AccuPower® RV Kit (ExiStation™ FA 96)

AccuPower® RV Kit(ExiStation™ FA 96) is an in vitro diagnostic kit designed for the qualitative detection and differentiation of SARS-CoV-2, Influenza A, Influenza B, and RSV A/B.

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Cat. No.
RVP-3116

AccuPower® RV Kit (ExiStation™ FA 96) is a multiplex Real-Time PCR solution designed for the simultaneous or single qualitative detection and differentiation of SARS-CoV-2, Influenza A, Influenza B, and RSV A/B. Used with the Automated ExiStation™ FA 96, it streamlines the workflow from nucleic acid extraction to amplification for enhanced laboratory efficiency. As these respiratory viruses can present with similar clinical symptoms, accurate differential detection is essential for timely diagnosis and appropriate patient management. The assay delivers reliable molecular testing performance using human nasopharyngeal swab specimens. It is intended for use by healthcare professionals in clinical laboratory environments.  

Features and Benefits

    1. Broad detection coverage
      Detects over 40 Omicron subvariants and major influenza subtypes and lineages, including Influenza A H1N1, H3N2, Influenza B Yamagata, and Influenza B Victoria, with high sensitivity.
    2. Enhanced Convenience & Stability
      Ready-to-use premixed kit with extended shelf life, enabling room temperature shipping
    3. High sensitivity and specificity
      Dual Hot Start technology and UDG support reliable assay performance.
    4. Compatible with ExiStation™ FA 96
      Designed for use with the fully automated sample-to-result system to reduce hands-on time and minimize user error.

    Specifications

    Specimen Type Nasopharyngeal swab
    Kit Contents RVP Premix, RVP PC, RVP NTC, Sealing Film, Quick Manual
    Instrumentation ExiStation™ FA 96 (A-2500-1) 
    Tests/Kit  96

    Performances

    AccuPower® RV Kit (ExiStation FA 96) test results for clinical samples.

    An internal Positive control is used to validate the PCR results of each specific sample.

    AccuPower® RV Kit (ExiStation™ FA 96) includes negative control and positive control to verify the validity of the experiment.

    User centric ExiStation™ FA 96 software automatically analyzes the test results based upon the Ct (threshold cycle) value.

    Clinical evaluation results of AccuPower® RV Kit (ExiStationFA 96)

    RVP_Analysis figure89

    The evaluation was conducted using 859 residual clinical specimens from Europe.

    Clinical Evaluation Results


    Ordering Information

    Cat. No. Product Description Certification
    RVP-3116 AccuPower® RV Kit (ExiStationFA 96) CE-IVDR Class B


    Related Products

    Cat. No. Instrument
    A-2500-1 ExiStation™ FA 96
    Cat. No. Nucleic Acid Extraction Kit
    K-4815 ExiStation™ FA DNA/RNA Kit(V3)

    Quality Assurance

    Bioneer is the holder of Quality Management System Certificates for the following standards.

    ISO 13485 - certificate

    Contact Us

    E-mail : sales@bioneer.com

    v0.0 / 2019-03-05

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