The difference between moist heat sterilization and dry heat sterilization

The difference between moist heat sterilization and dry heat sterilization, Total:173 items.

The international standard classification for "The difference between moist heat sterilization and dry heat sterilization" includes: Sterilizing equipment , Sterilization and disinfection in general , Other standards related to sterilization and disinfection , Pharmaceutics .

The Chinese standard classification for "The difference between moist heat sterilization and dry heat sterilization" includes: Medicinal materials pickoff and Chinese medicine processing machinery , Public medical equipment , Basic standards and general methods , Fire-fighting in general .

Professional Standard - Machinery

JB/T 20119-2009 ot-air circulation sterilzing cabinet
JB/T 20163-2014 Pharmaceutical Dry Heating Sterilizer

Professional Standard - Medicine

YY/T 1263-2015 Evaluation of materials of medical device subject to dry heat sterilization
YY 1275-2016 Dry heat (heated air) sterilizers
YY/T 1265-2015 Evaluation of materials of medical device subject to moist heat sterilization

国家药品监督管理局

YY/T 1600-2018 Product family and processing category for steam sterilization of medical devices

Group Standards of the People's Republic of China

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

Taiwan Provincial Standard of the People's Republic of China

CNS 14622.3-2002 Sterilization of health care products-biological indicators-part 3：Biological indicators for moist heat sterilization
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

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

GB 18278-2000 Sterilization of health care products - Requirements for validation and routine control - Industrial moist heat sterilization
GB 18281.3-2015 Sterilization of health care products―Biological indicators―Part 3:Biological indicators for moist heat sterilization processes
GB 18278.1-2015 Sterilization of health care products―Moist heat―Part 1:Requirements for the development, validation and routine control of a sterilization process for medical devices
GB 18281.3-2000 Sterilization of health care products--Biological indicators--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 18281.4-2015 Sterilization of health care products―Biological indicators―Part 4:Biological indicators for dry heat sterilization processes

未注明发布机构

ANSI/AAMI/ISO 11138-4:2017 Sterilization of health care products—Biological indicators—Part 4: Biological indicators for dry heat sterilization processes
CAN/CSA-ISO 11138-4:2017 Sterilization of health care products — Biological indicators — Part 4: Biological indicators for dry heat sterilization processes
ANSI/AAMI/ISO 11138-3:2017 Sterilization of health care products—Biological indicators—Part 3: Biological indicators for moist heat sterilization processes
CAN/CSA-ISO/TS 17665-3:2017 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
DIN EN ISO 11138-4 E:2014-10 Biological indicators for sterilization of health care products Part 4: Biological indicators for dry heat sterilization processes (draft)
CSA ISO 20857:2019 Sterilization of health care products — Dry heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
ANSI/AAMI/ISO 17665-1:2006(2013) Sterilization of health care products—Moist heat—Part 1: Requirements for the development, validation, and routine control of a sterilization process for medical devices
CAN/CSA-ISO 11138-3:2017 Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes

SCC

AS 2487:1981 Dry heat sterilizers (hot air type)
NS-EN 554:1994 Sterilization of medical devices — Validation and routine control of sterilization by moist heat
UNE-EN 554:1995 STERILIZATION OF MEDICAL DEVICES. VALIDATION AND ROUTINE CONTROL OF STERILIZATION BY MOIST HEAT
CAN/CSA-ISO 11134-1998(R2003) Sterilization of health care products - Requirements for validation and routine control - Industrial moist heat sterilization
NS-EN 866-3:1997 Biological systems for testing sterilizers and sterilization processes — Part 3: Particular systems for use in moist heat sterilizers
UNE-EN 866-3:1997 BIOLOGICAL SYSTEMS FOR TESTING STERILIZERS AND STERILIZATION PROCESSES. PART 3: PARTICULAR SYSTEMS FOR USE IN MOIST HEAT STERILIZERS.
BS 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
NS-EN 866-6:1999 Biological systems for testing sterilizers and sterilization processes — Part 6: Particular systems for use in dry heat sterilizers
UNE-EN 866-6:2001 BIOLOGICAL SYSTEMS FOR TESTING STERILIZERS AND STERILIZATION PROCESSES. PART 6: PARTICULAR SYSTEMS FOR USE IN DRY HEAT STERILIZERS.
AAMI/ISO 11138-3:2017 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes
AAMI/ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
ADA ST40:2004(R2010) Table-top Dry Heat (heated air) Sterilization and Sterility Assurance in Health Care Facilities
DANSK DS/ISO 20857:2010 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
DANSK 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
CAN/CSA-ISO 20857-2019 Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
NS-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
UNE-EN ISO 11138-3:2007 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)
DANSK DS/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)
AENOR 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 11138-3:2009 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)
NS-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)
DANSK DS/EN ISO 17665:2024 Sterilization of health care products – Moist heat – Requirements for the development, validation and routine control of a sterilization process for medical devices
NS-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)
NS-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)
DANSK DS/ISO/TS 17665-3:2014 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
DANSK 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
UNE-EN 866-7:2001 BIOLOGICAL SYSTEMS FOR TESTING STERILIZERS AND STERILIZATION PROCESSES. PART 7: PARTICULAR REQUIREMENTS FOR SELF-CONTAINED BIOLOGICAL INDICATOR SYSTEMS FOR USE IN MOIST HEAT STERILIZERS.
CAN/CSA-Z17665-1-2009(R2014) Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
AAMI ST63:2002 Sterilization of health care products - Requirements for the development, validation, and routine control of an industrial sterilization process for medical devices - Dry heat
NS-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)
DANSK DS/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)
NS-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)
NS-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)
AENOR UNE-EN ISO 11138-4:2017 Sterilization of medical products. Biological indicators. Part 4: Biological indicators for dry heat sterilization processes. (ISO 11138-4:2017).
AENOR 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)
NS-EN ISO 17665:2024 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)
BS 3421:1961 Specification for performance of electrically heated sterilizing ovens
DANSK DS/CEN ISO/TS 17665-2:2009 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1
CAN/CSA-Z17665-2-2009 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1
NS-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)
07/30164697 DC ISO 20857. Sterilization of health care products. Dry heat. Requirements for the development, validation and routine control of an industrial sterilization process for medical devices
UNE-EN ISO 11138-4:2007 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO 11138-4:2006)
DIN EN ISO 11138-3 E:2015 Draft Document - Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO/DIS 11138-3:2015); German and English version prEN ISO 11138-3:2015
BS 3970-5:1968 Sterilizing and disinfecting equipment for medical products-Electrically heated steam generators for use with hospital sterilizers
DIN EN ISO 11138-4 E:2015 Draft Document - Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes (ISO/DIS 11138-4:2015); German and English version prEN ISO 11138-4:2015
AENOR 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)

