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Rapid Tests
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COVID-19 ANTIGEN RAPID TEST
COVID-19-CHECK-1 ANTIGEN

The COVID-19-CHECK-1 ANTIGEN is an immunochromatographic rapid test for the qualitative detection of SARS-CoV-2 virus in nasopharyngeal swab samples. The COVID-19-CHECK-1 Antigen qualitative immunochromatographic rapid test is to be used for the detection of the SARS-CoV-2 virus from nasopharyngeal swab samples by healthcare medical professionals.
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SARS-CoV2 Antigen Rapid Test
SARS-CoV2 Antigen Rapid Test

Monocent SARS-CoV2 Antigen Rapid test is a qualitative and immunochromatographic in vitro assay for the detection of SARS-CoV2 virus from nasal swab or nasopharyngeal swab obtained from patient with signs and symptoms of respiratory infection. It can detect the presence of SARS-CoV2 viral nucleocapsid (N) protein in nasal or nasopharyngeal specimen at very low concentration without any high dose hook effect. The CE-IVD kit includes all the necessary tools needed to run the test for 25 patients, such as cassettes, buffer, nasopharyngeal swabs, tubes with dropper caps and IFU.
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Nucleic Acid Extraction Kit
MGIEasy Nucleic Acid Extraction Kit

The MGIEasy Nucleic Acid Extraction Kit is designed for isolating viral DNA and RNA from various sample types using super paramagnetic bead technology, the extracted nucleic acid is applicable for the downstream molecular detection, such as PCR, real time-PCR or Sequencing. The kit is compatible with MGISP-960 and MGISP-100, which can extract up to 192 samples per run.
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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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Novel Corona Virus (SARS-CoV-2) Ag Rapid Test Kit
Novel Corona Virus (SARS-CoV-2) Ag Rapid Test Kit (20T/25T/50T)

The Bioperfectus Technologies Novel Corona Virus(SARS-CoV-2)Ag Rapid Test Kit is a rapid chromatographic immunoassay for the qualitative detection of SARS-CoV-2 nucleocapsid antigens in nasopharyngeal swabs from individuals who are suspected of COVID-19 within the first seven days of the onset of symptoms.
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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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SARS-CoV-2 Research Panel
Ion AmpliSeq SARS-CoV-2 Research Panel

The Ion AmpliSeq SARS-CoV-2 Research Panel consists of two pools with amplicons ranging from 125 bp to 275 bp in length and covers >99% of the SARS-CoV-2 genome, including all serotypes. The assay is part of a fast, automated, and accurate targeted NGS workflow that enables coronavirus typing in under a day. This end-to-end solution includes the assay and plug-in suite that was developed in collaboration with researchers at the forefront of the SARS-CoV-2 crisis.
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SARS-CoV-2 Test
Allplex 2019-nCoV Assay

The Allplex 2019-nCoV Assay is a multiplex Real-time PCR assay for the simultaneous detection of three target genes of SARS-CoV-2 in a single tube. The assay is designed to detect RdRP and N genes specific for SARS-CoV-2, and E gene for all of Sarbecovirus, including SARS-CoV-2.
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SARS-CoV-2 (COVID-19) Test
GSD NovaPrime® SARS-CoV-2 (COVID-19) RT-PCR

The GSD NovaPrime® SARS-CoV-2 (COVID-19) RT-PCR is intended for the qualitative determination of SARS-CoV-2 (Severe acute respiratory syndrome coronavirus 2) genomic RNA extracted from human respiratory (nasal wash/swab, nasopharyngeal wash/swab, oropharyngeal swab and bronchoalveolar lavage) specimen types. The assay simultaneously detects two target sequences inside the N gene while the multiplex PCR allows a streamlined workflow in one reaction and provides results in approximately two hours.
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SARS-CoV-2 (COVID-19) Test
Vivalytic Viral Respiratory Tract Infection (VRI) Array

The Vivalytic Viral Respiratory Tract Infection Array Detecting SARS-CoV-2 (COVID-19) can identify SARS-CoV-2 (COVID-19) and differentiate it from nine other respiratory infections with similar symptoms, including influenza and all known coronaviruses. One of the world’s first multiplex molecular diagnostic tests to meet the COVID-19 testing recommendations of the World Health Organization (WHO) and the Centers for Disease Control (CDC), it provides a more comprehensive respiratory screening which enables precise and informed treatment decisions to be made.
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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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Reagents
HemosIL reagents

HemosIL reagents are a comprehensive panel of fully automated Hemostasis assays, designed for disease-state management and enhancing efficiency of lab operations and ultimately, patient care. From routine to specialty testing, HemosIL reagents deliver fast, accurate results, and eliminate reconstitution time, acclimation time and repetitive manual pipetting.
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HPV Diagnostic Test
PapilloCheck

The PapilloCheck is a CE-certified in-vitro diagnostic kit (CE-IVD) for the qualitative detection and genotyping of 24 pathogenic HPV types (18 high-risk and 6 low-risk types) in DNA preparations from human cervical smears. The assay is based on detection and identification of a fragment of the viral E1 gene using a DNA microarray and allows the simultaneous processing of 12 cervical samples.
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HTLV-I/II Immunoreaction Cartridges
Lumipulse G HTLV-I/II

The CE marked Lumipulse G HTLV-I/II immunoreaction cartridges is meant for in vitro diagnostic use with the LUMIPULSE G System for qualitative detection of antibody to HTLV-I and HTLV-II in human serum or plasma for screening of HTLV-I/II viral infection. The assay utilizes proven CLEIA (ChemiLuminescent Enzyme ImmunoAssay) technology with results that are available in up to 35 minutes.
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Reagent
ß-Hydroxybutyrate 21 FS

The β-Hydroxybutyrate 21 FS is an FDA cleared liquid-stable, ready-to-use reagent kit for the measurement of beta-hydroxybuyrate which is an important marker to detect and monitor diabetic ketoacidosis (DKA), a serious condition in diabetes mellitus. The β-Hydroxybutyrate 21 FS can be used on common clinical analyzers, and shows improved performance and excellent stabilities.
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