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Centrifuge sterilization method

Centrifuge sterilization method, Total:336 items.

The international standard classification for "Centrifuge sterilization method" includes: Geology. Meteorology. Hydrology , Equipment for processing of minerals , Sterilization and disinfection , Other standards related to nuclear energy , Laboratory medicine , Vibration and shock with respect to human beings , Veterinary medicine , Microbiology of water , Pumps , Ignitability and burning behaviour of materials and products , Internal combustion engines , Aerospace engines and propulsion systems , Sterilization and disinfection in general , Sterilizing equipment , Solid fuels , Education .

The Chinese standard classification for "Centrifuge sterilization method" includes: Hydrology and water conservancy instrument , Separating machinery , Public medical equipment , Medical isotopes , Medical apparatus and devices in general , , Acoustic instrument and seismograph , Animal quarantine, veterinary and epidemic prevention , Grain and oil/fat processing machinery , Other food processing machinery , Plastic profile , Pharmaceutical processing machinery and equipment , Lubricating system , Washing equipment , Basic laboratory equipment , Raw pharmaceutical material processing machinery and equipment , Spacecraft power system , General and microsurgical devices , Medical laboratory equipment , Coal petrography , Sanitation in general , Compressor and fan , Refrigeration equipment , Dedicated processing equipment , Fruit processing and products , Special instruments for teaching .


Professional Standard - Water Conservancy

  • SL 144.5-2008 calibration methods of water environmental detecting instrument and equipment calibration method of centrifuge

General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China

  • GB/T 32309-2015 Hydrogen peroxide low temperature plasma sterilizer
  • GB/T 10870-2001 The methods of performance test for positive displacement & centrifugal water-chilling units and heat pump
  • GB/T 13823.14-1995 for the calibration of vibration and shock pick-ups Primary calibration by centrifuge
  • GB/T 31995-2015 Sterilization of health care products―Radiation―Substantiation of a selected sterilization dose method VDmax
  • GB/T 7779-2005 The model designation of centrifuges
  • GB/T 19973.2-2005 Sterilization of medical devices -- Microbiological methods -- Part 2: Test of sterility performed in the validation of a sterilization process
  • GB 15981-1995 Evaluating method and STANDARD for the efficacy of disinfection and sterilization
  • GB/T 10901-1989 Performance testing for centrifuge
  • GB/T 10895-2004 Centrifuge and separator—Measurement method of mechanical vibration
  • GB/T 10901-2023 Centrifuge—Methods of performance testing
  • GB/T 10901-2005 Methods of Performance testing for centrifuge
  • GB/T 7779-1987 The model designation of centrifuges
  • GB 8600-1988 Inspecting method for sterilizing effect of automated autoclave sterilizer
  • GB/T 30690-2014 Monitoring requirements and evaluation of sterilization effect of small steam sterilizer
  • GB/T 18653-2002 Methods for isolation and identification of campylobactor fetus
  • GB/T 10895-1989 Centrifuger and Separator-Measurement method of mechanical vibration
  • GB/T 8600-1988 Inspecting method for sterilizing effect of automated autoclave sterilizer

国家市场监督管理总局、中国国家标准化管理委员会

  • GB/T 7779-2018 Centrifuge—Model designation
  • GB/T 37206-2018 Test method for antibacterial properties of organic separation membrane
  • GB/T 15981-2021 Evaluating method for the efficacy of sterilization for disinfection equipment

Professional Standard - Light Industry

Jilin Provincial Standard of the People's Republic of China

Group Standards of the People's Republic of China

  • T/CAMDI 057-2020 Standard Guide for Writing a Specification for Sterilizable Peel Pouches
  • T/FDSA 003-2019 Test method of the process challenge device(PCD)during low-temperature plasma of hydrogen peroxide
  • T/CAQI 230-2021 Magnetic levitation centrifugal chiller technical requirements and test methods
  • T/CPMA 009-2020 Isolation and identification of Escherichia albertii
  • T/CXDYJ 0004-2020 Pasteurized Organic yak milk,sterilized Organic yak milk
  • T/CAMS 57-2021 Energy efficiency test method for laboratory equipment—Centrifuges
  • T/CASME 325-2023 Testing method for performance of moist heat sterilizer
  • T/CSPSTC 48-2020 Indoor plasma air sanitization device
  • T/WSJD 9-2020 Technical guidelines for on-line monitoring of sterilization effect of small pressure steam sterilizers in medical institutions

