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Insights · Testing & evidence

Test standards for antimicrobial materials: which standard measures what?

6 min readUpdated October 2026

In short

Key standards for antimicrobial materials are ISO 22196 or JIS Z 2801 (plastics, non-porous surfaces), ISO 20743 (textiles) and ASTM E2149 (dynamic contact). EN 1276, EN 13697, EN 14476 and EN 1500 test disinfectants; ISO 10993-5 tests the cytotoxicity of medical devices. Results are usually log reductions: 2 log means 99 %, 4 log 99.99 % fewer viable microorganisms.

Petri dishes holding square white plastic test specimens, each with a thin cover film over a small drop
Illustrative image
Test set-up to ISO 22196: specimen 50 × 50 mm, cover film 40 × 40 mm

Standards Navigator: find the right standard.

Choose a material and a claim. The navigator shows the matching standards with what they measure, the conditions and how to read the result.

Choose a material and a claim. The navigator shows the matching standards with what they measure, the conditions and how to read the result.

  1. 01

    Define the material

    plastic, textile, other non-porous surface, liquid product or medical device.

  2. 02

    Define the claim

    antibacterial, antiviral, protection of the material, disinfection or biocompatibility.

  3. 03

    Compare the conditions of use with those of the standard and add a second method closer to the application if needed.

Material

Claim

  • ISO 22196:2011

    Measurement of antibacterial activity on plastics and other non-porous surfaces

    Material
    Plastics and other non-porous surfaces; standard specimen 50 × 50 mm, no more than 10 mm thick
    Organisms
    Staphylococcus aureus (e.g. ATCC 6538P) · Escherichia coli (e.g. ATCC 8739)
    Conditions
    0.4 ml bacterial suspension (2.5–10 × 10⁵ cells/ml) under a 40 × 40 mm cover film; 24 h at 35 °C and at least 90 % relative humidity
    How to read the result
    Antibacterial activity R = log difference in viable bacteria between untreated and treated specimens after 24 h. R = 2 means 99 % fewer viable bacteria. The standard sets no pass level; the parties involved agree on it.

    Plastics & masterbatchPaints & coatingsPackagingTouch surfacesMedical devices

  • JIS Z 2801:2010

    Antibacterial products – Test for antibacterial activity and efficacy

    Material
    as ISO 22196: plastics and other non-porous surfaces, specimen 50 × 50 mm
    Organisms
    Staphylococcus aureus (e.g. ATCC 6538P) · Escherichia coli
    Conditions
    as ISO 22196: 0.4 ml bacterial suspension under a 40 × 40 mm cover film; 24 h at 35 °C and at least 90 % relative humidity
    How to read the result
    Antibacterial activity R as in ISO 22196. Under JIS Z 2801 (section 4), a product with R of 2.0 or more counts as antibacterially effective. ISO 22196 is based on this standard.

    Plastics & masterbatchPaints & coatingsPackagingTouch surfacesMedical devices

  • ISO 20743:2021

    Textiles – Determination of antibacterial activity of textile products

    Material
    All textile products including nonwovens: fabrics, yarns, materials for clothing, bedding and home furnishings
    Organisms
    Staphylococcus aureus · Klebsiella pneumoniae
    Conditions
    Absorption, transfer or printing method; incubation for 18–24 h at about 37 °C; count by plate counting or ATP luminescence
    How to read the result
    Antibacterial activity value A (log) compared with the untreated control. 2 ≤ A < 3 counts as significant, A ≥ 3 as strong activity.

    TextilesHygiene productsMedical devices

  • ISO 846:2019

    Plastics – Evaluation of the action of microorganisms

    Material
    Plastics
    Organisms
    Moulds, e.g. Aspergillus brasiliensis, Chaetomium globosum, Penicillium pinophilum, Trichoderma virens, Aureobasidium pullulans · Bacteria (method C) · Soil microorganisms (method D)
    Conditions
    Method A: fungal spores without nutrient medium · B: fungal spores with nutrient medium (fungistatic effect) · C: bacteria in a medium without carbon source · D: soil burial; fungal tests at 29 °C and at least 95 % relative humidity, incubation over several weeks
    How to read the result
    Visual growth plus change in mass and physical properties (e.g. flexural properties, impact strength, hardness) against control specimens. Method A shows whether the plastic supports fungal growth; method B whether a biocide it contains inhibits it.

    Plastics & masterbatchTouch surfaces

  • ASTM E2149-25

    Standard Test Method for Determining the Antimicrobial Activity of Antimicrobial Agents Under Dynamic Contact Conditions

    Material
    Antimicrobial-treated specimens, especially fibres, textiles, powders and irregularly shaped surfaces
    Organisms
    Escherichia coli (typically ATCC 25922)
    Conditions
    Specimen in buffer with a defined bacterial suspension; 1 h contact with constant shaking in a flask
    How to read the result
    Reduction in viable bacteria compared with a control tested at the same time, in percent or log. According to the standard, it cannot determine whether a substance leaches or stays bound.

