11.080.20 消毒剂和防腐剂 标准查询与下载

DS/EN 14563:2009 化学消毒剂和防腐剂 用于评价医疗领域仪器用化学消毒剂的分枝杆菌或结核菌活性的定量载体试验 试验方法和要求（第 2 阶段，第 2 步）

This European Standard specifies a test method and the minimum requirements for mycobactericidal or tuberculocidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water, or - in the case of ready-to-use products - with water. This European Standard applies to products that are used in the medical area for disinfecting instruments by immersion - even if they are not covered by the EEC/93/42 Directive on Medical Devices.This European Standard applies to areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:- in hospitals, in c

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)

LST EN 14563-2009 化学消毒剂和防腐剂 用于评价医疗领域仪器用化学消毒剂的分枝杆菌或结核菌活性的定量载体试验 试验方法和要求（第 2 阶段，第 2 步）

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)

NF T72-246*NF EN 14563:2009 化学消毒剂和防腐剂.医疗领域仪器用化学消毒剂的分枝杆菌杀菌活性评估用定量带菌者试验.试验方法和要求(第2阶段/第2步)

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2).

ISO/TS 11135-2:2008/Cor 1:2009 保健产品的消毒.环氧乙烷.第2部分:ISO 11135-1应用指南.技术勘误1

Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1; Technical Corrigendum 1

DIN EN 14563:2009 化学消毒剂和防腐剂.医疗领域中器械用化学消毒剂的分枝杆菌或杀结核菌活性评估用定量带菌体试验.试验方法和要求(第2阶段、第2步)

This European Standard specifies a test method and the minimum requirements for mycobactericidal or tuberculocidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water, or - in the case of ready-to-use products - with water. This European Standard applies to products that are used in the medical area for disinfecting instruments by immersion - even if they are not covered by the EEC/93/42 Directive on Medical Devices. This European Standard applies to areas and situations where disinfection 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, kindergartens and 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. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations". NOTE This method corresponds to a phase 2, step 2 test.

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2);Englis

BS EN ISO 15882:2009 保健产品的消毒 化学指示剂 选择、使用和结果说明用指南

Sterilization of health care products. Chemical indicators. Guidance for selection, use and interpretation of results

ASTM E2011-09 评价全部用手工消除病毒活性的人工洗涤方法和手擦配方的标准试验方法

This test method is designed to evaluate the virus-eliminating activity of hygienic handwash and handrub agents from experimentally-contaminated hands. Such formulations may be further assessed in a clinical trial for their effectiveness in the field. This test method incorporates whole-hand exposure and reflects actual use conditions such as friction during hand decontamination, and also enables alternate product forms such as alcohol- or non-alcohol-based liquids, gels, and foams to be tested according to label directions. It is meant to extend, if required, the results of testing with Test Method E 1838, which gives precise reductions in virus infectivity on a limited area of the hands. It may also serve as an alternative test method when product form is not amenable to testing by Test Method E 1838. This test method is not meant for use with surgical hand scrubs or preoperative skin preparations. Note 28212;Application of viruses on the entire surface of both hands entails a greater risk to the subjects than using fingerpads only. Therefore, greater care is needed to ensure that the hands of the participants are free from any apparent damage. Also, virus preparations must be thoroughly screened for, or documented to be free from, extraneous or adventitious pathogens before use in such tests. 1.1 This test method is designed to evaluate handwash or handrub agents for their ability to reduce viral contamination from hands. Note 18212;A knowledge of virological techniques is required for this test method. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.3 This standard may involve hazardous materials, operations and equipment. 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. The user should consult a reference for laboratory safety recommendations. (3-5)

Standard Test Method for Evaluation of Hygienic Handwash and Handrub Formulations for Virus-Eliminating Activity Using the Entire Hand

GOST R ISO 11140-1-2009 健康医疗产品消毒.化学指示剂.第1部分:一般要求

Sterilization of health care products. Chemical indicators. Part 1. General requirements

GOST R ISO 18472-2009 健康医疗产品消毒.生物和化学指示剂.测试设备

Sterilization of health care products. Biological and chemical indicators. Test equipment

ANSI/AAMI/ISO 14161:2009 保健产品的灭菌.生物指示物.选择、使用和检验结果解释指南

Provides guidance for the selection, use, and interpretation of results from the application of biological indicators in the development, validation, and routine monitoring of sterilization processes.

