220 Compañías | 938 productos médicos

SARS-CoV-2 Test
SARS-CoV-2 Nucleic Acid Detection Kit

The TianLong SARS-CoV-2 Nucleic Acid Detection Kit is intended for the qualitative detection of SARS-Cov-2 nucleic acid by Real-time reverse transcription Polymerase Chain Reaction (Real-time RT-PCR) method.
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CONTROLES PARA SARS-COV-2
Qnostics SARS-CoV-2 Typing

Qnostics SARS-CoV-2 Typing son controles reactivos y no reactivos destinados a usarse con ensayos in vitro para la determinación de anticuerpos de spike contra el SARS-CoV-2. Estos controles se pueden utilizar en varios analizadores.
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COVID-19 Antigen Self-Test
Panbio COVID-19 Antigen Self-Test

The Panbio COVID-19 Ag Rapid Test Device can identify potentially COVID-19 contagious people with or without symptoms in 15 minutes. The test can be deployed in a wide variety of settings and provides fast, accurate and reliable results to help protect your loved ones and the vulnerable. Panbio COVID-19 tests are used by healthcare professionals in over 100 countries but are not available in all countries and available to consumers in select markets.
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COVID-19, Flu A/B Multiplex RT-PCRTest
TaqPath COVID-19, FluA, FluB Combo Kit

The TaqPath COVID-19, FluA, FluB Combo Kit is a multiplex real-time RT-PCR test intended for the simultaneous qualitative detection and differentiation of RNA from the SARS-CoV-2, influenza A, and/or influenza B viruses in nasopharyngeal swab and anterior nasal swab specimens collected from individuals suspected of respiratory viral infection consistent with COVID-19 by their healthcare provider. The kit is authorized for use on the Applied Biosystems 7500 Fast Dx Real-Time PCR and QuantStudio 5 Real-Time PCR System (96-well, 0.2 mL block) with nasopharyngeal swab and anterior nasal swab specimens only.
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SARS‑CoV‑2 Sample-To-Answer Test
SARS‑CoV‑2 Cartridge (CE-IVD)

The SARS‑CoV‑2 Cartridge (CE-IVD) is a sample-to-answer COVID-19 testing cartridge that enables quick and easy testing anywhere on the FLASH Dx multiplexed molecular point of care diagnostic system. The one-hour sample-to-answer test is designed to detect three genes (N gene, E gene and ORF1ab gene) of the SARS‑CoV‑2 virus from nasopharyngeal, nasal and throat swab samples.
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SARS-CoV-2 Antibody Test
iFlash-SARS-CoV-2 IgM/IgG Antibody Test

The iFlash-SARS-CoV-2 IgM/IgG Antibody Test provides a comprehensive solution for the detection of COVID-19 with reagent kits for both IgG and IgM tests for SARS-CoV-2. Speed: Up to 1200 T/H can be achieved on the company’s iFlash series CLIA analyzers (iFLash 1800: 180 T/H; iFlash 3000: 300 T/H, iModule: up to 1200 T/H).
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SARS-CoV-2 RT PCR Kit
SARS-CoV-2 Variant Lambda (C.37) Real Time PCR Kit (RUO)

SARS-CoV-2 Variant Lambda (C.37) Real Time PCR Kit (RUO) helps to identify the Lambda variant by targeting ORF1a/b, F490S and T76I. The results can be interpreted quickly and conveniently by an automatic result interpretation tool.
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SARS-CoV-2 Assay
INgezim COVID RBD-DR

INgezim COVID RBD-DR is a CE-marked double recognition enzyme-linked immunosorbent assay for detecting antibodies specific to S (RBD) of SARS-CoV-2 in human serum samples. The highly sensitive test is particularly recommended for the early detection of SARS-CoV-2 specific antibodies as it favors the detection of IgM.
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PRUEBA RÁPIDA DE ANTÍGENO SARS-COV-2
RapiSafe SARS-CoV-2 Antigen Rapid Test (Colloidal Gold)

La prueba rápida de antígeno SARS-CoV-2 RapiSafe (oro coloidal) está diseñada para la detección temprana del antígeno específico del SARS-CoV-2 de casos sospechosos de COVID-19. Ofrece resultados en 15 minutos sin instrumentos adicionales.
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MEDIO DE TRANSPORTE
TRANSPORT MEDIUM-2

El MEDIO DE TRANSPORTE-2 de Vircell está diseñado para la recolección y conservación de las muestras de saliva con SARS-CoV-2 e influenza A. Se suministra en tubos etiquetados con tapón de rosca, diseñados para conservar y transportar la muestra clínica.
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COVID-19 Antigen Test
Panbio COVID-19 Ag Rapid Test Device

The Panbio COVID-19 Ag Rapid Test Device is intended for patients suspected of current COVID-19 infection and identifies potentially contagious patients in 15 minutes. Using patient-friendly nasal or nasopharyngeal sample collection types, the high performance rapid test enables immediate treatment or isolation measures to minimize transmission. The product is not available in all countries and available in select markets.
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SARS-CoV-2 Multiplex Real-Time RT-PCR Test
STANDARD M10 SARS-CoV-2

The STANDARD M10 SARS-CoV-2 is a multiplex real-time RT-PCR test intended for use with STANDARD M10 system for the qualitative detection of nucleic acid from the SARS-CoV-2 in upper respiratory specimens (such as nasopharyngeal) collected from individuals suspected of COVID-19. Reverse transcription real-time polymerase chain reaction (Real-time RT-PCR) is used for amplification and detection of SARS-CoV-2.
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SARS-CoV-2/Influenza A, B and RSV Test
REALQUALITY ResP-Aria

REALQUALITY ResP-Aria is a kit for the identification of respiratory viruses SARS-CoV-2, Influenza A, Influenza B and RSV and their timely differential diagnosis, allowing for early therapeutic treatment and at the same time limiting the spread of COVID-19. The automatic format of the REALQUALITY ResP-Aria kit, especially for high throughputs, is supported by the GENEQUALITY X120 automatic platform, version with 96 extractions and PCR plate set-up.
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SARS-CoV-2 Saliva PCR System
SARS-CoV-2 Saliva PCR System

MicroGEM’s SARS-CoV-2 Saliva PCR System combines the Sal6830 Point of Care PCR System (U.S.) and Sal6830 SARS-CoV-2 Saliva Testing System (Canada) with the Sal6830 saliva test to detect SARS-CoV-2 at the POC in under 30 minutes.
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SARS-CoV-2 Saliva Test
Sal6830 SARS-CoV-2 Saliva Test

MicroGEM’s Sal6830 SARS-CoV-2 Saliva Test (U.S.) and Sal6830 SARS-CoV-2 Saliva Testing Kit (Canada) (hereafter Sal6830 saliva test) is the first-of-a-kind PCR-based saliva test for fast, simple, on-the-spot detection of COVID-19 infection not possible until now. The innovative design of the Sal6830 SARS-CoV-2 saliva test targets both the E and N genes on SARS-CoV-2, reducing the risk of current and future variants affecting the efficacy of the test.
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