Adenitan

STANDARD F D-dimer FIA

STANDARD F D-dimer FIA STANDARD F D-dimer FIA performs quantitative measurement of D-dimer level in plasma and whole blood samples using fluorescence immunochromatography. Through the STANDARD F Analyzer, test results with high sensitivity and specificity can be obtained. Intended Use STANDARD F D-dimer FIA is a fluorescent immunoassay for the quantitative measurement of D-dimer level in human plasma and whole blood. This test is performed to help rule out Deep Vein Thrombosis (DVT), Pulmonary Embolism (PE), and stroke.Advantage D-dimer is a cardiac marker for the diagnosis of thrombosis pulmonary embolism Automatic strip recognition by reading the information stored in a 2D barcode Reagents can be stored at room temperature Plasma and Whole blood specimens available Specification Specimen Whole blood (Sodium citrate), Plasma (Sodium citrate) Test time 7 mins Specimen volume 10 μl Measuring range 25 – 5,000 ng/mL FEU Storage temperature 2-30℃ / 36-86℉  

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STANDARD F2400 Analyser

STANDARD F2400 Analyser STANDARD F2400 is a Fluorescent immunoassay system that uses fluorescent bead as a detector. Higher sensitivity than the existing RDTs could be provided through advanced fluorescent detection with an UV LED energy source. Intended Use STANDARD F2400 Analyzer is a next-generation fluorescent immunoassay system. It is a multi-parametric and random accessible immunoassay system providing accurate diagnostic results to your laboratory. Advantage High-throughput Shortened TAT 70T/hour Random access available Automatic discarding 10” Touch Screen

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STANDARD F200 Analyser

STANDARD F200 Analyser The STANDARD F200 Analyzer is a fluorescence immunoassay device that can perform qualitative and quantitative analyses on infections, respiratory diseases, and chronic diseases, and it supports a convenient user interface and LIS/HIS connectivity. Intended Use STANDARD F Analyzer is a next-generation fluorescent immunoassay system. It is a multi-parametric and random accessible immunoassay system providing accurate diagnostic results to your laboratory. Advantage Compact size Read-only mode for batch test 50T/hour Random access available 7” LCD Touch Screen Specification INPUT 12V/8.3A AC/DC Display 7 Display Controls Graphic User Interface Power Consumption Max 60W Memory 3000 Real Time Clock RTC Backup Battery Included LIS/HIS HL7 PCD-01 Profile Support Size 200 x 240 x 205 mm Bar Code Scanner (Option) USB Barcode Scanner weight 2.7kg

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STANDARD Transport Medium

STANDARD Transport Medium STANDARD Transport Medium is intended for the and transport of clinical specimens containing viruses, Chlamydiae, Mycoplasma or Ureaplasma from the collection site to the testing laboratory. Bacterial and fulgal flora inhibition Internal conical tube that can stand alone Available multiple tests with large volume of transport medium Stable at room temperature Intended Use Transport Medium is intended for the transportation and preservation of clinical specimens containing viruses, Chlamydiae, Mycoplasma or Ureaplasma.

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STANDARD Q COVID-19 Ag Saliva

STANDARD Q COVID-19 Ag Saliva STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigens to SARS-CoV-2 present in Saliva specimens with mucus. Test time : Within 15 mins Easy and convenient testing process for professionals Effective in detecting the SARS-CoV-2 variant Effective in detecting the SARS-CoV-2 variant No need for extra equipment Intended Use STANDARD Q COVID-19 Ag Test is a rapid chromatographic immunoassay for the qualitative detection of nucleocapsid antigens to SARS-CoV-2 present in human saliva specimens with mucus. This test is for administration by healthcare workers and labs only, as an aid to early diagnosis of SARS-CoV-2 infection in patient with clinical symptoms with SARS-CoV-2 infection. It provides only an initial screening test result. This product is strictly for medical professional use only and not intended for personal use. The administration of the test and the interpretation of the results should be done by a trained health professional. The result of this test should not be the sole basis for the diagnosis; confirmatory testing is required.

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