Our technology is evidence based and we always rely on 3rd party validation of the product(s). Microbiological Solutions Ltd., London; Centexbel, Belgium; VITO, Belgium; Japan Food Research Laboratories; Kyoto Microbiological Laboratory, Japan; Kaken test Center, Japan; SITRA, India; Intertek, India; Turkak, Turkey; VRDL, India; The Aachen-Maastricht Institute for Biobased Material; ...

Patent pending at United States Patent and Trademark Office (USPTO)

Efficacy:

Our Silver products have shown powerful and fast bactericidal activity assessed by American (ASTM E 2149) and Japanese (JIS L 1902) reference methods in several accredited testing laboratories.

It eliminated Staphylococcus aureus (including MRSA), Escherichia coli, Klebsiella pneumoniae, Pseudomonas aeruginosa and Salmonella enteritidis to below the detection limit in less than 1 hour. In some test, complete bacterial killing was observed in less than 1 minute.

The viricidal activity was demonstrated in various protocols by us, clients and research partners. We saw that 1 layer of our Silver fabric on average eliminates +90% of any virus within minutes upon contact. We use 2 layers of silver fabric in our masks. This combination can eliminate more than 99% of the virus INSTANTLY on contact with our SUPRMASK. The filters we use show an efficiency of 99,48%. (SUPRMASK Pro and Premium). The total mask reduces immediately the impact of the virus by 99,99%. 

Test were performed according to protocol ISO 18184:2019 (Determination of antiviral activity of textile products). ISO 18184 is an antiviral textile test that measures virucidal antimicrobial activity on textiles and other porous materials. The ISO 18184 test standard is designed to test the ability of textiles and other similar materials to kill virus. Standard virus exposure times range from 2 hours to less than 24 hours.

Reduction in Virus Viability (%) 
(minutes) 0 5 10 30 60 120 240
Feline Calici Coronavirus* 88,27 90,90 92,60 94,28 99,14 99,82
Influenzavirus H3N2* 90,60 95,55 98,32 99,94 99,98 99,9991
Influenzavirus H1N1* 77,18 94,38 96,66 99,42 99,89 99,92 99,993
Coronavirus 229E* ***
87,41 92,92 98,42 98 99,84 99,87 99,9994
Influenzavirus H1N1 (lab)**
80,50 97,18 99,62
Coronavirus 229E (lab)** 78,62 98,34 99,81
* tests performed according to a slightly modified ISO 18184:2019 protocol to match the real world
** tests strictly performed according to ISO 18184:2019 protocol, which is not a representation of the real world!
*** ASTM (American Society for Testing and Materialsadvises 229E as the best alternative to SARS-CoV-2 (see ASTM: Guidance on SARS-CoV-2 Surrogate Selection

 

 

The virucidal activity of silver was shown in various independent research protocol.

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The fungicidal activity of our Silver products against Trychophyton mentagrophytes was demonstrated in the JIS L 1902 test. After less than 3 hours of incubation, no colony forming units were detectable.

Regulatory Compliance:

Classification according to Medical Devices Directive 93/42/EEC and Medical Devices Regulation (EU) 2017/745

Medical Face Masks are classified according to Rule 1 for non-invasive devices, as devices that either do not touch the patient or contact intact skin only.

Click here for the Declaration of Conformity for one of our masks.

Classification according to the harmonised European and British standard BS EN 14683:2019+AC:2019

Medical face masks are classified as Type I and Type II according to bacterial filtration efficiency, whereby Type II is further divided (Type II and IIR) according to whether or not the mask is splash resistant. The 'R' signifies splash resistance.

Type I medical face masks should only be used for patients and other persons to reduce the risk of spread of infections particularly in epidemic or pandemic situations. Type I masks are not intended for use by healthcare professional in an operating room or in other medical settings with similar requirements.

Our masks have been tested at the following centers with its corresponding results:

1. SUPRMASK Pro according to BS EN 14683:2019+AC:2019 at Centexbel, Belgium [Medical Device Surgical Mask Type IIR/3]. Similar results were obtained at The Aachen-Maastricht Institute for Biobased Material.

2. SUPRMASK Premium at South India Textile Research Association, India

  • Bacterial Frequency Efficiency (ASTM F2101) of 99,8% [≥ 98%] with mean particle size of 3.0 μm [≥ 3,0]
  • Breathability (Differential Pressure) (ISO 16289-2014) of 28,0 Pa/cm2 [≤ 60]
  • Particle Filtration Efficiency (ASTM F2299/F2299M-03 - 2010) of 98.89 % [≥ 95%] with mean particle size of 0.3 μm [≥ 0,3]

3. SUPRMASK Basic according to BS EN 14683:2019+AC:2019 at Centexbel, Belgium [Medical Device Surgical Mask Type I]

  • Bacterial Frequency Efficiency of 95,75 % [≥ 95%] with mean particle size of 2.8 μm [≥ 3,0]
  • Breathability (Differential Pressure) of 13,8 Pa/cm2 [≤ 40]

4. SUPRMASK Medical at South India Textile Research Association, India

  • Bacterial Frequency Efficiency (ASTM F2101) of 99,5 % [≥ 98%] with mean particle size of 3.0 μm [≥ 3,0]
  • Breathability (Differential Pressure) (ISO 16289-2014) of 20,0 Pa/cm2 [≤ 60]
  • Particle Filtration Efficiency (ASTM F2299/F2299M-03 - 2010) of 98.82 % [≥ 95%] with mean particle size of 0.3 μm [≥ 0,3]

Safety:

Safety and biocompatibility was proven in a few in vitro studies. (Japan Food research Laboratories)

  • No skin sensitization was observed in compliance with ISO 10993-10:2010 (Biological evaluation of medical devices – Part 10: Test for irritation and skin sensitization)
  • No skin irritation was observed in compliance with ISO 10993-10:2010 (Biological evaluation of medical devices – Part 10: Test for irritation and skin sensitization)
  • No cytotoxicity was observed in compliance with ISO 10993:2009 (Biological evaluation of medical devices – Part 5: Test for in vitro cytotoxicity)
  • No risk was observed on the inhalation of silver particles. The level of particles that were inhaled remained far below safety norms.
  • No heavy metals are used in the manufacturing process. (Directive 2002/95/EC of the European Parliament and of the Council of 27 January 2003)
  • No sulphur based chemicals, sulphates, bromine, chlorine gas, organics etc are used in the production process.
  • The water after our production process is processed by our own Effluent Treatment Plant and used to water the gardens. Hence, there is no net release of water into streams etc.
  • We have permits which allows us to do the effluent treatment process. The water after treatment is tested by independent laboratories every month and also by the Government authorities on a random basis. We are always in compliance with local laws and regulations
  • Once our silver comes in wastewater it will not negatively impact the effluent water treatment. Our tests have shown reduction of Biochemical Oxygen Demand (BOD) in wastewater.
  • Silver is obtained from vendors who possess valid licenses issued by the Government. This way we know silver procured is from legitimate sources
  • Silver, being precious and a very important metal, can be safely recycled back to its native state. This way there is no net loss of resources of such a fantastic metal
  • All silvers are not equal. Silver in nano size can potentially cause significant damage to aquatic lives and also on earth. Our silver has certain unique properties whereby they are always safe and work optimally. We have 3rd party testing showing our product is safe on skin, etc.

Various research articles have shown the safety profile of silver.

See more literature

      Interested in a Research Collaboration, please email us

       

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