Pre-Departure Lateral Flow Test: Fit-to-Fly

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    Government Requirement: Mandatory test for entry into the UK from  7th December for all travelers aged 12 and over.

    Lateral Flow (Rapid Antigen) Pre-Departure Tests, the perfect solution for physical & online retail.

    • Suitable for travel to over 40* designated countries including, UK, EU and USA
    • Approved for entry into the UK for unvaccinated arrivals**

    A pre-packaged Pre-Departure lateral flow test for retailers to stock & sell to the consumer.

    The shelf-ready solution includes everything a consumer needs for their travels:

    • Lateral Flow Device (Government approved Flowflex SARS-CoV-2 Antigen Rapid Test)
    • Passenger Locator Number (PLN)
    • QR Code for easy verification (via a UKAS accredited web portal)
    • Fit-to-Fly Certificate (upload negative result to receive a signed certificate via email)
    • Full Customer Support

    Our Confirm Testing portal registers travelers details, verify’s results, uploads GDPR-compliant customer data and issues Travel Certificates to the consumer.

    * Check latest information on which destinations accept self-administered rapid antigen lateral flow tests for entry.
    ** Additional Day 2 and Day 8 PCR tests also currently required after arrival for unvaccinated travelers.

    We’re actively seeking partners for retail growth, so for more information call the team on 0114 221 3344, or email



    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.

    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!

    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.

    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.

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

    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!

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

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      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.

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