214 companies | 918 medical products

SARS-CoV-2 Pooling Test
Extensive SARS-CoV-2 Pooling

The Extensive SARS-CoV-2 Pooling is a rapid real-time PCR test cartridge, providing clear and concise results in a timely manner, direct at the point of care on the Vivalytic analyzer. The SARS-CoV-2 pooling test with lollipop swab allows for the screening of up to 15 patient samples and produces results in less than 45 minutes. Ideal for mass testing, the pooling could be done at the level of a ward, medical specialty, social bubble, or group of colleagues. It has potential for use in other settings, such as pre-operative screening, schools and universities, prisons, nursing homes, primary care, and large workplaces.
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SARS-CoV-2 Antigen Rapid Test
RapiSafe SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

The RapiSafe SARS-CoV-2 Antigen Rapid Test (Colloidal Gold) is designed for early detection of SARS-CoV-2 specific antigen from suspected COVID-19 cases. Faster and more convenient than PCR test, it does not require any special/additional instruments and delivers test results in 15 minutes.
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SARS-CoV-2 Antigen Self-Test
One Step Test for SARS-CoV-2 Antigen (Colloidal Gold)

Getein One Step Test for SARS-CoV-2 Antigen (Colloidal Gold) is intended for the qualitative detection of SARS-CoV-2 antigens in human nasal swab samples. The test is suitable for medical laypersons as a self-test at home or at work.
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SARS-CoV-2 Control

The VIROCLEAR SARS-CoV-2 (IVD/CE Mark) is an unassayed, non-reactive quality control for the qualitative determination of total IgG/IgM and IgG antibodies to SARS-CoV-2.
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The Agilent SARS-CoV-2 qRT-PCR Dx kit is a real-time reverse transcriptase PCR (qRT-PCR) in vitro diagnostic reagent kit for the qualitative detection of SARS-CoV-2 RNA. RNA is isolated and purified from nasopharyngeal, nasal, and oropharyngeal swab specimens obtained from individuals suspected of having COVID-19 by their healthcare provider. Clinical laboratories can easily generate diagnostic results from this single-tube assay.
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Flu A/B & SARS-CoV-2 Real-Time RT-PCR Test
DiaPlexQ Flu A/B & SARS-CoV-2

DiaPlexQ Flu A/B & SARS-CoV-2 is a Real-time RT-PCR test for the qualitative detection of HA gene from Influenza A/B virus and N and ORF1a gene from SARS-CoV-2 in nasopharyngeal swab.
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EURORealTime SARS-CoV-2 is a PCR test for the specific detection of SARS-CoV-2, including the variants alpha (B.1.1.7 lineage), beta (B.1.351 lineage), gamma (P.1 lineage), delta (B1.617.2 lineage), lambda (C.37 lineage), mu (B.1.621 lineage) and omicron (B.1.1.529 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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Sample Collection & Transport Kit
MicroTest Universal Kits

The MicroTest Universal Kits help maintain organism viability and counts for verification studies, quality control procedures, and repeat testing of viruses, chlamydiae, mycoplasma and ureaplasma with quality media, proven collection and transport tools, and safe, reliable packaging. The kits come in four media formulations and include one plastic shaft traditional-tipped polyester swab and one stainless steel shaft micro-tipped polyester swab and a 6 x 9 inches zip-seal bag for safe transport.
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SARS-CoV-2/Influenza A, B and RSV Test

REALQUALITY ResP-Aria is a kit for the identification of respiratory viruses SARS-CoV-2, Influenza A, Influenza B and RSV and their timely differential diagnosis, allowing for early therapeutic treatment and at the same time limiting the spread of COVID-19. The automatic format of the REALQUALITY ResP-Aria kit, especially for high throughputs, is supported by the GENEQUALITY X120 automatic platform, version with 96 extractions and PCR plate set-up.
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SARS CoV-2/Flu/RSV Test
Xpert Xpress CoV-2/Flu/RSV plus

The Xpert Xpress CoV-2/Flu/RSV plus enables actionable detection of SARS-CoV-2 in as little as 25 minutes, with results for all four pathogens in just 36 minutes. It offers a robust design with three distinct gene targets for SARS-CoV-2: N2, E, RdRP to offer broader coverage against mutations.
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Calibration Verification/Linearity & Daily QC Product
Control FD COVID-19 Antigen – Nucleocapsid

Control FD COVID-19 Antigen – Nucleocapsid is a calibration verification/linearity and daily quality control product that is intended to simulate negative and positive human patient samples. The stable, bi-level control for use with assays is designed to produce qualitative results for COVID-19 Antigen (Nucleocapsid) and has an open vial stability of 14 days when stored at 2-8°C.
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COVID-19 Immunoassay Kit
KAYA17 COVID Assay Kit

KAYA17 provides a complete immunoassay test kit that contains all disposables and reagents and controls needed, in packs of 25 or 50 tests. Its proprietary reagents are fine-tuned for ease of use by staff with minimal training while maintaining high sensitivity and specificity.
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COVID-19 Assay
Novodiag COVID-19 Assay

The Novodiag COVID-19 assay, performed with the Novodiag System, is a cartridge-based RT-PCR test for qualitative detection of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). The CE marked test uses nasopharyngeal swab samples from patients and delivers clinical confidence in approximately an hour.
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SARS-CoV-2 IgG Antibodies Anti-S1 Assay
iRapid SARS-CoV-2 Quant "Neutralizing" Ab

The iRapid SARS-CoV-2 Quant "Neutralizing" Ab is intended for the semi-quantitative determination of IgG antibodies anti-S1 (RBD) of SARS-CoV-2 virus as an aid in the determination of the immune reaction to SARS-CoV-2 or to the vaccine.
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Actim ELISA SARS-CoV-2 IgG offers laboratories a reliable and efficient method for mass testing of recent COVID-19 infection providing essential data for disease control measures, pandemic analysis and scientific research in just hours. The test detects recent COVID-19 infection from serum samples by measuring the specific immune reaction against the virus. The highly sensitive and specific test can be used, for example, to obtain critical information about the prevalence of COVID-19 at the population level, or to measure induced immune response during vaccine development.
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