未注明发布机构

  • ANSI/AAMI/ISO TIR13004:2013(2016) Technical Information Report Sterilization of health care products—Radiation— Substantiation of a selected sterilization dose: Method VDmax SD
  • DIN CEN ISO/TS 13004:2014*DIN SPEC 13223:2014 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VD<(Index)max><(hoch)SD>
  • DIN EN 1422:2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • ANSI/AAMI/ISO 11737-2:2019 Sterilization of medical devices—Microbiological methods—Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • DIN EN 1422 E:2013-01 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • DIN EN 868-6 E:2015-08 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
  • CSA ISO 11737-2:2021 Sterilization of health care products — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process

Hunan Provincial Standard of the People's Republic of China

Professional Standard - Machinery

Professional Standard - Aerospace

  • QJ 1137A-2005 Centrifugal test method for solid rocket motor
  • QJ 1137-1987 Tactical Missile Solid Rocket Motor Centrifugal Test Method
  • QJ 3307-2008 Centrifugal Static Test Method for Solid Rocket Motor

Professional Standard - Agriculture

Professional Standard - Medicine

  • YY 0217.3-1995 Tunnel sterilizing dryer
  • YY/T 0698.2-2009 Packaging materials for terminal sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • YY/T 0698.8-2009 Packaging materials for terminally sterilized medical devices—Part 8:Re-usable sterilization containers for steam sterilizers—Requirements and test methods
  • YY/T 0698.6-2009 Packaging materials for terminal sterilized medical devices - Part 6: Paper for manufacture of sterile barrier systems intended for sterilization by low temperature sterilization pro
  • YY/T 0657-2008 Medical centrifuge
  • YY/T 0657-2017 Medical centrifuge

国家食品药品监督管理局

  • YY/T 1612-2018 Quality test method of steam in medical sterilization process
  • YY/T 1608-2018 Radiation sterilization of medical device—Sampling method for verification dose experiments and sterilization dose audits
  • YY/T 1607-2018 Radiation sterilization of medical device—Method of dose setting

Professional Standard - Nuclear Industry

  • EJ/T 1243-2017 Radiation sterilization of Medical Devices--Analysis method on Bioburden Data for the Purpose of Validation for Sterilization Dose

Professional Standard - Railway

  • TB/T 2384-1993 Test methods for centrifugal cooling water pumps for diesel locomotives

Professional Standard - Coal

中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会

  • GB/T 33419-2016 Test method of biological indicator for ethylene oxide sterilization processes
  • GB/T 19973.2-2018 Sterilization of medical devices—Microbiological methods—Part 2: Tests of sterility performed in the definition,validation and maintenance of a sterilization process
  • GB/T 33418-2016 Test method of chemical indicator for ethylene oxide sterilization processes
  • GB/T 33420-2016 Evaluation standard of biological for moist heat sterilization processes

Professional Standard - Electron

  • SJ/T 31239-1994 Requirements of Readiness and Methods of Inspection and Assessment for Centrifugal Spray Granulators
  • SJ/T 31441-1994 Requirements of Readiness and Methods of Inspection and Assessment for Centrifugal Refrigerating Units
  • SJ/T 31062-1994 Requirements of readiness and methods of inspection and assessment for RD4500 hydroextractors
  • SJ/T 31404-1994 Requirements of Readiness and Methods of Inspection and Assessment for Centrifugal Blowers

国家药监局

  • YY/T 0698.2-2022 Packaging materials for final sterilized medical devices-Part 2: Requirements and test methods for sterilized packaging materials

国家医药管理局

Professional Standard - Commodity Inspection

  • SN/T 1086-2002 Procedure of isolation and identification for camplylobactor fetus
  • SN 0191-1993 Method for determination of folpet residues in fruits for export

National Health Commission of the People's Republic of China

  • GBT 33418-2016 Test method for ethylene oxide sterilization chemical indicator

Professional Standard - Education

Professional Standard - Farm Machinery

  • NJ 420-1986 Test method for small disc centrifugal milk separator

Taiwan Provincial Standard of the People's Republic of China

  • CNS 14621-2002 Sterilization of health care products-requirements for validation and routine control-industrial moist heat sterilization

