医疗器械消毒剂检测

GB 27949-2020 医疗器械消毒剂通用要求

General requirements of disinfectant of medical instruments

GB/T 27949-2011 医疗器械消毒剂卫生要求

本标准规定了医疗器械消毒剂的技术要求、试验方法、使用方法、标志、标签和说明书及注意事项。 本标准适用于医疗器械消毒、灭菌用消毒剂。 本标准不适用于带消毒因子发生装置的消毒器械及气体类或在特定条件下气化后发挥作用的消毒、灭菌产品

Hygienic requirements for medical items disinfection

GB 27949-2011 医疗器械消毒剂通用要求

ISO 14937:2000/Cor 1:2003 医疗保健产品.医疗器械用消毒剂的特性和消毒方法的开发、验证和常规控制的一般要求.技术勘误1

This is Technical Corrigendum 1 to ISO 14937-2000 (Sterilization of health care products — General requirements for characterization of a sterilizing

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; Technical Corrigendum 1

SANS 1593:1994 医疗器械用戊二醛制消毒剂

Specifies requirements for 2 types of disinfectant based on glutaraldehyde and intended for use on medical instruments

Disinfectants based on glutaraldehyde for use on medical instruments

KS P ISO 14937:2012 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的通用要求

이 표준은 의료기기용 멸균제의 특징과 멸균 공정의 개발, 밸리데이션 및 정기 모니터링에 대

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 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求

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

BS EN ISO 14937:2010 保健产品灭菌 医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的一般要求

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

BS EN ISO 14937:2009 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的一般要求

1.1.1 This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation

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

EN ISO 14937:2009 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求

This International Standard specifies general requirements for the characterization of a sterilizingagent and for the development, validation

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)

DIN EN ISO 14937:2010 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求 (ISO 14937-2009); 德文版本 EN ISO 14937-2009

This Standard specifies general requirements for the characterization of a sterilizing agent, and for the development, validation, and routine

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); German version EN ISO 14937:2009

BS EN 13727:2003 化学消毒剂和防腐剂.医疗器械用化学消毒剂杀菌活性评价的定量悬浮试验.试验方法和要求(第2阶段/第1步)

This European Standard specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant products that form

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (Phase 2/Step 1)

NF T72-600:2013 化学消毒剂和抗菌剂.医疗器械用化学消毒剂的杀菌活性评价用定量悬浮试验.试验方法和要求(第2阶段,第1步)

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)

BS EN 13624:2013 化学消毒剂与防腐剂.医疗器械用化学消毒剂杀真菌能力评价用定量悬浮液试验.试验方法和要求(第2阶段第1步)

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)

BS EN 13624:2021 化学消毒剂与防腐剂.医疗器械用化学消毒剂杀真菌能力评价用定量悬浮液试验.试验方法和要求(第2阶段第1步)

This European Standard specifies a test method and the minimum requirements for fungicidal or yeasticidal activity of chemical disinfectant products

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)

GB 27949-2020 医疗器械消毒剂通用要求

General requirements of disinfectant of medical instruments

GB/T 27949-2011 医疗器械消毒剂卫生要求

本标准规定了医疗器械消毒剂的技术要求、试验方法、使用方法、标志、标签和说明书及注意事项。 本标准适用于医疗器械消毒、灭菌用消毒剂。 本标准不适用于带消毒因子发生装置的消毒器械及气体类或在特定条件下气化后发挥作用的消毒、灭菌产品

Hygienic requirements for medical items disinfection

GB 27949-2011 医疗器械消毒剂通用要求

ISO 14937:2000/Cor 1:2003 医疗保健产品.医疗器械用消毒剂的特性和消毒方法的开发、验证和常规控制的一般要求.技术勘误1

This is Technical Corrigendum 1 to ISO 14937-2000 (Sterilization of health care products — General requirements for characterization of a sterilizing

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; Technical Corrigendum 1

SANS 1593:1994 医疗器械用戊二醛制消毒剂

Specifies requirements for 2 types of disinfectant based on glutaraldehyde and intended for use on medical instruments

Disinfectants based on glutaraldehyde for use on medical instruments

KS P ISO 14937:2012 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的通用要求

이 표준은 의료기기용 멸균제의 특징과 멸균 공정의 개발, 밸리데이션 및 정기 모니터링에 대

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 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求

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

BS EN ISO 14937:2010 保健产品灭菌 医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的一般要求

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

BS EN ISO 14937:2009 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发、验证及常规控制的一般要求

1.1.1 This International Standard specifies general requirements for the characterization of a sterilizing agent and for the development, validation

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

EN ISO 14937:2009 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求

This International Standard specifies general requirements for the characterization of a sterilizingagent and for the development, validation

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)

DIN EN ISO 14937:2010 保健产品灭菌.医疗器械用消毒剂的特性和消毒方法的研发,验证及常规控制的一般要求 (ISO 14937-2009); 德文版本 EN ISO 14937-2009

This Standard specifies general requirements for the characterization of a sterilizing agent, and for the development, validation, and routine

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); German version EN ISO 14937:2009

BS EN 13727:2003 化学消毒剂和防腐剂.医疗器械用化学消毒剂杀菌活性评价的定量悬浮试验.试验方法和要求(第2阶段/第1步)

This European Standard specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant products that form

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (Phase 2/Step 1)

NF T72-600:2013 化学消毒剂和抗菌剂.医疗器械用化学消毒剂的杀菌活性评价用定量悬浮试验.试验方法和要求(第2阶段,第1步)

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)

BS EN 13624:2013 化学消毒剂与防腐剂.医疗器械用化学消毒剂杀真菌能力评价用定量悬浮液试验.试验方法和要求(第2阶段第1步)

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)

BS EN 13624:2021 化学消毒剂与防腐剂.医疗器械用化学消毒剂杀真菌能力评价用定量悬浮液试验.试验方法和要求(第2阶段第1步)

This European Standard specifies a test method and the minimum requirements for fungicidal or yeasticidal activity of chemical disinfectant products

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)