Met jarenlange expertise op het gebied van microbiologie, medische technologie en laboratoriumanalyse. Evalueren wij sinds 1993 antimicrobiële en (anti-)klevende eigenschappen van oppervlakken. Dit omvat de methoden als ASTM E 2180, ASTM E 2149, JIS Z 2801 / ISO 22196, JIS L 1902 / ISO 20743, ISO 846, ISO 16869 en AATCC 100.
U kunt ook terecht voor Bio-compatibiliteit testen volgens EN 10933 of het testen van desinfectiemiddelen EN 14885. We breiden ons portfolio continu uit. Neem gerust contact met ons op om u wensen te bespreken.
| Onderzoek | Norm |
| Cytotoxcity Irritation Sensitivity | |
| Analysing which steps to made in the Biological test. Starting price at | ISO 10993-1 |
| Genotoxicity carcinogenicity and reproductive toxicity test | ISO 10993-3 |
| Hemocompatibility test (selection of tests for interaction with Blood) | ISO 10993-4 |
| Cytotoxicity test, Neutralrot Methode, standaard test | ISO 10993-5 |
| Test for local effects after implantation | ISO 10993-6 |
| Ethylene oxide sterilization residuals | ISO 10993-7 |
| Irritation test. In-vitro RhE (nieuwe uitvoerende norm ISO 10993-23) | ISO 10993-10 |
| Sensitivity Direct Peptide Reactivity Assay (DPRS), OECD 442C, Twee media, tweevoud bepaling. In-Vitro | ISO 10993-10 |
| Sensitivity Direct Peptide Reactivity Assay (DPRS), OECD 442C, Twee media, tweevoud bepaling, ieder volgende product. In-Vitro | ISO 10993-10 |
| Sensitivity ARE-Nrf2 Luciferase Testmethod, OECD TG 442D, Twee media, tweevoud bepaling. In-Vitro | ISO 10993-10 |
| Sensitivity ARE-Nrf2 Luciferase Testmethod, OECD TG 442D, Twee media, tweevoud bepaling, ieder volgende product. In-Vitro | ISO 10993-10 |
| Sensitivity Magnusson-Kligman-Test (maximization test) | ISO 10993-10 |
| Sensitivity Closed Patch test (Buehler) | ISO 10993-10 |
| Sensitivity Local Lymph Node Assay test (LLNA) | ISO 10993-10 |
| Test for systemic Toxcity (Bijlage G). LAL test met 2 concetraties 100% en 10%. | ISO 10993-11 |
| Sample preparation and reference materials | ISO 10993-12 |
| Indentification and quantification of degradation products from polymeric medical devices | ISO 10993-13 |
| Indentification and quantification of degradation products from ceramics | ISO 10993-14 |
| Indentification and quantification of degradation products from metals and alloys | ISO 10993-15 |
| Toxicokinetic study design for degradation products and leachables | ISO 10993-16 |
| Establishment of allowable limits for leachable substances | ISO 10993-17 |
| Chemical characterization of medical device materials within a risk management process, prijs vanaf | ISO 10993-18 |
| Principles and methods for immunotoxicology testing of medical devices | ISO 10993-20 |
| Guidance on nanomaterials | ISO 10993-22 |
| Irritation test. In-vitro RhE | ISO 10993-23 |
| Microbiologisch Schimmels | |
| Schimmel onderzoek | DG-18 |
| Schimmel onderzoek | MEA |
| Schimmel onderzoek | MEAP/S |
| Schimmel onderzoek | TSA |
| Schimmel / Mould / Fungi onderzoek, Micorscopisch/kiemgehalte | Method 10-1-002 |
| Bederfelijke goederen onderzoek (max 5 plekken op een aangeleverd goed) | ASU/ LFGB B 80.00.3 |
| Bederfelijke goederen onderzoek (max 5 plekken op een aangeleverd goed) | ASU/ LFGB B 80.00.3 |
| Bepaling van de effecten van microscopisch kleine schimmels (microschimmels) eerste staal | EN 14119 |
| Bepaling van de effecten van microscopisch kleine schimmels (microschimmels) ieder volgend staal | EN 14119 |
| Antifunges onderzoek Schimmels | |