American National Standards Institute (ANSI)

  • AAMI TIR27:2001 Sterilization of health care products-Radiation sterilization-Substantiation of 25 kGy as a sterilization dose- Method VDmax
  • AAMI TIR33:2005 Sterilization of health care products - Radiation - Substantiation of a selected sterilization dose - Method VDmax
  • AAMI TIR35:2006 Sterilization of health care products - Radiation sterilization - Alternative sampling plans for verification dose experiments and sterilization dose audits
  • ANSI/ASHRAE 225-2020 ANSI/ASHRAE Standard 225-2020 Method for Performance Testing Centrifugal Refrigerant Compressors and Condensing Units
  • ANSI/AAMI/ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process

SCC

  • UNE 34809:1985 STERILIZED MILK. CONTROL METHOD.
  • DANSK DS/CEN ISO/TS 13004:2014 Sterilization of health care products – Radiation – Substantiation of selected sterilization dose: Method VDmaxSD
  • AENOR UNE-EN 1422:2014 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • NS-EN 1422:1997+A1:2009 Sterilizers for medical purposes — Ethylene oxide sterilizers — Requirements and test methods
  • UNE-EN 1422:1998+A1:2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • DANSK DS/EN 1422:2014 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • NS-EN 1422:2014 Sterilizers for medical purposes — Ethylene oxide sterilizers — Requirements and test methods
  • UNE-EN 1422:1998 STERILIZERS FOR MEDICAL PURPOSES. ETHYLENE OXIDE STERILIZERS. REQUIREMENTS AND TEST METHODS.
  • AENOR UNE-EN 1422+A1:2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • BS EN ISO 11737-2:2000 Sterilization of medical devices. Microbiological methods-Tests of sterility performed in the validation of a sterilization process
  • SPC GB/T 37206-2018 Test method for antibacterial properties of organic separation membrane (TEXT OF DOCUMENT IS IN CHINESE)
  • DIN EN 1422 E:2013 Draft Document - Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods; German version prEN 1422:2012
  • 11/30252448 DC BS EN 1422. Sterilizers for medical purposes. Ethylene oxide sterilizers. Requirements and test methods
  • AWWA PATH50777 Inactivation of Legionella pneumophila by Free Chlorine
  • AAMI/ISO 13004:2022 Sterilization of health care products—Radiation—Substantiation of selected sterilization dose: Method VDmaxSD
  • DANSK DS/ISO 13004:2022 Sterilization of health care products – Radiation – Substantiation of selected sterilization dose: Method VDmaxSD
  • NS-EN 868-2:2009 Packaging for terminally sterilized medical devices — Part 2: Sterilization wrap — Requirements and test methods
  • DIN CEN ISO/TS 13004:2014 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDₘₐₓSD (ISO/TS 13004:2013); German version CEN ISO/TS 13004:2014
  • SN-CEN ISO/TS 13004:2014 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013)
  • DANSK DS/ISO/TS 22421:2021 Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • NS-EN 868-2:2017 Packaging for terminally sterilized medical devices — Part 2: Sterilization wrap — Requirements and test methods
  • UNE-EN 868-2:2009 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • NS-EN ISO 13004:2023 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO 13004:2022)
  • DIN EN ISO 13004 E:2023 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDₘₐₓSD (ISO 13004:2022); German version EN ISO 13004:2023
  • DANSK DS/EN ISO 13004:2023 Sterilization of health care products – Radiation – Substantiation of selected sterilization dose: Method VDmaxSD (ISO 13004:2022)
  • DANSK DS/EN 868-2:2017 Packaging for terminally sterilized medical devices – Part 2: Sterilization wrap – Requirements and test methods
  • NS-EN 1422:1997 Sterilizers for medical purposes — Ethylene oxide sterilizers — Requirements and test methods (Corrigendum AC:2002 incorporated)
  • NS-EN 868-6:2009 Packaging for terminally sterilized medical devices — Part 6: Paper for low temperature sterilization processes — Requirements and test methods
  • UNE-EN ISO 11737-2:2000 STERILIZATION OF MEDICAL DEVICES. MICROBIOLOGICAL METHODS. PART 2: TESTS OF STERILITY PERFORMED IN THE VALIDATION OF A STERILIZATION PROCESS. (ISO 11737-2:1998)
