AllTest SARS-CoV2 and Influenza A+B Antigen Combo Rapid Test

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    Description

    The AllTest SARS-CoV-2 and Influenza A+B Antigen Combo Rapid Test is a self-test for the combined detection of SARS-CoV-2 (Covid 19), and Influenza.

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

    • CE certified for home use in the UK & EU
    • UK MHRA registered
    • Accuracy:
      • SARS-CoV-2: 98.92%
      • Flu A: 99.1%
      • Flu B: 98.92%
    • Sensitivity:
      • SARS-CoV-2: 96.99%
      • Flu A: 95.77%
      • Flu B: 94.12%
    • Specificity:
      • SARS-CoV-2: 99.59%
      • Flu A: 99.59%
      • Flu B: 99.41%
    • Convenient nasal swab specimens
    • Fast Results in 10 minutes
    • Room temperature storage

    Kit contents:

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

    Additional information

    Pack quantity

    1
    Case quantity

    400

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    Testimonials

    We first ordered products from Hygiene UK at the start of the pandemic as our usual suppliers could not supply, and had increased their prices drastically. We were offered competitively priced and good quality PPE at a time when not many suppliers could. You delivered timely deliveries to all of my locations, and your team are always friendly and helpful. I will continue to work with you when required.

    — Primera Healthcare

    Great products and pricing, and the team are always helpful and friendly.

    — Natura Clean

    We've used Hygiene UK many times and have nothing but good things to say. Great Prices, reliable & quick delivery. We use Hygiene UK to supply our blue-chip clients so confidence is a must! Thoroughly recommend!

    — Plane Talking

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

    — Broadbent Welding and Industrial Supplies

    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.

    — Jackson Handling

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

    — Hope City Foundation

    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!

    — Global Office Supplies

    Pleasure to deal with, great communication and overall service levels. Highly recommended.

    — Seldram Supplies

    Pleasure to deal with Hygiene UK Ltd, quick service and always available to answer questions.

    — Whitworth Pharmacy
    —

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      FAQs

      Find what you might need in our FAQ's...

      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.

      All the usual methods of communication can be used, phone, email, and the contact form on the website. Whichever method suits your needs best, check out the website footer for our contact information. Additionally if you need a face to face meeting we are more than happy to come visit.

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