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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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SGTi-flex COVID-19 Ag

La prueba SGTi-flex COVID-19 Ag, una prueba inmunocromatográfica rápida, basada en nanopartículas de oro, de un solo paso, para detección cualitativa de antígenos específicos de COVID-19. Permite un manejo sencillo y fiable sin necesidad de dispositivo.
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Lumipulse G SARS-CoV-2 Ag

La prueba Lumipulse G SARS-CoV-2 Ag fue diseñada para uso diagnóstico in vitro (IVD) con el sistema Lumipulse G para la detección y medición cuantitativa del antígeno del SARS-CoV-2 en hisopos nasofaríngeos o saliva humana.
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iFlash-2019-nCoV Antigen Test

La Prueba de Antígeno YHLO iFlash-2019-nCoV aplica el inmunoensayo quimioluminiscente (CLIA) para la detección cualitativa del antígeno del SARS-COV-2 en hisopos nasales o nasofaríngeos.
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Saliva Collectors

Los recolectores de saliva para las pruebas de COVID-19 en saliva permiten la recolección de muestras de saliva oral a través del tubo de recolección y garantizan una mezcla uniforme de la saliva recolectada con las soluciones de conservación, lo que garantiza la integridad del ADN/ARN.
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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 IgG/IgM Detection Kit (Colloidal Gold)

El kit de detección de IgG/IgM COVID-19 (oro coloidal) requiere una gota de muestra de sangre, suero o plasma para obtener resultados en 10 minutos. La tarjeta de prueba contiene un nuevo antígeno de coronavirus y un anticuerpo coloidal marcado con oro.
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El ID NOW fue diseñado para la detección cualitativa de enfermedades infecciosas utilizando la tecnología de amplificación isotérmica de ácidos nucleicos. El sistema presenta una gran pantalla táctil visual, mientras que su tamaño reducido ahorra espacio en el mesón.
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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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