  • NS-EN 868-8:2009 Packaging for terminally sterilized medical devices — Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 — Requirements and test methods
  • AAMI TIR76:2021 Sterilization of health care products - Radiation - Substantiation of a selected sterilization dose at a specified sterility assurance level: Method Vdmax SD-S
  • NS-EN ISO 11737-2:2000 Sterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the validation of a sterilization process (ISO 11737-2:1998)
  • 07/30157769 DC BS EN ISO 11737-2. Sterilization of medical devices. Microbiological methods. Part 2. Tests of sterility performed in the validation of a sterilization process
  • DIN EN 868-2 E:2015 Draft Document - Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods; German and English version prEN 868-2:2015
  • UNE-EN 868-6:2009 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
  • AAMI ST46-2002 Steam sterilization and sterility assurance in health care facilities
  • DANSK DS/EN 868-6:2017 Packaging for terminally sterilized medical devices – Part 6: Paper for low temperature sterilization processes – Requirements and test methods
  • NS-EN 868-6:2017 Packaging for terminally sterilized medical devices — Part 6: Paper for low temperature sterilization processes — Requirements and test methods
  • DANSK DS/EN 868-8:2019 Packaging for terminally sterilized medical devices – Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 – Requirements and test methods
  • BS 767:1951 Hydro-extractors & centrifugal machines
  • NS-EN 868-8:2018 Packaging for terminally sterilized medical devices — Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 — Requirements and test methods
  • AENOR UNE-EN 868-8:2009 Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • DIN EN 868-8 E:2017 Draft Document - Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods; German and English version prEN 868-8:2017
  • DANSK DS/ISO 11737-2:2020 Sterilization of medical devices – Microbiological methods – Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • 07/30166924 DC BS EN 868-2. Packaging materials for terminally sterilized medical devices. Part 2. Sterilization wrap. Requirements and test methods
  • 07/30166936 DC BS EN 868-6. Packaging materials for terminally sterilized medical devices. Part 6. Paper for the manufacture of sterile barrier systems intended for sterilization by low temperature sterilization processes or irradiation. Requirements and test methods
  • NS-EN 868-2:1999 Packaging materials and systems for medical devices which are to be sterilized — Part 2: Sterilization wrap — Requirements and test methods
  • AWWA WQTC60777 Water Quality Effects on the Inactivation Kinetics of MS2 Phage with Free Chlorine
  • UNE-EN 868-2:2000 PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 2: STERILIZATION WRAP. REQUIREMENTS AND TEST METHODS.
  • AENOR UNE-EN 868-2:2017 Packaging materials for sterilized health products in their final phase. Part 2: Wrapping for sterilization. Requirements and test methods.
  • NS-EN 868-7:2009 Packaging for terminally sterilized medical devices — Part 7: Adhesive coated paper for low temperature sterilization processes — Requirements and test methods
  • 07/30167330 DC BS EN 868-8. Packaging materials for terminally sterilized medical devices. Part 8. Re-usable sterilization containers for steam sterilizers conforming to EN 285. Requirements and test methods
  • AAMI ST79:2006 Comprehensive guide to steam sterilization and sterility assurance in health care facilities
  • NS-EN 868-8:1999 Packaging materials and systems for medical devices which are to be sterilized — Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 — Requirements and test methods
  • UNE-EN 868-8:2000 PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 8: RE-USABLE STERILIZATION CONTAINERS FOR STEAM STERILIZERS CONFORMING TO EN 285. REQUIREMENTS AND TEST METHODS.
  • BS ISO 13318-2:2001 Determination of particle size distribution by centrifugal liquid sedimentation methods-Photocentrifuge method

