Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1 (ISO 11607-2:2006/DAM 1:2013), EN ISO 11607-2:2006/A1
Washer-disinfectors - Part 4: Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endoscopes, ISO 15883-4
Processing of cell-based health care products — Control of microbial contamination, ISO 18362
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems - Amendment 1 (ISO 11607-1:2006/DAM 1:2013), EN ISO 11607-1:2009/A1
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO/FDIS 11137-2:2013), EN ISO 11137-2
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose, ISO 11137-2
Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in human medicine - Test method and requirements (phase 2/step 2), NWIP 216WG1
Revision of ISO 17664:2004, ISO 17664
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in food, industrial, domestic and institutional areas - Test method and requirements (phase 2, step 1), EN 1650:2008/A1
. . ., SIS HB 600-7
Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO/DIS 11140-1:2012), EN ISO 11140-1
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices, EN 556-2
SIS Handbok 600, SIS HB 600
Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of bactericidal and/or fungicidal activity of chemical disinfectants used in food, industrial, domestic and institutional areas - Test method and requirements without mechanical action (phase 2, step 2), EN 13697
Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing, EN 14180
Small steam sterilizers, EN 13060
Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - (phase 2, step 2), EN 16438
Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (phase 2, step2), EN 16437
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006/FDAM 1:2013), EN ISO 11137-1:2006/A1
Washer-disinfectors - Part 1: General requirements, terms and definitions and tests - Amendment 1, EN ISO 15883-1:2009/A1
Chemical disinfectants and antiseptics - Surgical hand disinfection - Test method and requirements (phase 2, step 2)", EN 12791
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1), EN 14675
Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of bactericidal and yeasticidal activity on non-porous surfaces with mechanical action employing wipes in the medical area (4- field test) - Test method and requirements (phase 2, step 2),
Chemical disinfectants and antiseptics - Chemical-thermal linen disinfection - Test method and requirements (phase 2, step 2), EN
Sterilization of health care products - Chemical indicators - Part 1: General requirements, ISO 11140-1
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), EN 14476
Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods, EN 1422
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2011/FDAM 1:2013), EN ISO 13408-1:2011/A1
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2012), EN ISO 11135
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices, ISO 11137-1:2006/Amd 1
Washer-disinfectors - Part 1: General requirements, terms and definitions and tests - Amendment 1, ISO 15883-1/Amd 1
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1, ISO 11607-2:2006/Amd 1
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems, ISO 11607-1:2006/Amd 1
Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2), EN 1500
Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2), EN 1499
Test method to demonstrate the suitability of a medical device simulator during steam sterilization - Medical device simulator testing, ISO 17210
Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices, ISO 11135
Washer-disinfectors - Part 7: Requirements and tests for general purpose washer-disinfectors employing chemical disinfection for bedframes, bedside tables, transport carts, containers, surgical tables, furnishings and surgical clogs, ISO 15883-7
Sterilization tape, N941 NWIP steril tejp
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1), EN 13624
Sterilization of medical devices - low temperatur steam and formaldehyde - Requirements for development , validation and routine control of a sterilization process for medical devices, EN ISO 15424
Sterilization of medical devices - Microbiological methods - Part 4: Sterility test on sterile medical devices, ISO 11737-4
Sterilization of health care products - Biological indicators - Method for validation of a reduced incubation time for a biological indicator, ISO/TS 16342
Sterilization of health care products - Biological Indicators - Part 6: Biological indicators for hydrogen peroxide vapour sterilization processes, EN ISO 11138-6
Sterilization of health care products - Biological Indicators - Part 6: Biological indicators for hydrogen peroxide vapour sterilization processes, ISO 11138-6
Guidance on the application of ISO 11607-1 and ISO 11607-2 Packaging for terminally sterilized medical devices, EN ISO 16775
Sterilization of health care products - Radiation - Substantiation of selected sterilization doses: Method VDmaxSD, ISO/TS 13004
Controlled environment storage cabinet for disinfected thermolabile endoscopes, EN 16442