11.080.20 消毒剂和防腐剂 标准查询与下载
共找到 273 条与 消毒剂和防腐剂 相关的标准，共 19 页
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
- ICS
- 11.080.20
- CCS
- 发布
- 2012-09-17
- 实施
- 2012-09-17
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); German version prEN ISO 11135:2012
- ICS
- 11.080.20
- CCS
- C47
- 发布
- 2012-09-01
- 实施
DIN EN ISO 11140-1:2012 医疗保健产品灭菌. 化学指示剂. 第1部分:一般要求 (ISO/DIS 11140-1-2012); 德文版本prEN ISO 11140-1-2012
Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO/DIS 11140-1:2012); German version prEN ISO 11140-1:2012
- ICS
- 11.080.20
- CCS
- C42
- 发布
- 2012-09
- 实施
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1); German version EN 13727:2012
- ICS
- 11.080.20
- CCS
- C12
- 发布
- 2012-07
- 实施
This European Standard specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water, or - in the case of
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
- ICS
- 11.080.20
- CCS
- 发布
- 2012-06-22
- 实施
- 2012-06-22
This European Standard specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water, or-in the case of ready-to-use products-with water. Products can only be tested at a concentration of 80 % or less (97 % with a modified method for special cases) as some dilution is always produced by adding the test organisms and interfering substance. This European Standard applies to products that are used in the medical area in the fields of hygienic handrub, hygienic handwash, surgical handrub, surgical handwash, instrument disinfection by immersion, and surface disinfection by wiping, spraying, flooding or other means. This European Standard applies to areas and situations where disinfection or antisepsis is medically indicated. Such indications occur in patient care, for example: in hospitals, in community medical facilities and in dental institutions; in clinics of schools, of kindergartens and of nursing homes; and may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patients. NOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2 This method corresponds to a phase 2 step 1 test. NOTE 3 This method cannot be used to evaluate the activity of products against Legionella in watersystems against mycobacteria and against bacterial spores. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations".
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1) (incorporates Amendment A1: 2013)
- ICS
- 11.080.20
- CCS
- 发布
- 2012-05-01
- 实施
Automatic Potentiometric Titration Method for Determination of Active Components in Chemical Disinfectants
- ICS
- 11.080.20
- CCS
- C 47
- 发布
- 2012-01-12
- 实施
- 2012-06-01
This International Standard specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid chemical sterilizing agents of single-use medical devices comprising, in whole or in part, materials of animal origin.
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 pr
- ICS
- 11.080.20
- CCS
- C05
- 发布
- 2011-10
- 实施
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 pr
- ICS
- 11.080.20
- CCS
- C47
- 发布
- 2011-08-01
- 实施
- 2011-08-27
This International Standard specifies requirements for the characterization of a liquid chemical sterilizing agent and for the development, validation, process control and monitoring of sterilization by liquid chemical sterilizing agents of single-use medical devices comprising, in whole or in part, materials of animal origin.This International Standard covers the control of risks arising from contamination with bacteria and fungi by application of a liquid chemical sterilization process. Risks associated with other microorganisms can be assessed using other methods (see Note 1).This International Standard is not applicable to material of human origin. This
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 pr
- ICS
- 11.080.20
- CCS
- 发布
- 2011-07-01
- 实施
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 pr
- ICS
- 11.080.20
- CCS
- C47
- 发布
- 2011-07
- 实施
Sterilization of health care products. Chemical indicators. Part 4. Class 2 indicators for steam penetration test packs
- ICS
- 11.080.20
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Sterilization of health care products. Chemical indicators. Part 2. Test equipment and methods
- ICS
- 11.080.20
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Specifies requirements for the development, validation, process control and monitoring of the sterilization, by the use of liquid chemical sterilants, of single-use medical devices comprising, in whole or in part, materials of animal origin.
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 pr
- ICS
- 11.080.20
- CCS
- C47
- 发布
- 2011
- 实施
Sterilization of health care products. Chemical indicators. Part 5. Class 2 indicators for air removal test sheets and packs
- ICS
- 11.080.20
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Sterilization of care products. Chemical indicators. Part 3. Class 2 indicators for steam penetration test sheets
- ICS
- 11.080.20
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Sterilization of health care products. Chemical indicators. Part 1. General requirements
- ICS
- 11.080.20
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Sterilization of health care products - Chemical indicators - Guidance for selection, use and interpretation of results.
- ICS
- 11.080.20
- CCS
- C04;G65
- 发布
- 2010-04-01
- 实施
- 2010-04-03
The procedure in this test method should be used to evaluate the activity of the test formulation in reducing the bacterial population of the hands immediately after a single use and to determine persistent activity (inhibition of growth) after 6 h. Optionally, measurements of persistent activity after a 3 h period and measurements of cumulative activity may be made after repetitive uses over a five day period.1.1 This test method is designed to measure the reduction of microbial flora on the skin. It is intended for determining both immediate and persistent (continuing antimicrobial effect) microbial reductions, after single or repetitive treatments, or both. It may also be used to measure cumulative antimicrobial activity after repetitive treatments. 1.2 A knowledge of microbiological techniques is required for these procedures. 1.3 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects (21 CFR, Parts 50 and 56) 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.4.1 In this test method, SI units are used for all applications, except for distance, in which case inches are used and SI units follow in parentheses. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
Standard Test Method for Evaluation of Surgical Hand Scrub Formulations
- ICS
- 11.080.20
- CCS
- 发布
- 2010-04-01
- 实施
