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Dry Heat Sterilizer

Dry Heat Sterilizer, Total:128 items.

In the international standard classification, Dry Heat Sterilizer involves: Pharmaceutics, Sterilization and disinfection, Environmental testing, Geology. Meteorology. Hydrology.


Professional Standard - Machinery, Dry Heat Sterilizer

American National Standards Institute (ANSI), Dry Heat Sterilizer

  • ANSI/AAMI ST50-2004 Dry heat (heated air) sterilizers
  • ANSI/AAMI ST40-2004 Table-top dry heat (heated air) sterilization and sterility assurance in health care facilities
  • ANSI/AAMI/ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • ANSI/AAMI ST25-1987 Guideline for Industrial Moist Heat Sterilization of Medical Products
  • ANSI/AAMI/ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • ANSI/AAMI/ISO 20857:2010 Sterilization of health care products - Dry heat: Requirements for the development, validation and routine control of an industrial sterilization process for medical devices

Professional Standard - Medicine, Dry Heat Sterilizer

  • YY 1275-2016 Dry heat (heated air) sterilizers
  • YY 0217.3-1995 Tunnel Sterilization Dryer
  • YY/T 1263-2015 Evaluation of materials of medical device subject to dry heat sterilization
  • YY/T 1276-2016 Requirements for the development, validation and routine control of dry heat sterilization process for medical devices
  • YY 1276-2016 Requirements for development, validation and routine control of dry heat sterilization process for medical devices
  • YY/T 1265-2015 Evaluation of materials of medical device subject to moist heat sterilization

British Standards Institution (BSI), Dry Heat Sterilizer

  • BS EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Biological indicators for dry heat sterilization processes
  • BS EN ISO 11138-4:2017 Tracked Changes. Sterilization of health care products. Biological indicators. Biological indicators for dry heat sterilization processes
  • BS EN ISO 20857:2013 Sterilization of health care products. Dry heat. Requirements for the development, validation and routine control of a sterilization process for medical devices
  • BS EN ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Biological indicators for moist heat sterilization processes
  • BS EN ISO 11138-3:2009 Sterilization of health care products - Biological indicators - Biological indicators for moist heat sterilization processes
  • BS EN ISO 11138-3:2017 Sterilization of health care products. Biological indicators. Biological indicators for moist heat sterilization processes
  • DD CEN ISO/TS 17665-2:2009 Sterilization of health care products. Moist heat. Guidance on the application of ISO 17665-1
  • BS EN ISO 17665-1:2006 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
  • 22/30409085 DC BS EN ISO 17665. Sterilization of health care products. Moist heat. Requirements for the development, validation and routine control of a sterilization process for medical devices
  • PD ISO/TS 17665-3:2013 Sterilization of health care products. Moist heat. Guidance on the designation of a medical device to a product family and processing category for steam sterilization

Association Francaise de Normalisation, Dry Heat Sterilizer

  • NF EN ISO 11138-4:2017 Stérilisation des produits de santé - Indicateurs biologiques - Partie 4 : indicateurs biologiques pour la stérilisation à la chaleur sèche
  • NF S98-004-4*NF EN ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4 : biological indicators for dry heat sterilization processes
  • NF S98-004-4:2006 Sterilization of health care products - Biological indicators - Part 4 : biological indicators for dry heat sterilization processes.
  • NF S98-104*NF EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
  • NF EN ISO 20857:2013 Stérilisation des produits de santé - Chaleur sèche - Exigences pour l'élaboration, la validation et le contrôle de routine d'un processus de stérilisation pour dispositifs médicaux
  • NF EN ISO 11138-3:2017 Stérilisation des produits de santé - Indicateurs biologiques - Partie 3 : indicateurs biologiques pour la stérilisation à la chaleur humide
  • NF S98-004-3*NF EN ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3 : biological indicators for moist heat sterilization processes
  • NF S98-004-3:2006 Sterilization of health care products - Biological indicators - Part 3 : biological indicators for moist heat sterilization processes.
  • NF EN 868-7:2017 Emballages des dispositifs médicaux stérilisés au stade terminal - Partie 7 : papier enduit d'adhésif pour des procédés de stérilisation à basse température - Exigences et méthodes d'essai
  • NF EN ISO 17665-1:2006 Stérilisation des produits de santé - Chaleur humide - Partie 1 : exigences pour le développement, la validation et le contrôle de routine d'un procédé de stérilisation des dispositifs médicaux
  • NF CEN ISO/TS 17665-2:2009 Stérilisation des produits de santé - Chaleur humide - Partie 2 : directives relatives à l'application de l'ISO 17665-1