ES-AENOR

BE-NBN

  • NBN 394-1955 Acceptance test of fire extinguishing centrifugal separation pump

British Standards Institution (BSI)

  • BS EN 1422:1998 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • BS EN 1422+A1:1998 Sterilizers for medical purposes. Ethylene oxide sterilizers. Requirements and test methods
  • BS ISO 13004:2022 Sterilization of health care products. Radiation. Substantiation of selected sterilization dose: Method VDmaxSD
  • BS EN ISO 13004:2023 Sterilization of health care products. Radiation. Substantiation of selected sterilization dose. Method VDmaxSD
  • BS EN 868-2:2009 Packaging for terminally sterilized medical devices - Sterilization wrap - Requirements and test methods
  • BS EN 868-2:2017 Packaging for terminally sterilized medical devices. Sterilization wrap. Requirements and test methods
  • PD ISO/TS 22421:2021 Sterilization of health care products. Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • BS 2646-5:1993(2011) Autoclaves for sterilization in laboratories — Part 5 : Methods of test for function and performance
  • BS EN 868-8:2018 Packaging for terminally sterilized medical devices. Re-usable sterilization containers for steam sterilizers conforming to EN 285. Requirements and test methods
  • BS ISO 11737-3:2023 Sterilization of health care products. Microbiological methods. Bacterial endotoxin testing
  • BS 6734:2004 Antimicrobial efficacy of disinfectants for veterinary and agricultural use - Method
  • BS EN 868-6:2009 Packaging for terminally sterilized medical devices - Paper for low temperature sterilization processes - Requirements and test methods
  • BS EN 868-8:2009 Packaging for terminally sterilized medical devices - Re-usable sterilization containers for steam sterilizers conforming to EN 285: Requirements and test methods
  • BS EN 868-6:2017 Packaging for terminally sterilized medical devices. Paper for low temperature sterilization processes. Requirements and test methods
  • 24/30479649 DC BS EN 868-2 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • BS ISO 16063-17:2016 Methods for the calibration of vibration and shock transducers. Primary calibration by centrifuge

German Institute for Standardization

  • DIN EN 1422:2014-08 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods; German version EN 1422:2014
  • DIN EN ISO 13004:2023-03 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VD<(Index)max><(hoch)SD> (ISO 13004:2022); German and English version prEN ISO 13004:2023 / Note: Date of issue 2023-02-10*Intended as...
  • DIN EN ISO 13004:2023 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VD (ISO 13004:2022); German and English version prEN ISO 13004:2023
  • DIN EN 868-2:2017-05 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods; German version EN 868-2:2017
  • DIN EN 1422:2014 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods; German version EN 1422:2014
  • DIN CEN ISO/TS 13004:2014-10*DIN SPEC 13223:2014-10 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VD<(Index)max><(hoch)SD> (ISO/TS 13004:2013); German version CEN ISO/TS 13004:2014
  • DIN 58970-2:1982 Laboratory centrifuges; centrifuge tubes for relative centrifugal acceleration up to 4000
  • DIN EN 868-6:2017-05 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods; German version EN 868-6:2017
  • DIN EN 868-8:2019-03 Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods; German version EN 868-8:2018
  • DIN EN 868-8:2019 Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • DIN EN ISO 11737-2:2020-07 Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019); German version EN ISO 11737-2:2020

Association Francaise de Normalisation

  • NF S63-125:1990 Fire fighting equipment. Centrifugal pum. Tests.
  • NF EN 1422:2014 Stérilisateurs à usage médical - Stérilisateurs à l'oxyde d'éthylène - Exigences et méthodes d'essai
  • NF S98-015/IN1:2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods.
  • NF ISO 13004:2022 Sterilization of health products - Irradiation - Justification of the chosen sterilizing dose: DVmaxD method
  • NF S98-105:1994 Sterilization of medical devices. Validation and routine control of sterilization by moist heat.
  • NF EN 12547:2014 Centrifuges - Common safety requirements
  • NF EN 868-2:2017 Packaging for terminally sterilized medical devices - Part 2: sterilization envelope - Requirements and test methods
  • NF S98-103:1994 Sterilization of medical devices. Validation and routine control of sterilization by irradiation.
  • NF S98-101:1994 Sterilization of medical devices. Validation and routine control of ethylene oxide sterilization.
  • NF S98-051-2*NF EN 868-2:2017 Packaging for terminally sterilized medical devices - Part 2 : sterilization wrap - Requirements and test methods
  • XP ISO/TS 22421:2021 Sterilization of healthcare products - Common requirements for sterilizers used for terminal sterilization of medical devices in healthcare settings
  • NF T72-281:2014 Methods of airborne disinfection of surfaces - Determination of bactericidal, fongicidal, yeasticidal, mycobactericidal, tuberculicidal sporicidal and virucidal activity, including bacteriophages
  • NF S98-051-8:2009 Packaging for terminally sterilized medical devices - Part 8 : re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods.
  • NF EN 868-6:2017 Packaging for terminally sterilized medical devices - Part 6: paper for low temperature sterilization processes - Requirements and test methods
  • NF EN 868-8:2018 Packaging for terminally sterilized medical devices - Part 8: reusable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • NF S98-051-8*NF EN 868-8:2018 Packaging for terminally sterilized medical devices - Part 8 : re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • NF S98-051-6:2009 Packaging materials for terminally sterilized medical devices - Part 6 : paper for low temperature sterilization processes - Requirements and test methods.
  • NF S98-051-6*NF EN 868-6:2017 Packaging for terminally sterilized medical devices - Part 6 : paper for low temperature sterilization processes - Requirements and test methods
  • NF EN ISO 11737-2:2020 Sterilization of health products - Microbiological methods - Part 2: sterility checks carried out during the definition, validation and maintenance of a sterilization process
  • NF S98-118-2*NF EN ISO 11737-2:2020 Sterilization of health care products - Microbiological methods - Part 2 : tests of sterility performed in the definition, validation and maintenance of a sterilization process

