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Rapid Tests
251 Compañías | 1397 productos médicos

COVID-19 Antigen Test
ezLabs COVID-19 Antigen Test

The ezLabs COVID-19 Antigen Test is a rapid in-vitro immunochromatographic assay for the qualitative detection of SARS-CoV-2 virus antigen present in human nasopharynx.
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PT/INR Monitoring System
qLabs PT/INR Monitoring System

The qLabs PT/INR test is an easy-to-use finger-stick blood test, designed for professional or home use, that provides highly accurate results within 2 minutes. The dry reagent strips can be stored at room temperature for immediate use for up to 18 months, with no equilibration required. qLabs PT/INR test is CE marked and distributed outside of the US.
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Diagnostic Test Card
Fluxergy Test Card

Fluxergy Test Card is a single-use, highly integrated consumable, allowing for rapid PCR results and simplifying tedious traditional workflows. Designed for fast sample-to-answer testing, Fluxergy’s test cards are manufactured for high-volume scalability, using printed circuit board manufacturing technologies to reach millions of people.
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COVID-19 RT-PCR Test
Fluxergy Test Kit COVID-19

Fluxergy Test Kit COVID-19 is a real-time reverse transcriptase (rRT) polymerase chain reaction (PCR) test intended for the qualitative detection of nucleic acid from SARS-CoV-2 in nasopharyngeal swab samples (NPS). The assay consists of one Fluxergy Reaction Mix COVID-19 and one Fluxergy Card. The assay is performed on the Fluxergy Analyzer instrument which is controlled by an external computer equipped with Fluxergy Works Software.
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COVID-19 Test & PCR Analyzer
Fluxergy Analyzer and Test Kit COVID-19 CE

Fluxergy Analyzer and Test Kit COVID-19 CE consists of the Fluxergy Analyzer that is designed to deliver test results within one hour and the Fluxergy Test Kit COVID-19, which utilizes state-of-the-art PCR and microfluidics technology to identify the SARS-CoV-2 virus. Fluxergy’s simple workflow on a compact analyzer along with the assay targeting the SARS-CoV-2 N-gene and orf1ab gene v make it ideal for use in laboratory or field settings.
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Patient Portal App
KAYA17's Patient Results Portal

The KAYA17 patient portal app has two functions. It helps make patient registration fast, seamless and contactless. Patients can enter their profile information before coming for a COVID-19 test. The second function of the app is to display the results of a test. After the test is completed, the patient does not have to wait for their results at the test site. Results will be automatically sent to their phone. The patient portal app is available in both iOS and android platforms.
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Results Manager
KAYA17's Results Manager

KAYA17’s system allows parallel COVID-19 testing with multiple readers. One patient ID computer can be connected to 10 readers operating in parallel. The results from all of the readers are transmitted to the patient ID computer where a report is generated for each patient. Results of the test can be printed as a patient test report, sent to their phone, or synched up with a central hospital or healthcare database.
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Vertical Flow Cartridge (VFC)
KAYA17's Cartridge System

KAYA17 has designed a proprietary one-time use Vertical Flow Cartridge (VFC) on which the COVID-19 test sample is processed, keeping the reader free during this time. The cartridge is inserted into an electronic reader for one minute. The patient ID QR code label is placed on the cartridge to ensure that the sample can be traced at all times.
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Patient Registration Software
KAYA17's Patient ID Software

KAYA17 has designed a patient registration software that gathers patient information and generates a unique patient QR code that is applied to their sample tube and cartridge used to process their COVID-19 test sample. The software can also receive this information from a QR code from a patient portal app.
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IgG/IgF IVD Test
ImmuneCheck IgG/IgF

The ImmuneCheck IgG/IgF is an in vitro diagnostic test intended for the real-time monitoring of human IgG content based on immunochromatography technique. It is the world’s first direct whole blood test kit for total IgG concentration measurement and delivers results in 20 minutes without any instrument using 5 ul of blood sample.
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COVID-19 IgG/IgM Assay
KOVIcheck COVID-19 IgG/IgM

The KOVIcheck COVID-19 IgG/IgM is an immunochromatographic assay for the detection of SARS-CoV-2 specific human Immunoglobulin G and Immunoglobulin M. The rapid test detects SARS-CoV-2 antibodies within 15 minutes in whole blood, serum or plasma samples.
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COVID-19 IVD Kit
GENEdania COVID-19 qRT-PCR Kit

GENEdania COVID-19 qRT-PCR Kit is an in-vitro diagnostic kit for qualitative detection of SARS-CoV-2 RNA extracted from human Nasopharyngeal swab, Oropharyngeal swab and sputum using real-time RT-PCR (Reverse Transcription-Polymerase Chain Reaction). It detects three gene regions simultaneously (Orf1ab gene, N gene, E gene) using one tube by one step real-time PCR assay.
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SARS-CoV-2 Antigen Test
RIDAQUICK SARS-CoV-2 Antigen

The RIDAQUICK SARS-CoV-2 Antigen is a manual immunochromatographic rapid detection test for the qualitative detection of SARS-CoV-2-specific antigens in human respiratory samples from persons with a reasonable suspicion and/or symptoms of SARS-CoV-2 infection as well as from asymptomatic persons. The test is a diagnostic aid to detect and/or rule out a respiratory tract infection with SARS-CoV-2 in connection with other clinical and laboratory findings.
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Cancer Panel
ONCOaccuPanel

ONCOaccuPanel is a comprehensive cancer panel capable of identifying immunotherapy biomarkers TMB (tumor mutational burden) and MSI (Microsatellite Instability) using next-generation sequencing (NGS). The panel targets the 323 genes (225 genes with entire coding exon, 98 genes with partial exon/hot spots) associated with solid tumors. The NGS data produced with ONCOaccuPanel can be analyzed with the automated analysis software NGeneAnalySys, which enables identification of all DNA variants (SNVs, INDELs, CNV, SV, translocation).
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Hematologic Malignancy Test
HEMEaccuTest

HEMEaccuTest is intended for molecular genetic test of multiple genes related hematologic malignancy using the next generation sequencing (NGS) method. Its purpose is to assist in appropriate classification and prediction of prognosis.
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