Design Idea

Staron® evermoin®

More Innovation, More Integration
Solution for

The healthiest choice for your design

evermoin® anti-microbial surfaces from staron® can be applied to almost any interior space within a healthcare facility.
Imagine casework, work-stations and wall-cladding in a functional and renewable material that is durable as well as ultra-hygienic. Achieve the perfect blend of simplicity in design in an anti-microbial surface engineered for a healthier life.

Benefit of evermoin®

  • Antimicrobial

    Speedy antibacterial effect and action on representative bacteria and fungi

  • Durability

    Excellent antimicrobial retention and Confirm quality stability and durability

  • Safety

    Material certification harmless to human body and environment
    (SIAA, NSF, FDA)

Ultra Bright



W.3680 x L.760 x 12T [mm]
W.2500 x L.760 x 6T [mm]

Doctor’s office, Operation room
Nurse station
Disinfection room

evermoin® has been approved by following certification bodies

  • SIAA

    Society of International sustaining growth for Antimicrobial Articles

  • NSF

    National Sanitation Foundation

  • FDA

    US Food & Drug Administration

evermoin® has passed following tests

  • - ASTM E 2180 (Standard test method for determining the activity of incorporated antimicrobial agent)
  • - ISO 846 B' (Test method for determining of fungistatic effect)
  • - FDA 21 CFR 177 (Food contact testing)

ASTM E 2180 (Bacteria Test)

- Exposed a testing plece to bacteria for 24 hours (provided nutrient) ▶ killed 99.9% of bacteria

Blank Evermoin Note
Staphylococcus aureus
ATCC 6538
“0” h control 3.0 x 106 3.0 x 106 Sample surface area :
(3 x 3) cm
Inoculum volume :
0.5 mL
Neutralizing broth :
After 24 h 2.8 x 108 2.5 x 104
Percent reduction of Bacteria - 99.1%
Klebsiella pneumoniae
ATCC 4352
“0” h control 2.0 x 106 2.0 x 106
After 24 h 3.5 x 107 8.7 x 102
Percent reduction of Bacteria - 99.9%

ISO 846 [B’] (Antifungal test)

- Obtained with SGS EN ISO 846 B’ fungistatic effect grade 0

Test Method Test Condition Test Result Test Organization
ISO 846 B’ Incubation at 30℃ for 4 weeks Strong fungistatic effect (0) SGS
Intesity of growth Organization
0 No growth apparent under the microscope
1 No growth visible to the naked eye, but clearly visible under the microscope
2 Growth visible to the naked eye, covering up to 25% of the test surface
3 Growth visible to the naked eye, covering up to 50% of the test surface
4 Considerable growth, covering more than 50% of the surface
5 Heavy growth, covering the entire test surface

FDA 21 CFR 177 (Human safety Test)

- Complying with 21 CFR 177.1010 of U.S FAD (Food and Drug Administration)

Intesity of growth Conclusion
a) Total Nonvolatile Extractives PASS
b) Potassium Permanganate Oxidizable Extractives PASS
c) Ultraviolet-absorbing Extractives PASS
Extractants Test Condition Result (mg / inch2) Reporting Limit
(mg / inch2)
Permissible Limit
(mg / inch2)
Distilled Water 120℉ for 24 hours 0.16 PASS PASS
8% Alcohol 120℉ for 24 hours 0.15 PASS PASS
N-Heptane 70℉ for 30 minutes 0.06 PASS PASS
Comment - PASS - -