European Committee for Standardization (CEN), Dry Heat Sterilizer

  • EN 866-6:1999 Biological Systems for Testing Sterilizers and Sterilization Processes - Part 6: Particular Systems for Use in Dry Heat Sterilizers
  • EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • EN 554:1994 Sterilization of Medical Devices - Validation and Routine Control of Sterilization by Moist Heat
  • EN ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • EN 866-3:1997 Biological Systems for Testing Sterilizers and Sterilization Processes - Part 3: Particular Systems for Use in Moist Heat Sterilizers
  • EN 866-7:1999 Biological Systems for Testing Sterilizers and Sterilization Processes - Part 7: Particular Requirements for Self-Contained Biological Indicator Systems for Use in Moist Heat Sterilizers
  • prEN ISO 17665 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 17665:2022)
  • EN ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes

未注明发布机构, Dry Heat Sterilizer

  • BS EN 866-6:2000 Biological systems for testing sterilizers and sterilization processes - Part 6: Particular systems for use in dry heat sterilizers
  • BS EN 554:1994(1998) Sterilization ofmedical devices — Validation and routine control ofsterilization by moist heat
  • BS EN 866-3:1997 Biological systems for testing sterilizers and sterilization processes Part 3. Particular systems for use in moist heat sterilizers
  • BS EN 866-7:2000 Biological systems for testing sterilizers and sterilization processes - Part 7: Particular requirements for self - contained biological indicator systems for use in moist heat sterilizers
  • BS 2648:1955(2011) Performance requirements for Electrically - heated laboratory drying ovens

Danish Standards Foundation, Dry Heat Sterilizer

  • DS/EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • DS/EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
  • DS/EN ISO 11138-3:2009 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • DS/EN ISO 17665-1:2006 Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
  • DS/CEN ISO/TS 17665-2:2009 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1

German Institute for Standardization, Dry Heat Sterilizer

  • DIN EN ISO 11138-4:2017-07 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2017); German version EN ISO 11138-4:2017
  • DIN EN ISO 20857:2013-08 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010); German version EN ISO 20857:2013
  • DIN EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2006); English version of DIN EN ISO 11138-4:2006-09
  • DIN EN ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2017); German version EN ISO 11138-4:2017
  • DIN EN ISO 11138-3:2017-07 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2017); German version EN ISO 11138-3:2017
  • DIN EN ISO 17665:2022-11 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 17665:2022); German and English version prEN ISO 17665:2022 / Note: Date of is...
  • DIN EN 868-7:2017-05 Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods; German version EN 868-7:2017
  • DIN EN ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006); German version EN ISO 11138-3:2006
  • DIN EN ISO 17665-1:2006-11 Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006); German version EN ISO 17665-1:2006 / Note: To be replaced b...
  • DIN ISO/TS 17665-2:2009-07 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1 (ISO/TS 17665-2:2009); German version CEN ISO/TS 17665-2:2009 / Note: To be replaced by DIN EN ISO 17665 (2022-11).
  • DIN EN ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2017); German version EN ISO 11138-3:2017

UNKNOWN, Dry Heat Sterilizer

  • GB/T 18281.4-2015 Biological Indicators for Sterilization of Healthcare Products Part 4: Biological Indicators for Dry Heat Sterilization
  • GB/T 18281.3-2015 Biological Indicators for Sterilization of Healthcare Products Part 3: Biological Indicators for Moist Heat Sterilization

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, Dry Heat Sterilizer

  • GB 18281.4-2015 Biological indicators for sterilization of healthcare products - Part 4: Biological indicators for dry heat sterilization
  • GB/T 30435-2013 Electric gravity convection and forced ventilation ovens
  • GB 18278-2000 Sterilization of health care products--Requirements for validation and routine control--Industrial moist heat sterilization
  • GB 18281.3-2000 Sterilization of health care products--Biological indicators--Part 3: Biological indicators for moist heat sterilization
  • GB 18281.3-2015 Biological indicators for sterilization of healthcare products - Part 3: Biological indicators for moist heat sterilization
  • GB/T 20367-2006 Sterilization of health care products. Requirement for validation and routine control of moist heat sterilization in health care facilities
  • GB/T 32710.10-2016 Safety requirements for environmental testing and conditioning equipment.Part 10: Electric gravity convection ovens and forced ventilation ovens
  • GB 18278.1-2015 Damp heat for sterilization of healthcare products - Part 1: Requirements for development, validation and routine control of sterilization processes for medical devices