Lithuanian Standards Office

  • LST EN 1422-2014 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • LST EN 1422-1997+A1-2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • LST EN 868-2-2009 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • LST EN 868-8-2009 Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • LST EN 868-6-2009 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
  • LST EN 868-7-2009 Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods

US-AAMI

  • ANSI/AAMI/ISO TIR13004:2013 Sterilization of health care products - Radiation - Substantiation of a selected sterilization dose:Method VDmaxSD

Danish Standards Foundation

  • DS/EN 1422+A1:2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • DS/EN 868-2:2009 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • DS/EN 868-8:2009 Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • DS/EN 868-6:2009 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
  • DS/EN ISO 11737-2:2010 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • DS/EN 868-7:2009 Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods

European Committee for Standardization (CEN)

  • EN 1422:2014 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • prEN ISO 13004 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO 13004:2022)
  • EN ISO 11737-2:2020 Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)
  • EN ISO 13004:2023 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO 13004:2022)
  • EN 868-2:2009 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • CEN ISO/TS 13004:2014 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO/TS 13004:2013)
  • EN ISO 11737-2:2000 Sterilization of Medical Devices - Microbiological Methods - Part 2: Tests of Sterility Performed in the Validation of a Sterilization Process ISO 11737-2: 1998
  • EN 1422:1997 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods Incorporates Amendment A1: 2009
  • EN 868-6:2009 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
  • EN 868-6:2017 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods

GSO

  • BH GSO ISO/TS 13004:2022 Sterilization of health care products — Radiation — Substantiation of selected sterilization dose: Method VDmaxSD
  • GSO ISO/TS 13004:2021 Sterilization of health care products — Radiation — Substantiation of selected sterilization dose: Method VDmaxSD
  • BH GSO ISO/TS 22421:2023 Sterilization of health care products — Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • GSO ISO/TS 22421:2023 Sterilization of health care products — Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities
  • GSO 1432:2002 Sanitary appliances — Methods of test for pressurized Flushing devices
  • GSO ISO 11737-2:2015 Sterilization of medical devices -- Microbiological methods -- Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • OS GSO ISO 11737-2:2015 Sterilization of medical devices -- Microbiological methods -- Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • BH GSO ISO 11737-2:2016 Sterilization of medical devices -- Microbiological methods -- Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process

AENOR

  • UNE-EN 1422:2014 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • UNE-EN 868-2:2017 Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods
  • UNE-EN 868-8:2009 Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods
  • UNE-EN 868-6:2017 Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods
  • UNE-EN 868-7:2017 Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods

DIN

  • DIN EN 1422:1997 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods
  • DIN EN 868-2:1999 Packaging materials and systems for medical devices which are to be sterilized - Part 2: Sterilization wrap - Requirements and test methods
  • DIN EN 868-8:1999 Packaging materials and systems for medical devices which are to be sterilized - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods

RU-GOST R

  • GOST R 51563-2000 Liquid centrifugal separators. Safety requirements. Test methods
  • GOST R 57623-2017 Sterilizers for medical purposes. Ethylene oxide sterilizers. Requirements and test methods
  • GOST R 51931-2002 Industrial centrifuges. Safety requirements. Test methods
  • GOST 30425-1997 Canned foods. Method for determination of commercial sterility
  • GOST 31836-2012 Industrial centrifuges. Safety requirements. Test methods
  • GOST 3623-2015 Milk and milk products. Methods for determination of pasteurization
  • GOST 17601-1990 Marine centrifugal separators. Acceptance and methods of tests
  • GOST 13496.6-1971 Mixed feed. Method of detachment of fungi
  • GOST 31827-2012 Liquid centrifugal separators. Safety requirements. Test methods

