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250 Compañías | 1369 productos médicos

Point-of-Care Coronavirus Antigen Test
New Antigen Test (NAT)

Kaya17’s New Antigen Test (NAT) for point-of-care SARS-CoV-2 testing gives 98% accurate results with PCR-level sensitivity in 15 minutes, using saliva at less than half the cost of PCR with a free USB-powered reader. The reader processes 30-60 samples/hour and the product has CE-IVD certification.
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Free Mobile Application
MYACUTECASE

MYACUTECASE is a free mobile application by bioMérieux to support clinicians in decision-making and monitoring of patients using emergency and critical care diagnostics. The first of a kind mobile application serves as an aid in the interpretation of VIDAS emergency and critical care biomarker tests. The first version of bioMérieux’s easy-to-use mobile application addresses four emergency and critical care assays, namely VIDAS D-Dimer Exclusion II, VIDAS NT-proBNP2, VIDAS B.R.A.H.M.S PCT, and VIDAS High sensitive Troponin I.
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Acute Coronary Syndrome Panel
VIDAS Acute Coronary Syndrome Panel

The VIDAS Acute Coronary Syndrome (ACS) panel offers three complementary tests for the assessment of myocardial injury - VIDAS Troponin I Ultra, VIDAS CK-MB and VIDAS Myoglobin. Performed on the instruments of the VIDAS family, these assays are particularly suitable for emergency testing for the assessment of myocardial damage.
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PRUEBA DE LESIÓN RENAL AGUDA
NEPHROCHECK

NEPHROCHECK es una prueba innovadora que detecta el estrés renal antes del daño real, cuando la intervención aún puede marcar la diferencia. Está destinado a ser utilizado como una prueba de evaluación de riesgos, junto con la evaluación clínica.
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Hepatitis B Surface Antigen Test
HBsAg (Hepatitis B Surface Antigen) Test Kit (ELISA)

The HBsAg (Hepatitis B Surface Antigen) Test Kit (ELISA) is a qualitative test for the detection of HBsAg. The reagent is suitable for clinical screening and diagnosis of hepatitis B virus infection in human serum/plasma.
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Sepsis Risk Stratification Test
IntelliSep

IntelliSep is a simple and novel test for sepsis diagnosis that provides results in less than 10 minutes. The sepsis risk stratification test is designed to quantify the state of immune activation by measuring the biophysical properties of leukocytes from a routine blood sample.
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Respiratory Multiplex Real-Time PCR Diagnostic Kit
Multiplex Real-Time PCR Diagnostic Kit for Rapid Detection of 6 Respiratory Viruses

The XABT multiplex real-time PCR diagnostic kit for the rapid detection of six respiratory viruses offers a more reliable diagnosis method for pathogen and can detect six targets in two tubes. The four-channel RT-PCR instrument can detect the Influenza A Virus, Influenza B Virus, Respiratory Syncytial Virus (RSV), Adenovirus (ADV), Parainfluenza Virus Type I (PIVI) and Parainfluenza Virus Type III (PIVIII), and has a one hour post-extraction turnaround time.
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Respiratory Pathogen Antigen Rapid Test
Respiratory Pathogen Antigen Rapid Test Cassette (Colloidal Gold Method)

The XABT respiratory pathogen antigen rapid test cassette (Colloidal Gold Method) detects six respiratory pathogens including Flu A/Flu B/RSV/ADV/MP/2019-nCoV Ag from oropharyngeal and nasopharyngeal swab samples.
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Influenza Virus & 2019-nCoV Test
Influenza Virus & 2019-nCoV-Combined Nucleic Acid Testing Protocol

The XABT Influenza Virus & 2019-nCoV-Combined Nucleic Acid Testing Protocol enables the convenient, efficient and rapid detection of three pathogens - Influenza Virus A, Influenza Virus B and 2019-nCoV - with three tubes simultaneously. It enables differential diagnosis between the influenza virus and 2019-nCoV determination by triple targets, and comes with sensitive and precise internal control.
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2019-nCoV Antigen Rapid Test Cassette
2019-nCoV Antigen Rapid Test Cassette

The XABT 2019-nCoV Antigen Rapid Test Cassette is a lateral flow immunoassay intended for the qualitative detection 2019-nCoV nucleocapsid antigens in nasopharyngeal swab and oropharyngeal swab from individuals who are suspected of 2019-nCoV infection by their healthcare provider. The test is CE marked.
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2019-nCoV Rapid Antibody Test
2019-nCoV Neutralization Antibody Rapid Test Cassette (Fluorescence immunochromatography)

The XABT 2019-nCoV Neutralization Antibody Rapid Test Cassette (Fluorescence immunochromatography) is a lateral flow immunoassay intended for the qualitative detection 2019-nCoV neutralization antibody in serum, plasma and whole blood. Using purified receptor binding domain (RBD), protein from the viral spike (S) protein and the host cell receptor ACE2, the test is designed to mimic the virus-host interaction by direct protein-protein interaction. The highly specific interaction can then be neutralized.
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2019-nCoV Antibody Rapid Test
2019-nCoV Neutralization Antibody Rapid Test Cassette (Colloidal Gold Method)

The XABT 2019-nCoV Neutralization Antibody Rapid Test Cassette (Colloidal Gold Method) is intended for the qualitative detection 2019-nCoV neutralization antibody in serum, plasma and whole blood.
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AUTOPRUEBA RÁPIDA DE ANTÍGENO 2019-NCOV
2019-nCoV Antigen Rapid Test Cassette (Self)

El casete de prueba rápida de antígeno XABT 2019-nCoV es un inmunoensayo de flujo lateral destinado a la detección cualitativa de antígenos de la nucleocápside del SARS-CoV-2 en un hisopo nasal anterior.
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2019-nCoV RT-PCR test
Multiple Real-Time PCR Kit for Detection of 2019-nCoV

The XABT Multiple Real-Time PCR Kit for Detection of 2019-nCoV is a Real-Time RT-PCR test intended for the qualitative detection of nucleic acid from the 2019-nCoV in oropharyngeal swabs, nasopharyngeal swabs and sputum from individuals with signs and symptoms of infection who are suspected of COVID-19. The kit has WHO EUL (Emergency Use Listing) and is to be used only for IVD emergency capacity for 2019-nCoV and auxiliary diagnosis of related cases with Novel Coronavirus infections, which cannot be used as a routine IVD in clinic.
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SARS-CoV-2 IgG ELISA Test
SARS-CoV-2 IgG ELISA Kit

The SARS-CoV-2 IgG Enzyme-Linked Immunosorbent Assay (ELISA) kit intended for the qualitative detection of immunoglobulin G (IgG) antibodies to SARS-CoV-2 in human serum or plasma. The qualitative two-step indirect ELISA for the detection of human IgG antibodies to the SARS-CoV-2 S1 RBD protein is intended for use as an aid in identifying individuals with an adaptive immune response to SARS-CoV-2, indicating recent or prior infection.
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