Antigen Test is an in vitro immunochromatographic assay for the qualitative detection of nucleocapsid protein antigen from SARS-CoV-2 in direct nasopharyngeal (NP) swab from individuals who are suspected of COVID-19 by their healthcare provider. It is intended to aid in the rapid diagnosis of SARS-CoV-2 infections.
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SARS-CoV-2 Test Kit

The SARS-CoV-2 ELITe MGB Kit is intended to determine, quantitatively and qualitatively, the presence of SARS-CoV-2 Virus RNA, responsible for the well known pathology COVID-19. In complete compliance with WHO guidelines, the kit targets two genes of SARS-CoV-2: RdRp and ORF8. The kit is CE-IVD marked, it allows the possibility of carrying out 240 Tests or 96, on the ELITe InGenius platform, the sample-to-result solution, capable of analysing up to 12 samples simultaneously and of reanalyzing them without the need for further extraction of genetic material.
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SARS-CoV-2 IgG (RBD & NP) Test
SARS-CoV-2 IgG (RBD & NP) Array

The Randox SARS-CoV-2 IgG (RBD & NP) array utilizes patented biochip technology to simultaneously detect IgG antibodies against both leading COVID-19 diagnostic antigens; Spike Receptor Binding Domain (RBD) and Nucleocapsid protein (NP). Maximum sensitivity is ensured through detection of antibodies against both proteins making the assay superior compared to other commercially available serology tests where false negative results are common. Measurement of both RBD and NP IgG antibodies also provides an opportunity to discriminate vaccinated versus naturally infected individuals based on leading vaccine candidates.
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COVID-19 Coronavirus Real Time PCR Kit
COVID-19 Coronavirus Real Time PCR Kit

COVID-19 Coronavirus Real Time PCR Kit is an In Vitro Diagnostic (IVD) reagent applying on fluorescent PCR technology and aiming at qualitatively detect Open Reading Frame gene region (ORF1a/b) and viral nucleocapsid region (N) of SARS-CoV-2 RNA from upper and lower respiratory tract specimens. Upper respiratory tract specimens include throat swab and nasopharyngeal swab. Lower respiratory tract specimens include sputum. The product is intended for use on populations suspected to have SARS-CoV-2 infection, as an aid in the diagnosis of SARS-CoV-2 infection by trained laboratory personnel on RT-PCR.
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COVID-19 Test
SGTi-flex COVID-19 Ag

The new SGTi-flex COVID-19 Ag is a one step, rapid gold nanoparticle-based immunochromatographic test for the qualitative detection of specific antigens of COVID-19. The cartridge-based lateral flow test provides results within 20-30 minutes and enables simple and reliable handling without requiring a device.
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SARS-CoV-2 Antigen Test
Lumipulse G SARS-CoV-2 Ag

The CE marked Lumipulse G SARS-CoV-2 Ag is designed for in vitro diagnostic (IVD) use with the Lumipulse G system for the detection and quantitative measurement of SARS-CoV-2 antigen in human nasopharyngeal swab or saliva. The assay is meant to be used as a diagnostic tool for the confirmation of a SARS-CoV-2 infection and utilizes proven CLEIA (chemiluminescent enzyme immunoassay) technology with results available in up to 35 minutes.
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SARS-COV-2 Antigen Test
iFlash-2019-nCoV Antigen Test

YHLO iFlash-2019-nCoV Antigen Test applies the chemiluminescent immunosassay (CLIA) for the qualitative detection of SARS-COV-2 antigen in nasal swab or nasopharyngeal swab.
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Saliva Collector for COVID-19 Saliva Test
Saliva Collectors

Saliva collectors for COVID-19 saliva tests enable collection of oral saliva samples through the collection tube and ensure uniform mixing of the collected saliva with the saliva preservation solution to ensure the integrity of DNA/RNA. It is widely used in 2019-nCoV detection, gene detection, cytology sample processing, virology cell culture, ELISA, molecular diagnostic detection, and saliva extraction of microorganisms.
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Respiratory Panel
BioFire® Respiratory 2.1 (RP2.1) Panel (EUA)

The BioFire RP2.1 Panel (EUA) uses a syndromic approach to accurately detect and identify the pathogens most commonly associated with respiratory infections. Fast and comprehensive, the BioFire RP2.1 Panel (EUA) offers a run time of about 45 minutes, enabling high efficiency and throughput on the BioFire® FilmArray® 2.0 and the BioFire® FilmArray® Torch Systems. Rapid respiratory PCR test results may enable better-informed diagnosis and treatment of patients. Quick turnaround on a broad menu of pathogens may also help clinicians make vital decisions regarding admission, isolation, cohorting, and additional diagnostic testing.
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COVID-19 IgM/IgG Test
Epithod 616 COVID-19 IgM/IgG Test Kit

The Epithod 616 COVID-19 IgM/IgG Test Kit is intended for the semi-quantitative detection of IgM and IgG antibodies to SARS-CoV-2 in whole blood, serum, and plasma from humans with a fast test time of less than two minutes. The gold nanoparticle-based immunoassay test kit is designed for use on the Epithod 616 analyzer which ensures better accuracy and improved sensitivity in analyzing results, and eliminates the risk of undesirable misreading.
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COVID-19 Rapid Test Kit
COVID-19 IgG/IgM Detection Kit (Colloidal Gold)

The COVID-19 IgG/IgM Detection Kit (Colloidal Gold) requires just one sample drop of blood, serum or plasma to deliver results in 10 minutes. The test card contains novel coronavirus antigen and colloidal gold labeled antibody used in colloidal gold labeling. The test has CE certificate and has been tested to produce a high level of accuracy.
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Molecular Diagnostics System

The ID NOW is a rapid, instrument-based, isothermal system for the qualitative detection of infectious diseases and uses isothermal nucleic acid amplification technology for providing molecular results in minutes. The intuitively designed instrument features a large visual touchscreen for displaying the results, eliminating transcription errors and the need for printing, while its small footprint saves bench space for use in any healthcare setting.
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Blood Collection Device

The VACUETTE QUICKSHIELD Safety Tube Holder is ideal for routine blood collection thanks to its user-friendly functional principle. The safety shield can be activated with one hand and is confirmed with an audible and tangible "click". The cannula is visibly anchored in the protective shield. This product offers straightforward and convenient use coupled with maximum safety. As combination product with a pre-mounted VACUETTE® VISIO PLUS needle, the VACUETTE® QUICKSHIELD Complete PLUS enables immediate visual control of blood flow to confirm successful venipuncture.
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COVID-19 lgM/IgG Test Kit
Coronavirus COVID-19 lgM/IgG Test Kit (Colloidal Gold)

The Coronavirus COVID-19 lgM/IgG Test Kit (Colloidal Gold) is suitable for in vitro qualitative determination of novel coronavirus IgM/IgG antibodies in human serum, plasma and whole blood. It can be used for preliminary screening of suspected patients with COVID-19.
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EURORealTime SARS-CoV-2 is a PCR test for the specific detection ofSARS-CoV-2, including the new variants VOC 202012/01 (B.1.1.7 lineage) and 501.V2 (B.1.351 lineage). The test enables quick and simple pathogen detection by means of reverse transcription and real-time PCR in one step, and has high sensitivity due to simultaneous detection of two SARS-CoV-2 target sequences.
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