    TextilesHygiene productsWater & membranesPlastics & masterbatch

  • EN 1276:2019

    Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas – Test method and requirements (phase 2, step 1)

    Material
    Chemical disinfectants and antiseptics for food, industrial, domestic and institutional areas
    Organisms
    Pseudomonas aeruginosa ATCC 15442 · Escherichia coli ATCC 10536 · Staphylococcus aureus ATCC 6538 · Enterococcus hirae ATCC 10541
    Conditions
    Product in bacterial suspension; obligatory conditions 20 °C and 5 min; clean (0.3 g/l bovine albumin) or dirty conditions (3.0 g/l)
    How to read the result
    Pass at a reduction of at least 5 log (99.999 %) for each obligatory organism.

    Hygiene productsAnimal hygiene

  • EN 13697:2023

    Chemical disinfectants and antiseptics – Quantitative non-porous surface test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants used in food, industrial, domestic and institutional areas without mechanical action – Test method and requirements (phase 2, step 2)

    Material
    Chemical disinfectants for non-porous surfaces without mechanical action; stainless steel carriers
    Organisms
    Pseudomonas aeruginosa · Escherichia coli · Staphylococcus aureus · Enterococcus hirae · Candida albicans · Aspergillus brasiliensis (fungicidal)
    Conditions
    Organisms dried onto the carrier, then product applied; contact time 1–60 min and temperature 4–40 °C per application; clean or dirty conditions
    How to read the result
    Pass at a reduction of at least 4 log (bactericidal) or 3 log (yeasticidal, fungicidal).

    Hygiene productsAnimal hygiene

  • EN 14476:2025

    Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of virucidal activity in the medical area – Test method and requirements (phase 2, step 1)

    Material
    Chemical disinfectants and antiseptics in the medical area: hand, surface and instrument disinfection
    Organisms
    Poliovirus · Adenovirus · Murine norovirus · Vaccinia virus (enveloped viruses)
    Conditions
    Product in virus suspension; contact time, temperature and interfering substance per application and claim; replaces EN 14476:2013+A2:2019
    How to read the result
    Pass at a titre reduction of at least 4 log. The claim follows from the test viruses: virucidal (polio-, adeno-, murine norovirus), limited spectrum virucidal (adeno-, murine norovirus), active against enveloped viruses (vaccinia virus).

    Hygiene products

  • EN 1500:2013

    Chemical disinfectants and antiseptics – Hygienic handrub – Test method and requirements (phase 2, step 2)

    Material
    Hand disinfectants applied by rubbing
    Organisms
    Escherichia coli K12
    Conditions
    Hands of 18–22 volunteers contaminated; reference 2-propanol 60 %, 2 × 3 ml, 60 s in total; test product as specified by the manufacturer
    How to read the result
    Pass if the product's log reduction is not significantly inferior to that of the reference (non-inferiority test).

    Hygiene products

  • ISO 10993-5:2009

    Biological evaluation of medical devices – Part 5: Tests for in vitro cytotoxicity

    Material
    Medical devices, their materials and extracts
    Organisms
    Mammalian cells, e.g. L929 mouse fibroblasts
    Conditions
    Extract, direct or indirect contact with cultured cells; quantitative read-out e.g. MTT, XTT or neutral red uptake
    How to read the result
    A reduction in cell viability of more than 30 % against the control counts as a cytotoxic effect. The test is part of the biological evaluation under the ISO 10993 series.

    Medical devices

Ten standards at a glance.

Organisms are those named in the standard or typically used. The current edition of each standard applies; the table reflects the status as of 26 September 2026.

