Influenza A+B Rapid Test – Product code: SC-0623-20 Rapid test for the qualitative detection of the Influenza A and Influenza B virus on samples of nasal swab, throat swab or nasal aspirate. The Influenza A + B rapid test is a rapid immunochromatographic test for the qualitative identification of influenza A and B antigens on nasal, pharyngeal or nasal aspirate swab samples. It is intended to assist in the rapid differential diagnosis of viral infections of influenza A and B. Influenza is an acute, highly contagious viral infection of the respiratory tract. It is a highly transmissible contagious disease through coughing and sneezing from suspended droplets containing the live virus. The peak of the flu usually occurs during the winter and autumn months each year. Type A viruses are usually more prevalent than type B and associated with more serious influenza outbreaks, while type B infections are usually milder.
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Sars-Cov-2 Antigen + Flu A/B Rapid Test – Codice Prodotto: SC-1262-20 The Covid-19 Antigen Rapid Swab and Influenza A + B (nasopharyngeal swab) is a rapid immunochromatographic test for the qualitative detection of the antigens of the Sars-CoV-2, Influenza A and Influenza B viruses present in the human nasopharynx. For professional in vitro diagnostic use only. The separate results indicate the detection of Sars-CoV-2 and Influenza A + B antigens. The antigen is generally detectable in upper respiratory tract samples during the acute phase of the infection. Positive results indicate the presence of viral antigens, but a clinical correlation with the patient’s medical history and other diagnostic information is required to determine the infectious state. The positive results do not exclude bacterial infection or co-infections with other viruses.
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The Clostridium difficile Toxin A + Toxin B combination rapid test (Feces) is a rapid chromatographic immunoassay for the qualitative detection of Toxin A and Toxin B Clostridium difficile antigens in human stool samples. The Clostridium difficile Toxin A + Toxin B Combination Rapid Test detects two distinct antigens in stool samples for C. difficile, viz., Toxin A and Toxin B on two different test strips in the same device, thus simultaneously detects two specific Clostridium antigens hard. Clostridium difficile is an anaerobic bacterium that acts as an opportunistic pathogen: it grows in the intestine when the normal flora is altered by antibiotic therapy. Toxigenic strains of Clostridium difficile cause infections from simple diarrhea to pseudomembranous colitis, which can even cause death. The disease is caused by two toxins produced by the toxigenic strains of C. difficile:
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Rapid test for the qualitative detection of Helicobacter pylori (H.pylori) antigens in human feces. For professional in vitro diagnostic use only. The rapid test for H. pylori antigen (Feces) is a chromatographic immunoassay for the qualitative identification of H. pylori antigens. pylori in stools to aid in the diagnosis of H. pylori infection. The H. pylori is a small coiled bacterium that lives on the surface of the stomach and duodenum. It is involved in the etiology of various gastrointestinal disorders, including duodenal and gastric ulcers, non-ulcer dyspepsia and acute and chronic gastritis. Both invasive and non-invasive methods are used to diagnose H. pylori infection in patients with symptoms of gastrointestinal diseases. Sample and costly invasive diagnostic methods include gastric or duodenal biopsy followed by urease test (presumable), culture and / or histological section.
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Disposable screening rapid test to simultaneously detect creatinine, nitrites, glutaraldehyde, pH, specific weight and oxidants/pyrhythinium chlorren in human urban. The disposable test of the sample is a semi-quantitative screening test that is based on color comparison, to detect creatinine, nitrites, glutaraldehyde, pH, specific weight and oxidizing/pyrhythin chrook (CCP) in human urine. This test provides only a preliminary screening. To achieve certain analytical results, you need to use a more specific alternative chemical method. Abnormal results should be sent to the laboratory for confirmation. Each plastic strip contains six (6) Reagent chemical pads. After a (1) minute from the activation of reagent pads with the urine sample, it is possible to compare the colors that appear on the pads with the scale of the colors shown on the bottle.
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