11.080.01 消毒和灭菌综合 标准查询与下载
共找到 873 条与 消毒和灭菌综合 相关的标准，共 59 页
This European Standard specifies a laboratory method to determine the leaching behaviour of substances from coatings into water over defined time intervals. The release of substances from coatings under natural conditions cannot be determined withThis method.
Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)
- ICS
- 11.080.01
- CCS
- 发布
- 2011-06-01
- 实施
This European Standard specifies a laboratory method to determine the leaching behaviour of substances from coatings into water over defined time intervals. The release of substances from coatings under natural conditions cannot be determined withThis method.
Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)
- ICS
- 11.080.01
- CCS
- 发布
- 2011-06-01
- 实施
This part of ISO 13408 specifies requirements for, and offers guidance on, equipment, processes,programmes and procedures for the control and validation of lyophilization as an aseptic process. It does notaddress the physical/chemical objectives of a lyophilization process.
Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)
- ICS
- 11.080.01
- CCS
- 发布
- 2011-06-01
- 实施
This European Standard specifies a laboratory method to determine the leaching behaviour of substances from coatings into water over defined time intervals. The release of substances from coatings under natural conditions cannot be determined withThis method.
Aseptic processing of health care products - Part 6: Isolator systems (Incorporates Amendment A1: 2013)
- ICS
- 11.080.01
- CCS
- 发布
- 2011-06-01
- 实施
This European Standard specifies requirements for the development, validation and routine control ofa Low Temperature Steam and Formaldehyde (LTSF) sterilization process for medical devices.
Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices
- ICS
- 11.080.01
- CCS
- 发布
- 2011-06-01
- 实施
This part of ISO 13408 specifies the general requirements for, and offers guidance on, processes,programmes and procedures for development, validation and routine control of the manufacturing process foraseptically-processed health care products.
Aseptic processing of health care products - Part 1: General requirements [Superseded: CEN EN 13824]
- ICS
- 11.080.01
- CCS
- 发布
- 2011-06-01
- 实施
Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (Second Edition)
- ICS
- 11.080.01
- CCS
- 发布
- 2011-01-01
- 实施
Aseptic processing of health care products. Part 4. Clean-in-place technologies
- ICS
- 11.080.01
- CCS
- 发布
- 2011-01-01
- 实施
- 2012-12-01
Sterilization of health care products. Radiation. Part 2. Establishing the sterilization dose
- ICS
- 11.080.01
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Medical products. Radiation sterilization. Dosimetric techniques
- ICS
- 11.080.01
- CCS
- 发布
- 2011
- 实施
- 2012-06-01
Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ICS
- 11.080.01
- CCS
- C47
- 发布
- 2011
- 实施
Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ICS
- 11.080.01
- CCS
- C47
- 发布
- 2011
- 实施
Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ICS
- 11.080.01
- CCS
- C47
- 发布
- 2011
- 实施
Comprehensive guide to steam sterilization and sterility assurance in health care facilities
- ICS
- 11.080.01
- CCS
- C47
- 发布
- 2011
- 实施
Sterilization of medical devices. Requirements for medical devices to be designated «sterile». Part 1. Requirements for terminally sterilized medical devices
- ICS
- 11.080.01
- CCS
- 发布
- 2011
- 实施
- 2013-01-01
Aseptic processing of health care products－Part 2：Filtration
- ICS
- 11.080.01
- CCS
- 发布
- 2010-12-30
- 实施
Aseptic processing of health care products－Part 4：Clean-in-place technologies
- ICS
- 11.080.01
- CCS
- 发布
- 2010-12-30
- 实施
Aseptic processing of healthcare products－Part 5：Sterilization in place
- ICS
- 11.080.01
- CCS
- 发布
- 2010-12-30
- 实施
이 표준은 무균 처리에 의하여 무균 의료용품의 제조에 사용되는 장비의 제품 접촉면에 적용되
Aseptic processing of healthcare products－Part 5：Sterilization in place
- ICS
- 11.080.01
- CCS
- C50
- 发布
- 2010-12-30
- 实施
- 2010-12-30
이 표준은 무균 처리에 의하여 무균 의료용품의 제조에 사용되는 장비의 제품 접촉면에 적용되
Aseptic processing of health care products－Part 4：Clean-in-place technologies
- ICS
- 11.080.01
- CCS
- C50
- 发布
- 2010-12-30
- 实施
- 2010-12-30