StandardWhat is measuredMaterialOrganisms (typical)Contact time, conditionsHow to read the result
ISO 22196:2011 [1]antibacterial activity of a surfaceplastics, non-porous surfaces; specimen 50 × 50 mmStaphylococcus aureus, Escherichia coli0.4 ml bacterial suspension under a 40 × 40 mm cover film; 24 h, 35 °C, ≥ 90 % RHR = log difference to the untreated sample; the pass level is agreed by the parties
JIS Z 2801:2010 [2]as ISO 22196, the Japanese originalas ISO 22196S. aureus, E. colias ISO 22196under JIS, R ≥ 2.0 counts as antibacterial efficacy
ISO 20743:2021 [3]antibacterial activity of textilesfabrics, yarns, nonwovensS. aureus, Klebsiella pneumoniaeabsorption, transfer or printing method; 18–24 h at about 37 °Cactivity value A (log): 2 to below 3 significant, 3 or more strong
ISO 846:2019 [4]resistance to microorganismsplasticsmoulds (e.g. Aspergillus brasiliensis), bacteria, soil organismsmethods A to D; fungal tests at 29 °C, ≥ 95 % RH, several weeksvisual growth, change in mass and properties against control
ASTM E2149-25 [5]activity under dynamic contactfibres, textiles, powders, irregular shapesE. coli (ATCC 25922)sample in buffer with bacteria; 1 h shakingreduction in % or log against control; does not distinguish leaching from non-leaching
EN 1276:2019 [6]bactericidal activity of disinfectants, suspension testdisinfectants and antiseptics for food, industrial, domestic and institutional areasPseudomonas aeruginosa, E. coli, S. aureus, Enterococcus hiraeobligatory conditions 20 °C, 5 min; clean or dirty conditions (albumin)pass at ≥ 5 log reduction
EN 13697:2023 [7]bactericidal, yeasticidal, fungicidal activity on surfaces without mechanical actiondisinfectants; stainless steel disc carriersP. aeruginosa, E. coli, S. aureus, E. hirae; Candida albicans, A. brasiliensisorganisms dried onto the carrier; contact time and temperature per applicationpass at ≥ 4 log (bacteria) or ≥ 3 log (yeasts, moulds)
EN 14476:2025 [8]virucidal activity in the medical area, suspension testhand, surface and instrument disinfectionpolio-, adeno- and murine norovirus; vaccinia virus for enveloped virusestime and temperature per application; replaces EN 14476:2013+A2:2019pass at ≥ 4 log titre reduction
EN 1500:2013 [9]hygienic handrub, test with volunteershand disinfectantsE. coli K1218 to 22 volunteers; reference 2-propanol 60 %, 2 × 3 ml, 60 s in totalpass if not significantly inferior to the reference
ISO 10993-5:2009 [10]in vitro cytotoxicitymedical devices and their extractsmammalian cells, e.g. L929 fibroblastsextract, direct or indirect contact; read-out e.g. MTT, XTT, neutral redviability loss above 30 % against control counts as a cytotoxic effect

Literature

Log Calculator: percent and log reduction.

Microbial counts span many orders of magnitude, so results are given as a base-10 logarithm. Log reduction = log₁₀ (count on control ÷ count on sample). As a percentage: (1 − 10^−log) × 100.

Percent · log reduction · survivors out of 1,000,000

At 99.99 %, 100 out of one million microorganisms remain.

A log value only holds together with the organism, starting count, contact time and conditions. Values from different standards cannot be compared directly.

Worked example, not a test result for Z-Chitosan

4 log equals 99.99 %. Of 1,000,000 microorganisms, 100 remain.

Log reduction = log₁₀ (initial count ÷ remaining count) · Per cent = (1 − 10^−log) × 100

What standards do not show.

Laboratory tests reflect the application only in part. ISO 22196 keeps the inoculum moist and warm for 24 hours; none of these conditions matches a typical end-use environment [12]. In one study, more nutrients in the inoculum lowered the measured effect from over 3 log to under 1 log [13].

The newer ISO 7581:2023 tests non-porous surfaces under dry conditions: 1 µl inoculum, 20 °C, 30–65 % relative humidity, 1 to 2 hours [14, 15]. For ISO 10993-5, too, an interlaboratory study with 52 laboratories found markedly different assessments of the same material [16].

EN 1276, EN 13697, EN 14476 and EN 1500 apply to chemical disinfectants and antiseptics. For materials with a lasting antimicrobial treatment, ISO 22196, ISO 20743 or ASTM E2149 are the suitable methods.

Other claims have standards of their own: ISO 21702 measures antiviral activity on plastics and other non-porous surfaces, ISO 18184 that of textiles. ISO 4768 tests anti-biofilm activity on non-porous surfaces [17, 18, 19].

Literature

For your product

What this means for your product.

The Material Library on the Applications page shows which standard suits your material. For Z-Chitosan, ZCP sets the test plan for each material.

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FAQ

Frequently asked.

Your question isn’t here? Ask the assistant or the team.

What is the difference between ISO 22196 and JIS Z 2801?

ISO 22196 is based on the Japanese JIS Z 2801 [11]. The procedure is the same: bacterial suspension under a film, 24 hours at 35 °C and at least 90 % relative humidity. JIS Z 2801 treats a value of R = 2.0 or more as antibacterial efficacy, while ISO 22196 leaves the pass level to the parties involved.

What does an R value of 2 mean?

R = 2 means that after 24 hours the treated sample carries 2 log fewer viable bacteria than the untreated one, which is 99 % fewer. The value applies to the test conditions of the standard. It cannot be transferred directly to dry surfaces in everyday use.

Which standards does an antimicrobial-coated medical device need?

Usually two groups: a test of antimicrobial performance, for example to ISO 22196 or in a biofilm model, and the biological evaluation under the ISO 10993 series, including cytotoxicity to ISO 10993-5. Class and requirements follow from Regulation (EU) 2017/745.

