Standard M10

Standard M10 Flu/RSV/SAR-CoV-2

Standard m10 Flu/RSV/SARS-CoV-2 TANDARD M10 Flu/RSV/SARS-CoV-2 is a molecular in vitro diagnostic assay that aids in the simultaneous detection and identification of Influenza A, Influenza B, RSV, and SARS-CoV-2 viral RNA based on nucleic acid amplification technology, real-time RT-PCR. STANDARD M10 Flu/RSV/SARS-CoV-2 is an all-in-one cartridge containing nucleic acid extraction and amplification reagents, which simplifies the testing process and allows users to obtain results within 1 hour. Intended Use STANDARD M10 Flu/RSV/SARS-CoV-2 is a multiplex real-time RT-PCR test intended for use with STANDARD M10 system for the qualitative detection of Influenza A, Influenza B, RSV and SARS-CoV-2 nucleic acids in human nasopharyngeal swab specimen. Advantage All-in-one cartridge (NA extraction + amplification) Simultaneous detection and identification of Flu A, Flu B, RSV and SARS-CoV-2 Real-time RT-PCR result in 1 hour One minute hands-on preparation Room temperature storage Specification Test method Real-Time RT-PCR Detection or analysis of gene Influenza A, Influenza B, RSV, ORF1ab gene, N gene Specimen type Nasopharyngeal swab (VTM/UTM) 300μl Limit of detection Influenza virus: Flu A H1N1 pdm (399 copies/mL), Flu A H1 (631 copies/mL), Flu A H3 (525 copies/mL), Flu B (399 copies/mL) RSV: RSV A (795 copies/mL), RSV B (2,631 copies/mL) / SARS-CoV-2: ORF1ab gene (813 copies/mL), N gene (795 copies/mL) Sensitivity Influenza A: 98.18% (108/110) [95% CI: 93.59% – 99.78%], Influenza B: 98.91% (91/92) [95% CI: 94.09% – 99.97%], RSV: 98.78% (81/82) [95% CI: 93.39% – 99.97%], SARS-CoV-2: 96.49% (165/171) [95% CI: 96.69% – 99.98%] Specificity Influenza A: 100.00% (535/535) [95% CI: 99.31% – 100.00%], Influenza B: 99.82% (552/553) [95% CI: 99.00% – 100.00%], RSV: 100.00% (563/563) [95% CI: 99.35% – 100.00%], SARS-CoV-2: 98.73% (468/474) [95% CI: 97.72% – 99.53%] Test time 60 minutes Storage temperature 2 ~ 28℃ Test/Kit 10 Tests

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Standard M10 MDR-TB

Standard M10 MDR-TB STANDARD M10 MDR-TB is a molecular in vitro diagnostic assay that aids in the simultaneous detection of Mycobacterium tuberculosis complex and drug-resistance against rifampicin (RIF) and isoniazid (INH) based on nucleic acid amplification technology, real-time PCR. STANDARD M10 MDR-TB is an all-in-one cartridge containing nucleic acid extraction and amplification reagents, which simplifies the testing process and allows users to obtain results within 86 minutes. Intended use STANDARD M10 MDR-TB is a multiplex real-time PCR test intended for use with STANDARD M10 system for the qualitative detection of Mycobacterium tuberculosis complex nucleic acids and drug-resistance against rifampicin (RIF) and isoniazid (INH) in human normal sputum or sputum sediment sample. Advantage All-in-one cartridge (NA extraction + amplification) Simultaneous detection of M. tuberculosis complex and drug-resistance against rifampicin (RIF) and isoniazid (INH) Fast result in 86 minutes Room temperature storage

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Standard M10 SARS-CoV- 2

Standard M10 SARS-CoV- 2 STANDARD™ M10 is an automated point of care MDx system. STANDARD M10 is a random access and scalable solution that enables simple, fast and accurate molecular diagnostic of infectious disease, drug resistance and genetic testing from human specimens. The Standard M10 POC MDx is a versatile system that uses the Loop Mediated Isothermal Amplification (LAMP) and the Real Time Polymerase Chain Reaction (RT-PCR) process for the diagnosis of Viral Infections. The LAMP module of the Standard M10 offers an easier to operate, multiplex DNA analysis, fully enclosed system which reduces risk of sample contamination than the PCR. Yet, in keeping with the gold standard for viral evaluation, the RT-PCR option is also available on the Standard M10. The standard M10 also offers various menu assays for Tuberculosis, HIV and Hepatitis, SARS COV-2 among others. The standard M10 is CE certified and certification by the FDA EUA is currently in progress. Amongst others, the standard M10 offers the following benefits: An intuitive result interpretation Detailed summary per test Colored index indicating positive/negative/invalid. Amplification curve displayed per test. Accurate data analysis algorithm Memory up to 10,000 Fast result Isothermal amp result in 20-30 minutes RT-PCR result in 45-60 minutes Application of optimized method Qualitative assay (lamp) Qualitative assay (RT-PCR) Viral load assay (RT-PCR) Point mutation detection. Randomly accessible analyzer Minimized maintenance requirements. Intuitive status indicator Small footprint (14cm x 33cm x 32cm) Seamless connectivity 1” touchscreen Scalable configuration setting A larger number of tests are carried out per time. Multiplex assay; up to 11 targets fam/hex/cy5 One cartridge contains 4 wells and 3 fluorescent dyes for 11 targets

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