International Organization for Standardization (ISO)

  • ISO 13004:2022 Sterilization of health care products — Radiation — Substantiation of selected sterilization dose: Method VDmaxSD
  • ISO 11737-2:1998 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the validation of a sterilization process
  • ISO/TS 13004:2013 Sterilization of health care products.Radiation.Substantiation of selected sterilization dose: Method VD<(Index)max><(hoch)SD>
  • ISO 11737-2:2019 Sterilization of health care products — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • ISO/FDIS 11737-3 Sterilization of health care products — Microbiological methods — Part 3: Bacterial endotoxin testing
  • ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • ISO 11737-3:2023 Sterilization of health care products — Microbiological methods — Part 3: Bacterial endotoxin testing

Korean Agency for Technology and Standards (KATS)

CEN - European Committee for Standardization

  • EN ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition@ validation and maintenance of a sterilization process

ES-UNE

  • UNE-EN ISO 13004:2024 Sterilization of health care products - Radiation - Substantiation of selected sterilization dose: Method VDmaxSD (ISO 13004:2022)
  • UNE-EN ISO 11737-2:2020 Sterilization of health care products - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2019)

Indonesia Standards

  • SNI 7461-2008 Testing methods of modified aspalth solubility in toluen using centrifuge tools

American Society for Testing and Materials (ASTM)

  • ASTM E3178-18 Standard Practice for Evaluating Static and Cidal Chemical Decontaminants against Bacillus Spores using Centrifugal Filtration Tubes
  • ASTM D5148-10 Standard Test Method for Centrifuge Kerosine Equivalent
  • ASTM D5148-97(2002) Standard Test Method for Centrifuge Kerosine Equivalent
  • ASTM D5148-97 Standard Test Method for Centrifuge Kerosine Equivalent
  • ASTM D2402-01 Standard Test Method for Water Retention of Textile Fibers (Centrifuge Procedure)
  • ASTM D2402-94 Standard Test Method for Water Retention of Textile Fibers (Centrifuge Procedure)
  • ASTM E1054-08 Standard Test Methods for Evaluation of Inactivators of Antimicrobial Agents
  • ASTM F2559-06 Standard Guide for Writing a Specification for Sterilizable Peel Pouches
  • ASTM D2402-07(2012) Standard Test Method for Water Retention of Textile Fibers (Centrifuge Procedure)
  • ASTM D2402-07 Standard Test Method for Water Retention of Textile Fibers (Centrifuge Procedure)
  • ASTM E1054-08(2013) Standard Test Methods for Evaluation of Inactivators of Antimicrobial Agents
  • ASTM D1290-95(2021) Standard Test Method for Sediment in Water-Emulsion Polishes by Centrifuge

ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc.

US-FCR

International Electrotechnical Commission (IEC)

BR-ABNT

Military Standards (MIL-STD)

Japanese Industrial Standards Committee (JISC)

GOSTR

Malaysia Standards

  • MS 961-1985 Method for testing water and sediment in fuel using centrifuge

PL-PKN

  • PN M71051-1965 Industrial Centrifuges Ranges of sizes of con?inuous filter centrifuges
  • PN M71052-1966 Industrial centrifugesRanges of sizes of batch filter cen?rifuges

KR-KS

  • KS P ISO 11737-2-2018 Sterilization of medical devices — Microbiological methods — Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process
  • KS P ISO 11737-2-2021 Sterilization of health care products — Microbiological methods —Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process

RO-ASRO

  • STAS 7466-1984 CENTRIFUGAL AND AXIAL FANS FOR GENERAL U SE Test methods

IN-BIS

Canadian General Standards Board (CGSB)

PT-IPQ

  • NP EN 868-1-2000 Packaging materials and systems for medical devices which are to be sterilized Part 1:General requirements and test methods

GOST

  • GOST R ISO 11737-2-2022 Sterilization of health care products. Microbiological methods. Part 2. Tests of sterility performed in the definition, validation and maintenance of a sterilization process