Document Center List of Standards on Sterilization And Disinfection
ICS Code 11.080
Return to ICS Index.Up to Level 1:
Down to Level 3:
- 11.080.01 (Sterilization and disinfection in general Including sterilization methods, air quality of surgery rooms, etc.)
- 11.080.10 (Sterilizing equipment)
- 11.080.20 (Disinfectants and antiseptics Chemicals for industrial and domestic disinfection purposes, see 71.100.35)
- 11.080.30 (Sterilized packaging)
- 11.080.99 (Other standards related to sterilization and disinfection)
The following documents are a part of this series:
BSI:
IEC:
Other SDOs:
- EN-867-2 - Part 2: Process Indicators (Class a), Non-Biological Systems for Use in Sterilizers
- SS-EN-1040 - Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics - Test method and requirements (phase 1)
- SS-EN-1174-1 - Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 1: Requirements
- SS-EN-1174-2 - Sterilization of medical devices - Estimation of the population of micro-organisms on product - Part 2: Guidance
- SS-EN-1174-3 - Sterilization of medical devices - Estimation of the population of micro-organisms on products - Part 3: Guide to the methods for validation of microbiological techniques
- SS-EN-12353 - Chemical disinfectants and antiseptics - Preservation of test organisms used for the determination of bactericidal (including Legionella), mycobactericidal, sporicidal, fungicidal and virucidal (including bacteriophages) activity
- SS-EN-1275 - Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of basic fungicidal or basic yeasticidal activity of chemical disinfectants and antiseptics - Test method and requirements (phase 1)
- SS-EN-1276 - 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)
- SS-EN-1499 - Chemical disinfectants and antiseptics - Hygienic handwash - Test method and requirements (phase 2/step 2)
- SS-EN-1500 - Chemical disinfectants and antiseptics - Hygienic handrub - Test method and requirements (phase 2/step 2)
- SS-EN-1650 - 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)
- SS-EN-550 - Sterilization of medical devices - Validation androutine control of ethylene oxide sterilization
- SS-EN-552 - Sterilization of medical devices - Validation androutine control of sterilization by irradiation
- SS-EN-552-AM1 - Sterilization of medical devices - Validation and routine control of sterilization by irradiation
- SS-EN-552-AM2 - Sterilization of medical devices - Validation and routine control of sterilization by irradiation
- SS-EN-554 - Sterilization of medical devices - Validation androutine control of sterilization by moist heat
- SS-EN-556 - Sterilization of medical devices - Requirements for terminally-sterilized medical devices to be labelled "Sterile"
- SS-EN-866-1 - Biological systems for testing sterilizers and sterilization processes - Part 1: General requirements
- SS-EN-866-2 - Biological systems for testing sterilizers and sterilization processes - Part 2: Particular systemsfor use in ethylene oxide sterilizers
- SS-EN-866-3 - Biological systems for testing sterilizers and sterilization processes - Part 3: Particular systemsfor use in moist heat sterilizers
- SS-EN-866-5 - Biological systems for testing sterilizers and sterilization processes - Part 5: Particular systems for use in low temperature steam and formaldehyde sterilizers
- SS-EN-866-6 - Biological systems for testing sterilizers and sterilization processes - Part 6: Particular systems for use in dry heat sterilizers
- SS-EN-866-7 - Biological systems for testing sterilizers and sterilization processes - Part 7: Particular requirements for self-contained biological indicator systems for use in moist heat sterilizers
- SS-EN-866-8 - Biological systems for testing sterilizers and sterilization processes - Part 8: Particular requirements for self-contained biological indicator systems for use in ethylene oxide sterilizers
- SS-EN-867-1 - Non-biological systems for use in sterilizers - Part 1: General requirements
- SS-EN-867-2 - Non-biological systems for use in sterilizers - Part 2: Process indicators (Class A)
- SS-EN-867-3 - Non-biological systems for use in sterilizers - Part 3: Specification for Class B indicators for use in the Bowie and Dick test
- SS-EN-867-4 - Non-biological systems for use in sterilizers - Part 4: Specification for indicators as an alternative to the Bowie and Dick test for the detection of steam penetration
- SS-EN-867-5 - Non-biological systems for use in sterilizers - Part 5: Specification for indicator systems and process challenge devices for use in performance testing for small sterilizers Type B and Type S
- SS-EN-868-1 - Packaging materials and systems for medical devices which are to be sterilized - Part 1: General requirements and test methods
- SS-EN-868-10 - Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods
- SS-EN-868-2 - Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
- SS-EN-868-3 - Packaging for terminally sterilized medical devices - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods
- SS-EN-868-4 - Packaging for terminally sterilized medical devices - Part 4: Paper bags - Requirements and test methods
- SS-EN-868-5 - Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods
- SS-EN-868-6 - Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
- SS-EN-868-7 - Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods
- SS-EN-868-8 - Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
- SS-EN-868-9 - Packaging for terminally sterilized medical devices - Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methods
- SS-EN-ISO-11138-1 - Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2017)
- SS-EN-ISO-11138-2 - Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2017)
- SS-EN-ISO-11138-3 - Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2017)
- SS-EN-ISO-11138-4 - Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2017)
- SS-EN-ISO-11138-5 - Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2017)
- SS-EN-ISO-11737-2 - Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)
- SS-EN-ISO-14160 - Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO 14160:2020)
- SS-EN-ISO-14937 - Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)
- SS-EN-ISO-8669-2 - Urine collection bags - Part 2: Requirements and test methods (ISO 8669-2:1996)