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Disposable Protective Suit For Medical Use
Disposable Protective Suit For Medical Use

Perry Health’s Disposable Protective Suit For Medical Use are made of non-woven fabric with film and undergo sterilization treatment by use of ethylene oxide. The protective equipment for medical staff is FDA as well as CE certified and comes in a packing of one piece (individual polybag) and 30 pieces per carton.
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SARS-COV-2 Variants RT- PCR Test
SARS-COV-2 Variants Real Time PCR Kit

The SARS-COV-2 Variants Real Time PCR kit uses real-time reverse transcription and amplification of nucleic acids in one step for the detection of SARS-CoV-2 and identification of the main SARS-CoV-2 variants of concern.
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SARS-CoV-2 Ag Assay
LIAISON SARS-CoV-2 Ag

The LIAISON SARS-CoV-2 Ag assay is a chemiluminescence sandwich-immunoassay (CLIA) based technology for the quantitative determination of Nucleocapsid antigen protein from SARS-CoV-2 samples - in nasal swab (NS), nasopharyngeal swab (NPS) eluted in UTM/VTM directly from individuals who are suspected of COVID-19 by their healthcare provider within the first 10 days of the onset of symptoms. The assay is a unique quantitative solution to detect suspected COVID-19 patients, do contact tracing and rapidly implement isolation procedures for those patients who have been infected and might be able to spread SARS-CoV-2.
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COVID-19 Antigen Saliva Rapid Test
GLINE-2019-nCoV Antigen Saliva Rapid Test

The GLINE-2019-nCoV Antigen Saliva is a rapid antigen salivary test that detects nucleocapsid protein of the SARS-CoV-2 virus based on colloidal gold immunochromatography assay (CGIA). The assay is more acceptable by users and makes home-testing possible.
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SARS-CoV-2 RT-PCR Assay
GSD NovaType II SARS-CoV-2

The GSD NovaType II SARS-CoV-2 Real-Time RT-PCR assay allows for the identification of relevant mutations associated with SARS-CoV-2 variants: B.1.1.7 (UK), B.1.351 (South Africa), and B.1.1.28 (P.1) (Brazil). The assay is intended as a confirmatory test for potential mutants and should only be performed after first testing patient specimens for the presence of SARS-CoV-2 RNA with a CE-IVD marked screening assay such as the GSD NovaPrime SARS-CoV-2 (COVID-19) RT-PCR kit.
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SARS-CoV-2 IgG Assays
Atellica IM and ADVIA Centaur SARS-CoV-2 IgG (sCOVG) Assays

Both the Atellica IM and the ADVIA Centaur SARS-CoV-2 IgG (sCOVG) assays measure IgG antibodies to SARS-CoV-2 in the blood to help clinicians assess the level of an individual's immune response over time. The assays produce results rapidly in as few as 25 minutes on the Atellica IM Analyzer and enable accurate antibody testing on a large scale for both reference laboratories and acute care settings.
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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
SARS-CoV-2 ELITe MGB 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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PRUEBA PARA LA COVID-19
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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PRUEBA DE ANTÍGENO SARS-COV-2
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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COLECTOR DE SALIVA PARA LA PRUEBA DE COVID-19
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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