Flowflex Influenza A/B Rapid Test – Single Pack

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    Description

    The Flowflex Influenza A/B Rapid Test is a market leading self-test for the detection of Influenza virus type A, including the present have-known subtypes, and type B antigens directly from nasal specimens from individuals who have the onset of symptoms.

    The CE marked self-test is suitable for home and professional use.

    • CE certified for use in the UK & EU
    • Accuracy: 99.38% (97.63%-99.98%)
    • Sensitivity: 100% (93.60%-100%)
    • Specificity: 99.22% (97.01%-99.97%)
    • Convenient anterior nasal swab specimens
    • Fast Results in 15 minutes
    • Room temperature storage

    Kit contents:

    • 1 Test Cassette
    • 1 Sterile Short Nasal Swab
    • 1 Pre-filled Extraction Buffer Tube
    • 1 Waste Bag
    • 1 Instructions

    Flowflex test kits are CE certified for professional use and as a self test.

    View the Product Data Sheet

    Additional information

    Pack quantity

    1
    Case quantity

    300

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    A vast range of PPE products at competitive prices, but crucially the expertise behind the products and the quality of them is second to none.

    — Pay Broadbent

    A great company to deal with, extremely reliable with a good range of products. Excellent product knowledge, great communication & customer service, fair prices and fast delivery.

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    Hygiene UK is great business providing essential supplies to essential services.

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    Huge range of products at great prices. At a time of desperate need many were taking advantage of people, but not Hygiene UK. They have helped us and have been nothing but perfect. If you’re looking for masks, gloves, aprons, etc please give the team at Hygiene UK a call!

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    — Seldram Supplies

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      An IVD Medical Device is defined in the IVDR as “any medical device which is a reagent, reagent product, calibrator, control material, kit, instrument, apparatus, piece of equipment, software or system, whether used alone or in combination, intended by the manufacturer to be used in vitro for the examination of specimens derived from the human body.

      In vitro diagnostics (IVDs) are tests that can detect disease, conditions and infections. In vitro simply means 'in glass', meaning these tests are typically conducted in test tubes, cassettes and similar equipment, as opposed to in vivo tests, which are conducted in the body itself.

      The IVDR is the new regulatory basis for placing on the market, making available and putting into service in vitro diagnostic medical devices on the European market. It will replace the EU’s current Directive on in vitro diagnostic medical devices (98/79/EC). As a European regulation, it will be effective in all EU member states and EFTA states immediately without need to be transferred into the law of respective states, however national laws may be adapted to back up some requirements in more detail.

      The IVDR came into force on 25 May 2017. Several implementing acts/guidance documents are being issued by the EU commission and are stipulated to complete some of the requirements to be met.

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