| Environmental Testing Procedures Test J And Guidance: Mould Growth | EN IEC DIN 60068-2-10 |
| Beoordeling van het gedrag van micro-organismen | ISO 846 methode A |
| Beoordeling van het gedrag van micro-organismen | ISO 846 methode B |
| Beoordeling van het gedrag van micro-organismen | ISO 846 methode C |
| Beoordeling van het gedrag van micro-organismen | ISO 846 methode D |
| Optics and optical instruments - Environmental test methods - Part 11: Mould growth | ISO 9022-11 |
| Antifungal Activity, Assessment on Textile Materials: Mildew and Rot Resistance of Textile Materials, Soil Burial | AATCC 30 test I |
| Antifungal Activity, Assessment on Textile Materials: Mildew and Rot Resistance of Textile Materials, Agar plate Chaetomium Globosum | AATCC 30 test II |
| Antifungal Activity, Assessment on Textile Materials: Mildew and Rot Resistance of Textile Materials, Agar plate Aspergillus Niger | AATCC 30 test III |
| Antifungal Activity, Assessment on Textile Materials: Mildew and Rot Resistance of Textile Materials, Humidity Jar, mixed spore suspension | AATCC 30 test IV |
| Determining Resistance of synthetic polymeric Materials to Fungi | ASTM G21 |
| Antifungal Activity, 4 germs, material leather. (Aspergillus sp., Penicillium sp., Trichoderma viride, Hormoconis resinae) | Tegewa method |
| Antifungal Activity, 3 germs, material foam (Aspergillus sp., Penicillium sp., Trichoderma viride ) | Tegewa method |
| Microbiologisch (**) | |
| TPC Total plate count (Totaal van schimmels, gisten en bacterien) | Hygicult |
| E VRBG agar groei van Enterobacteriaccae | Hygicult |
| E VRBG/β-GUR agar groei van Enterobacteriaccae en β-glucuronidase positive microbs | Hygicult |
| CF VRB agar detection of coliforms | Hygicult |
| Y&F Malt agar dor detection of fungi Yeast and mold (Totaal van schimmels en gisten) | Hygicult |
| Bacterie onderzoek, Micorscopisch/kiemgehalte | Method 10-3-001 |
| Antibacterieel onderzoek (**) | |
| Textile fabrics — Determination of antibacterial activity — Agar diffusion plate test | DIN EN ISO 20645 |
| Textiles — Determination of antifungal activity of textile products — Part 2: Plate count method | ISO 13629-2 |
| Medical microbiology - Susceptibility testing of microbial pathogens to antimicrobial agents - Part 3: Agar diffusion test | DIN 58940-3 |
| Antimicrobial Activity of Immobilized Antimicrobial Agents Under Dynamic Contact Conditions 1 kiem 1 ref. 1 materiaal | ASTM E 2149 |
| Antimicrobial Activity of Immobilized Antimicrobial Agents Under Dynamic Contact Conditions 2 kiemen 1 ref. 1 materiaal | ASTM E 2149 |
| Antibacterial Finishes on Textile Materials | AATCC 100 |
| Antimicrobial Activity Assessment of Carpets | AATCC 174 |
| Antibacterial activity to bacteria on antibacterial deodorant finished or microbial control finished textile products | JIS L 1902 |
| Measurement of antibacterial activity on plastics and other non-porous surfaces, 2 kiemen 1 ref. 1 materiaal | ISO 22196 |
| Activity of Incorporated Antimicrobial Agent(s) In Polymeric or Hydrophobic Materials 2 kiemen 1 ref. 1 materiaal | ASTM E 2180 |
| Kill time test | ASTM E 2315 |
| Tests for antimicrobial efficacy | JIS Z 2801 |
| Determination of antibacterial activity of antibacterial finished products | ISO 20743 |
| Determination Of The Resistance Of Textiles To Mildew; Growth Test | DIN 53931 |
| Footwear and footwear components -- Test method to assess antibacterial activity | ISO 16187 |
| Footwear and footwear components — Quantitative challenge test method to assess antifungal activity | EN ISO 20150 |
