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标准编号 | 标准名称 | 发布日期 | 实施日期 | 废止日期 | 替换信息 |
---|---|---|---|---|---|
ISO/NP 10873 | Dentistry -- Denture adhesives | ||||
ISO 8373:1994/Cor 1:1996 | |||||
ISO 7112:1999 | Machinery for forestry -- Portable hand-held brush-cutters and grass-trimmers -- Vocabulary | ||||
ISO 6935-1:1991 | Steel for the reinforcement of concrete -- Part 1: Plain bars | ||||
ISO 11135-1:2007 | Sterilization of health care products -- Ethylene oxide -- Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices | ||||
ISO/TS 11135-2:2008 | Sterilization of health care products -- Ethylene oxide -- Part 2: Guidance on the application of ISO 11135-1 | ||||
ISO 11137:1995/Amd 1:2001 | Selection of items for dose setting | ||||
ISO 11137:1995 | Sterilization of health care products -- Requirements for validation and routine control -- Radiation sterilization | ||||
ISO 11137-1:2006 | Sterilization of health care products -- Radiation -- Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices | ||||
ISO 11137:1995/Cor 1:1997 | |||||
ISO 11137-2:2006 | Sterilization of health care products -- Radiation -- Part 2: Establishing the sterilization dose | ||||
ISO/IEC 7501-1:1993 | Identification cards -- Machine readable travel documents -- Part 1: Machine readable passport | ||||
ISO 11137-3 | Sterilization of health care products -- Radiation -- Part 3: Guidance on dosimetric aspects of development, validation and routine control | ||||
ISO 11138-1:1994 | Sterilization of health care products -- Biological indicators -- Part 1: General | ||||
ISO 11138-1:2006 | Sterilization of health care products -- Biological indicators -- Part 1: General requirements | ||||
ISO 11138-2:1994 | Sterilization of health care products -- Biological indicators -- Part 2: Biological indicators for ethylene oxide sterilization | ||||
ISO 11138-2:2017 | Sterilization of health care products -- Biological indicators -- Part 2: Biological indicators for ethylene oxide sterilization processes | ||||
ISO 11138-3:1995 | Sterilization of health care products -- Biological indicators -- Part 3: Biological indicators for moist heat sterilization | ||||
ISO 11138-5:2017 | Sterilization of health care products -- Biological indicators -- Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes | ||||
ISO 11138-4:2017 | Sterilization of health care products -- Biological indicators -- Part 4: Biological indicators for dry heat sterilization processes | ||||
ISO 11138-4:2006 | Sterilization of health care products -- Biological indicators -- Part 4: Biological indicators for dry heat sterilization processes | ||||
ISO 11138-5:2006 | Sterilization of health care products -- Biological indicators -- Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes | ||||
ISO 11140-1:1995 | Sterilization of health care products -- Chemical indicators -- Part 1: General requirements | ||||
ISO 11140-1:2014 | Sterilization of health care products -- Chemical indicators -- Part 1: General requirements | ||||
ISO 11140-2:1998 | Sterilization of health care products -- Chemical indicators -- Part 2: Test equipment and methods | ||||
ISO 11140-4:2007 | Sterilization of health care products -- Chemical indicators -- Part 4: Class 2 indicators as an alternative to the Bowie and Dick-type test for detection of steam penetration | ||||
ISO 11737-1:1995 | Sterilization of medical devices -- Microbiological methods -- Part 1: Estimation of population of microorganisms on products | ||||
ISO/CD 11140-6 | Sterilization of health care products -- Chemical indicators -- Part 6: Class 2 indicators and process challenge devices for use in performance testing of steam sterilizers | ||||
ISO 11737-1:2006 | Sterilization of medical devices -- Microbiological methods -- Part 1: Determination of a population of microorganisms on products | ||||
ISO 11140-5:2007 | Sterilization of health care products -- Chemical indicators -- Part 5: Class 2 indicators for Bowie and Dick-type air removal tests | ||||
ISO/TS 13004:2013 | Sterilization of health care products -- Radiation -- Substantiation of selected sterilization dose: Method VDmaxSD | ||||
ISO 11737-3:2004 | Sterilization of medical devices -- Microbiological methods -- Part 3: Guidance on evaluation and interpretation of bioburden data | ||||
ISO 11737-2:1998 | Sterilization of medical devices -- Microbiological methods -- Part 2: Tests of sterility performed in the validation of a sterilization process | ||||
ISO/NP 11737-2 | Sterilization of medical devices -- Microbiological methods -- Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process | ||||
ISO/DIS 11737-1 | Sterilization of health care products -- Microbiological methods -- Part 1: Determination of a population of microorganisms on product | ||||
ISO 11737-2:2009 | Sterilization of medical devices -- Microbiological methods -- Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process | ||||
ISO/DIS 13408-2 | Aseptic processing of health care products -- Part 2: Sterilizing filtration | ||||
ISO 14161:2000 | Sterilization of health care products -- Biological indicators -- Guidance for the selection, use and interpretation of results | ||||
ISO 14160:2011 | 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 14937:2000 | 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/TR 13409:1996 | Sterilization of health care products -- Radiation sterilization -- Substantiation of 25 kGy as a sterilization dose for small or infrequent production batches | ||||
ISO 4909:2000 | Bank cards -- Magnetic stripe data content for track 3 | ||||
ISO 6316:2000 | Hot-rolled steel strip of structural quality | ||||
ISO/IEC 7501-1:1997 | Identification cards -- Machine readable travel documents -- Part 1: Machine readable passport | ||||
ISO 14937:2009 | 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/TS 15843:2000 | Sterilization of health care products -- Radiation sterilization -- Product families and sampling plans for verification dose experiments and sterilization dose audits, and frequency of sterilization dose audits | ||||
ISO/FDIS 17664 | Processing of health care products -- Information to be provided by the medical device manufacturer for the processing of medical devices | ||||
ISO/CD 16342 | Sterilization of health care products -- Biological indicators -- Method for validation of a biological indicator incubation period | ||||
ISO 17664:2004 | Sterilization of medical devices -- Information to be provided by the manufacturer for the processing of resterilizable medical devices | ||||
ISO 15882:2003 | Sterilization of health care products -- Chemical indicators -- Guidance for selection, use and interpretation of results |
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