International Organization for Standardization (ISO), Dry Heat Sterilizer

  • ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • ISO 11134:1994 Sterilization of health care products; requirements for validation and routine control; industrial moist heat sterilization
  • ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
  • ISO/DIS 17665 Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
  • ISO 11138-3:2006 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
  • ISO 11138-3:1995 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization
  • ISO/FDIS 17665:2023 Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
  • ISO/TS 17665-3:2013 Sterilization of health care products - Moist heat - Part 3: Guidance on the designation of a medical device to a product family and processing category for steam sterilization

Lithuanian Standards Office , Dry Heat Sterilizer

  • LST EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2006)
  • LST EN ISO 11138-3:2009 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)
  • LST EN ISO 17665-1:2006 Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)

AENOR, Dry Heat Sterilizer

  • UNE-EN ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2017)
  • UNE-EN ISO 20857:2013 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 20857:2010)
  • UNE-EN ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2017)
  • UNE-EN ISO 17665-1:2007 Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)

国家医药管理局, Dry Heat Sterilizer

IN-BIS, Dry Heat Sterilizer

Korean Agency for Technology and Standards (KATS), Dry Heat Sterilizer

  • KS P ISO 11134:2003 Sterilization of health care products-Requirements for validation androutine control-Industrial moist heat sterilization
  • KS P ISO 11134:2008 Sterilization of health care products-Requirements for validation androutine control-Industrial moist heat sterilization
  • KS P ISO 11138-3:2018 Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes
  • KS P ISO 11138-3:2012 Sterilization of health care products-Biological indicators-Part 3:Biological indicators for moist heat sterilization processes
  • KS P ISO 17665-1:2019 Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices

KR-KS, Dry Heat Sterilizer

  • KS P ISO 11134-2003 Sterilization of health care products-Requirements for validation androutine control-Industrial moist heat sterilization
  • KS P ISO 11138-3-2018 Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes
  • KS P ISO 17665-1-2019 Sterilization of health care products — Moist heat — Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices

U.S. Air Force, Dry Heat Sterilizer

Group Standards of the People's Republic of China, Dry Heat Sterilizer

  • T/CQAP 3001-2020 Requirements for parameter release of sterile products sterilized by moist heat
  • T/CASME 325-2023 Testing method for performance of moist heat sterilizer
  • T/CNPPA 3023-2023 Application guide for moist heat sterilization bag for pharmaceutical packaging materials

工业和信息化部, Dry Heat Sterilizer

Professional Standard - Agriculture, Dry Heat Sterilizer

  • 42兽药典 三部-2015 Main content inactivated vaccine Clostridioides disease multi-linked dry powder inactivated vaccine

Taiwan Provincial Standard of the People's Republic of China, Dry Heat Sterilizer

  • CNS 14621-2002 Sterilization of health care products-requirements for validation and routine control-industrial moist heat sterilization
  • CNS 14622-3-2002 Sterilization of health care products-biological indicators-part 3:Biological indicators for moist heat sterilization
  • CNS 14622.3-2002 Sterilization of health care products-biological indicators-part 3:Biological indicators for moist heat sterilization

RU-GOST R, Dry Heat Sterilizer

  • GOST ISO 11138-3-2012 Sterilization of health care products. Biological indicators. Part 3. Biological indicators for moist heat sterilization
  • GOST R ISO 11134-2000 Sterilization of health care products. Requirements for validation and routine control. Industrial moist heat sterilization
  • GOST R ISO 11138-3-2000 Sterilization of health care products. Biological indicators. Part 3. Biological indicators for moist heat sterilization

Professional Standard - Water Conservancy, Dry Heat Sterilizer

工业和信息化部/国家能源局, Dry Heat Sterilizer

National Metrological Technical Specifications of the People's Republic of China, Dry Heat Sterilizer

  • JJF 1308-2011 Calibration Specification for Thermometers of Clinic Autoclave

US-AAMI, Dry Heat Sterilizer

  • ANSI/AAMI/ISO TIR17665-3:2014 Sterilization of health care products - Moist heat - Guidance on the designation of a medical product to a product family and processing category for steam sterilization

国家药品监督管理局, Dry Heat Sterilizer

  • YY/T 1600-2018 Product families and process categories for moist heat sterilization of medical devices

Canadian Standards Association (CSA), Dry Heat Sterilizer

  • CSA ISO 11134-98-CAN/CSA:1998 Sterilization of Health Care Products - Requirements for Validation and Routine Control - Industrial Moist Heat Sterilization First Edition; ISO 11134: 1994; Supersedes CAN/CSA-Z214.4: 1987

PT-IPQ, Dry Heat Sterilizer





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