| Paper and board intended to come into contact with foodstuffs - Determination of the transfer of antimicrobial constituents | EN 1104 |
| Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products | EN 11737-1 |
| Desinfectie Antibacterieel onderzoek (**) | |
| Chemische desinfectantia en antiseptica - Kwantitatieve suspensieproef voor de bepaling van de standaard bacteride werking van chemische desinfectantie en antiseptica | EN 1040 |
| Chemische desinfectantia en antiseptica - Kwantitatieve suspensieproef voor de bepaling van de standaard fungicide of schimmelwerking van chemische desinfectantia en antiseptica | EN 1275 |
| Chemische desinfectantia en antiseptica - Kwantitatieve suspensieproef voor de bepaling van de bactericidewerking van chemische desinfectantia en antiseptica gebruikt in voedsel, in industriële, huishoudelijke en institutionele omgeving | EN 1276 Phase 2 Level1 |
| Chemische desinfectantia en antiseptica - Kwantitatieve suspensietoets voor de bepaling van de fungicide-werking van chemische desinfectantia en antiseptica gebruikt in de voedingsmiddelen-, industriëlele, huishoudelijke en institutionele sector | EN 1650 Phase 2 Level1 |
| Disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants | EN 14348 Phase2 Level1 |
| Kwantitatieve suspensietest voor de evaluatie van bactericide-werking tegen legionella pneumophila van chemische desinfectantia voor waterige vloeistofsystemen | EN 13623 |
| Kwantitatieve suspensietest voor de evaluatie van fungicidal or yeasticidal activity in the medical area | EN 13624 |
| Chemische desinfectantia en antiseptica Quantitative non-porous surface test for the evaluation of bactericidal and/or fungicidal activityof chemical disinfectants used in food, industrial, domestic and institutional areas. | EN 13697 |
| Chemical disinfectants and antiseptics - Hygienic handrub | EN 1500 Phase2 Level2 |
| Chemical disinfectants and antiseptics – Quantitative suspension test for the evaluation of bactericidal activity in the medical area | EN 13727 |
| Minimum requirements for bactericidal and yeasticidal activity of chemical disinfectant products (wipes) Oppervlakte reiniging. | EN 16615 Phase2 Level2 |
| Testing the efficacy of surgical hand antiseptics | EN 12791 |
| Testing the efficacy of surgical hand antiseptics | EN 12791 |
| Testing the efficacy of surgical hand antiseptics | EN 12791 |
| Testing the efficacy of surgical hand antiseptics | EN 12791 |
| Testing the efficacy of surgical hand antiseptics (sreening) | EN 12791 |
| Chemical disinfectants and antiseptics. Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area. | EN 14562 phase 2, step 2 |
| Anti Virus onderzoek (**) | |
| Hygienic handrub and handwash | |
| Limited virucidal activity against enveloped viruses, with Vaccinnia virus, Suspention test. | EN 14476 Phase2 Level1 |
| Limited virucidal activity PLUS, with Adenovirus and Murine-norovirus, Suspention test. | EN 14476 Phase2 Level1 |
| Virucidal activity with Adenovirus, Murine-norovirus and Poliovirus, Suspention test. | EN 14476 Phase2 Level1 |
| Instrument desinfection | |
| Virucidal activity with Adenovirus, Murine-norovirus and Poliovirus. Temperature below 40°C, Suspention test. | EN 14476 Phase2 Level1 |
| Virucidal activity with Adenovirus, Murine-norovirus and Poliovirus. Temperature below 40°C, Carrier test | EN 17111 Phase2 Level2 |
| Virucidal activity with Murine-parvovirus. Temperature above 40°C, Carrier test | EN 17111 Phase2 Level2 |