Author
ZCP editorial team
Status
October 2026 · Editions of standards checked on 26 September 2026
Reading time
6 min
Sources22
  1. ISO 22196:2011: Measurement of antibacterial activity on plastics and other non-porous surfaces. International Organization for Standardization, Genf (zuletzt bestätigt 2026).
  2. JIS Z 2801:2010 (mit Änderung 1:2012): Antibacterial products – Test for antibacterial activity and efficacy. Japanese Standards Association, Tokio.
  3. ISO 20743:2021: Textiles – Determination of antibacterial activity of textile products. International Organization for Standardization, Genf.
  4. ISO 846:2019: Plastics – Evaluation of the action of microorganisms. International Organization for Standardization, Genf.
  5. ASTM E2149-25: Standard Test Method for Determining the Antimicrobial Activity of Antimicrobial Agents Under Dynamic Contact Conditions. ASTM International, West Conshohocken.
  6. EN 1276:2019: Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas – Test method and requirements (phase 2, step 1). Europäisches Komitee für Normung (CEN), Brüssel.
  7. EN 13697:2023: Chemical disinfectants and antiseptics – Quantitative non-porous surface test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants used in food, industrial, domestic and institutional areas without mechanical action – Test method and requirements (phase 2, step 2). CEN, Brüssel (ersetzt EN 13697:2015+A1:2019).
  8. EN 14476:2025: Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of virucidal activity in the medical area – Test method and requirements (phase 2, step 1). CEN, Brüssel (ersetzt EN 14476:2013+A2:2019).
  9. EN 1500:2013: Chemical disinfectants and antiseptics – Hygienic handrub – Test method and requirements (phase 2, step 2). CEN, Brüssel.
  10. ISO 10993-5:2009: Biological evaluation of medical devices – Part 5: Tests for in vitro cytotoxicity. International Organization for Standardization, Genf (zuletzt bestätigt 2022).
  11. Bento de Carvalho T., Barbosa J. B., Teixeira P. (2024): Assessing antimicrobial efficacy on plastics and other non-porous surfaces: a closer look at studies using the ISO 22196:2011 standard. Biology 13(1):59. DOI 10.3390/biology13010059
  12. Cunliffe A. J., Askew P. D., Stephan I., Iredale G., Cosemans P., Simmons L. M., Verran J., Redfern J. (2021): How do we determine the efficacy of an antibacterial surface? A review of standardised antibacterial material testing methods. Antibiotics 10(9):1069. DOI 10.3390/antibiotics10091069
  13. Wiegand C. et al. (2018): Critical physiological factors influencing the outcome of antimicrobial testing according to ISO 22196 / JIS Z 2801. PLOS ONE 13(3):e0194339. DOI 10.1371/journal.pone.0194339
  14. ISO 7581:2023: Evaluation of bactericidal activity of a non-porous antimicrobial surface used in a dry environment. International Organization for Standardization, Genf.
  15. Maitz S., Poelzl S., Dreisiebner D., Zarschenas E., Kittinger C. (2024): Antimicrobial non-porous surfaces: a comparison of the standards ISO 22196:2011 and the recently published ISO 7581:2023. Frontiers in Microbiology 15:1400265. DOI 10.3389/fmicb.2024.1400265
  16. Gruber S., Nickel A. (2023): Toxic or not toxic? The specifications of the standard ISO 10993-5 are not explicit enough to yield comparable results in the cytotoxicity assessment of an identical medical device. Frontiers in Medical Technology 5:1195529. DOI 10.3389/fmedt.2023.1195529
  17. ISO 21702:2019: Measurement of antiviral activity on plastics and other non-porous surfaces. International Organization for Standardization, Genf.
  18. ISO 18184:2019: Textiles – Determination of antiviral activity of textile products. International Organization for Standardization, Genf.
  19. ISO 4768:2023: Measurement method of anti-biofilm activity on plastic and other non-porous surfaces. International Organization for Standardization, Genf.
  20. Inhaltstabellen stehen je Sprache als eigene Markdown-Tabelle („Tabelle B.xx-n (DE)“ / „(EN)“); EN-Zahlen mit Dezimalpunkt.
  21. In B.29 werden die nach Art. 72 Abs. 3 BPR verbotenen Begriffe und die Aussagen aus den Urteilen bewusst zitiert (Erklärung der Rechtslage, keine Produktaussage). Sie stehen immer in Anführungszeichen und dürfen nicht als Aussage über ZCP oder Z-Chitosan wiederverwendet werden.
  22. Grafiken (Etikett-Anatomie, Größenleiter, pH-Diagramm) werden als SVG im Code gebaut; alle Beschriftungen sind echter Text (barrierefrei, übersetzbar).

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