Official distributors of HeiQ's revolutionary anti-microbial technology.
VIRA-X the unique HeiQ Viroblock Hygenizer is suitable for a range of surface types. The most suitable in today’s environment range from the following:
Face masks, PPE gowns, work uniforms, bedding, curtains, soft furnishings, carpets, tables, car seats, travel, all personal clothing, shoes plus numerous accessories.
End user applications include:
All Healthcare workers, social care workers, public transport workers, school teachers and support staff, delivery drivers, factory and warehouse workers, key retail operatives, council staff, not forgetting the home and personal care.
Treating your own clothes and accessories such as bags/ handbags etc, will help protect you travelling to and from work.
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HeiQ Viroblock is effective in significantly reduces bacterial, fungal and viral infection. Icluding Novel Coronavirus, MRSA, Parvlovirus, Candida Auris & Norovirus. Improving the personal safety of the wearer and those in close contact. Reducing the opportunity for live transmission of the virus from one garment to another or to any other surface.
By simply applying VIRA-X to your clothes, shoes, car seats etc will reduce the incidence of COVID19 transmission from place to place, and person to person, keeping your workplace and home safer with VIRA-X than without.
VIRA-X is effective in minutes, but with just one application can keep protecting you for weeks afterwards.
99.99% REDUCTION OF THE COVID-19 CAUSING VIRUS
HeiQ Viroblock is among the first textile technologies in the world to be proven effective against SARS-CoV-2 by an independent institution*. SARS-CoV-2 is an enveloped virus from the coronavirus family that causes COVID-19. Tests have been conducted by HeiQ with the Peter Doherty Institute for Infection and Immunity in Melbourne, Australia (Doherty Institute). HeiQ Viroblock is designed to inhibit the growth and persistence of bacteria and enveloped viruses on textile surfaces. It’s a unique combination of our registered silver technology for antiviral and antibacterial effect and our vesicle technology as a booster. * M.J. (2020) Report on “Viral Stability and Persistence of SARS-CoV-2 on Treated Material”. Doherty Institute for Infection and Immunity, Melbourne.
99.99% REDUCTION OF THE COVID-19 CAUSING VIRUS
*subject to availability.* CONTACT US
HeiQ Viroblock Hygenizer treated nonwoven material shows excellent antiviral efficacy.
Aerosol challenge test ASTM F2101(7): Face masks (N95/FFP2/KN95 type) treated with HeiQ Viroblock (Viroblock) have been tested according to GLP standards relative to the untreated control masks.(8) Treated face masks show significantly improved reduction in virus infectivity compared to untreated control masks.(9)
Antiviral efficacy test (ISO 18184): Nonwoven material for disposable face masks treated with HeiQ Viroblock has been tested according to ISO 18184 standard.(10) HeiQ Viroblock treated nonwoven material shows excellent antiviral efficacy.
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(7) Test performed according to Aerosol challenge test (ASTM F2101) with modifications to virus testing.
(8) 2013, ID number 798110-798116, Microbac Laboratories Inc. USA, Dr. Zhou. ASTM F2101 is NOT a simple antimicrobial test!The test mask is mounted and sealed within a test chamber. A nebulizer delivers an aerosol of the target virus inoculum to the upstream side of the mask. A collection dish placed below the mask downstream collects aerosol droplets that pass through the mask sample. The reduction in infectivity with and without mask is calculated as an indicator of effectiveness.
(9) Difference in log reduction of Δ=1 indicates 10x and Δ=2 indicates 100x
(10) 2020, 2020FM 03839R06 test report, “ISO 18184 – Determination of antiviral activity of textile products”, Guandong Detection Center of Microbiology, China
See published test reports
Data source courtesy of : http://www.finder.com/uk/mask-usage
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DISCLAIMER: Active healthcare claims on treated articles such as antiviral are not permitted in the USA and require pesticidal device registration. Antiviral claims are permitted in Germany on most treated articles and can be evaluated on a case-by-case basis in other EU territory.