| Surface desinfection | |
| Limited virucidal activity against enveloped viruses, with Vaccinnia virus, Suspention test. | EN 14476 Phase2 Level1 |
| Limited virucidal activity PLUS, with Adenovirus and Murine-norovirus, Suspention test. | EN 14476 Phase2 Level1 |
| Virucidal activity with Adenovirus, Murine-norovirus and Poliovirus, Suspention test. | EN 14476 Phase2 Level1 |
| Limited virucidal activity against enveloped viruses, with Vaccinnia virus, Carrier test | EN 16777 Phase2 Level2 |
| Limited virucidal activity PLUS, with Adenovirus and Murine-norovirus, Carrier test | EN 16777 Phase2 Level2 |
| Virucidal activity with Adenovirus, Murine-norovirus and Poliovirus, Carrier test | EN 16777 Phase2 Level2 |
| Textile desinfection | |
| Chemothermal disinfection procedure including textile disinfection ≥30°C Murine Parvovorus | EN 14476 Phase2 Level1 |
| Bepaling van de antivirale werking van textiel producten | EN 18184:2019 |
| Measurement of antiviral activity on plastics and other non-porous surfaces Bovine COVID onderzoek (BCoV) | ISO 21702 |
| Biologisch afbreekbaarheid (***) | |
| Biologisch afbreekbaarheid na 3 maanden | EN 13432 |
| Biologisch afbreekbaarheid na 6 maanden | EN 13432 |
| Biologisch afbreekbaarheid na 2 maanden NON GLP | ISO 11734 |
| Biologisch afbreekbaarheid na 2 maanden GLP | ISO 11734 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. certificering) | ASTM D5271 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. certificering) | EN 29408 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. certificering) | ISO 9408 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. certificering) | ISO 14851 |
| Biologisch afbreekbaarheid verlenging van 2 weken (t.b.v. certificering) | ASTM D5271 |
| Biologisch afbreekbaarheid verlenging van 2 weken (t.b.v. certificering) | EN 29408 |
| Biologisch afbreekbaarheid verlenging van 2 weken (t.b.v. certificering) | ISO 9408 |
| Biologisch afbreekbaarheid verlenging van 2 weken (t.b.v. certificering) | ISO 14851 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. screening) | ASTM D5271 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. screening) | EN 29408 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. screening) | ISO 9408 |
| Biologisch afbreekbaarheid na 4 weken (t.b.v. screening) | ISO 14851 |
| Biologisch afbreekbaarheid verlenging van 2 weken (t.b.v. screening) | ASTM D5271 |
| Biologisch afbreekbaarheid verlenging van 2 weken (t.b.v. screening) | ISO 9408 |
| Compostering van verpakkings materialen, Extraction, quantitative (Substances, soluble in Organic Solvents) | DIN 54278-1 |
| Diverse | |
| Resistance to permeation to cytostatica | ISO 6529 |
| Resistance to permeation to cytostatica | ASTM F 739-07 |
| Resistance to permeation to alcohol | ISO 6529 |
| Resistance to permeation to alcohol | ASTM F 739-07 |
| Sterilization of medical devices. Determination of a population of microorganisms on products | Din EN ISO 11737-1 |
| Sterilization of medical devices. Tests of sterility performed in the validation of a sterilization process. | Din EN ISO 11737-2 |
| Sterilization; sterile supply; sterilization paper for bags and tube packings; | Din 58953-6 |
| Microbiological requirements and test methods for products and regimens for hygienic management of contact lenses | Din EN ISO 14729 |
| Antimicrobial preservative efficacy testing and guidance on determining discard date | Din EN ISO 14730 |
| Analyse (aanwezigheid) TVC’ s, E-coli, Listeria & Salmonella |