Sterilization of health care products - Biological indicators - Guidance for the selection, use, and interpretation of results

DIN EN ISO 11140-3 Berichtigung 1:2008 卫生保健产品的灭菌.化学指示剂.第3部分:Bowie和Dick型蒸汽渗透试验用2级指示剂系统

Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test (ISO 11140-3:2007); German version EN ISO 11140-3:2007, Corrigendum to DIN EN ISO 11140-3:2007-07; Ge

NF S98-101-2:2008 卫生保健品的消毒.环氧乙烷.第2部分:ISO 11135-1应用指南

Sterilization of health care products - Ethylene oxide - Part 2 : guidance on the application of ISO 11135-1.

DIN ISO/TS 11135-2:2008 卫生保健品的消毒.环氧乙烷.第2部分:ISO 11135-1应用指南

Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1 (ISO/TS 11135-2:2008); German version CEN ISO/TS 11135-2:2008

DIN EN ISO 11138-1 Berichtigung 1:2008 卫生保健产品的消毒.生物指示剂.第1部分:一般要求.技术勘误DIN EN ISO 11138-1-2006-09

Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2006); German version EN ISO 11138-1:2006, Corrigendum to DIN EN ISO 11138-1:2006-09

ISO/TS 11135-2:2008 卫生保健品的消毒.环氧乙烷.第2部分:ISO 11135-1应用指南

This Technical Specification provides guidance for the requirements in ISO 11135-1:2007. It does not repeat the requirements and is not intended to be used in isolation. The exclusions in ISO 11135-1 apply also to this Technical Specification. For ease of reference, the clause numbering in this Technical Specification corresponds to that in ISO 11135-1:2007. Further guidance for the requirements given in ISO 11135-1 is also included in Annex C of ISO 11135-1:2007 and should be used in conjunction with this Technical Specification. This guidance document is intended for people who have a basic knowledge of the principles of EO sterilization but may need help in determining how to best meet the requirements contained in ISO 11135-1. This document is not intended for people lacking a basic knowledge of the principles of EO sterilization.

Sterilization of health care products - Ethylene oxide - Part 2: Guidance on the application of ISO 11135-1

EN 14563:2008 化学消毒剂和防腐剂.医疗领域中器械用化学消毒剂的分枝杆菌或杀结核菌活性评估用定量带菌体试验的试验方法和要求(第2阶段,第2步)

This European Standard specifies a test method and the minimum requirements for mycobactericidal or tuberculocidal activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water, or-in the case of ready-to-use products-with water.This European Standard applies to products that are used in the medical area for disinfecting instruments by immersion-even if they are not covered by the EEC/93/42 Directive on Medical Devices.This European Standard applies to areas and situations where disinfection 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, kindergartens and 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. EN 14885 specifies in detail the relationship of the various tests to one another and to "use recommendations". NOTEThis method corresponds to a phase 2, step 2 test.

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)

GOST R ISO 11140-5-2008 健康医疗产品消毒.化学指示剂.第5部分:排气试纸和测试包2级显示

Sterilization of health care products. Chemical indicators. Part 5. Class 2 indicators for air removal test sheets and packs

SANS 116:2007 含替代酚醛树脂的液体防腐剂

Specifies requirements for antiseptic liquids containing halogenated phenols (or other substituted phenols) with or without pine oil and an emulsifying agent.

Liquid antiseptics containing substituted phenolics

DIN EN ISO 11140-1 Berichtigung 1:2007 卫生保健产品的灭菌.化学指示剂.第1部分:一般要求.技术勘误DIN EN ISO 11140-1-2006

Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005); German version EN ISO 11140-1:2005, Corrigenda to DIN EN ISO 11140-1:2006-04

DIN EN ISO 11138-5 Berichtigung 1:2007 医疗保健产品灭菌.生物指示器.第5部分:低温蒸汽和甲醛溶液灭菌处理用生物指示器(ISO 11138-5:2006)

Sterilization of health care products - Biological indicators - Part 5: Biological indicators for low-temperature steam and formaldehyde sterilization processes (ISO 11138-5:2006); German version EN ISO 11138-5:2006, Corrigenda to DIN EN ISO 11138-5:2006-