American National Standards Institute （ANSI)

ANSI/AAMI ST50-2004 Dry heat (heated air) sterilizers
AAMI TIR13:1997 Principles of industrial moist heat sterilization, 1ed
ANSI/AAMI ST25-1987 Guideline for Industrial Moist Heat Sterilization of Medical Products
ANSI/AAMI ST40-2004 Table-top dry heat (heated air) sterilization and sterility assurance in health care facilities
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 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes

British Standards Institution (BSI)

BS EN 554:1994(1998) Sterilization ofmedical devices — Validation and routine control ofsterilization by moist heat
BS EN ISO 11138-4:2017 Sterilization of health care products. Biological indicators. Biological indicators for dry heat sterilization processes
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 866-6:2000 Biological systems for testing sterilizers and sterilization processes - Part 6: Particular systems for use in dry heat sterilizers
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
BS EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Biological indicators for dry 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 17665:2024 Sterilization of health care products. Moist 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 11138-3:2017 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 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 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 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

European Committee for Standardization (CEN)

EN 554:1994 Sterilization of Medical Devices - Validation and Routine Control of Sterilization by Moist Heat
EN 866-3:1997 Biological Systems for Testing Sterilizers and Sterilization Processes - Part 3: Particular Systems for Use in Moist Heat Sterilizers
EN 866-6:1999 Biological Systems for Testing Sterilizers and Sterilization Processes - Part 6: Particular Systems for Use in Dry 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
FprEN 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/FDIS 17665:2023)
EN ISO 11138-4:2017 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
EN ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes

KR-KS

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

Korean Agency for Technology and Standards (KATS)

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 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 11138-3-2023 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

US-AAMI

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

Association Francaise de Normalisation

NF EN ISO 11138-3:2017 Sterilization of healthcare products - Biological indicators - Part 3: biological indicators for moist heat sterilization
NF EN ISO 11138-4:2017 Sterilization of healthcare products - Biological indicators - Part 4: biological indicators for dry heat sterilization
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 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 EN ISO 17665-1:2006 Sterilization of healthcare products - Moist heat - Part 1: requirements for the development, validation and routine control of a medical device sterilization process
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 Sterilization of healthcare products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
NF S98-004-4:2006 Sterilization of health care products - Biological indicators - Part 4 : biological indicators for dry heat sterilization processes.

International Organization for Standardization (ISO)

ISO 11134:1994 Sterilization of health care products; requirements for validation and routine control; industrial 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/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 13683:1997 Sterilization of health care products - Requirements for validation and routine control of moist heat sterilization in health care facilities
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 17665:2024 Sterilization of health care products — Moist heat — Requirements for the development, validation and routine control of a sterilization process for medical devices
ISO 11138-4:2006 Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
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
ISO/TS 17665-2:2009 Sterilization of health care products - Moist heat - Part 2: Guidance on the application of ISO 17665-1

GSO

BH GSO ISO/TS 17665-3:2017 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
GSO ISO/TS 17665-3:2015 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
BH GSO ISO 11138-3:2022 Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes
GSO ISO 11138-3:2021 Sterilization of health care products — Biological indicators — Part 3: Biological indicators for moist heat sterilization processes
BH GSO ISO 11138-4:2022 Sterilization of health care products — Biological indicators — Part 4: Biological indicators for dry heat sterilization processes
GSO ISO 11138-4:2021 Sterilization of health care products — Biological indicators — Part 4: Biological indicators for dry heat sterilization processes
GSO ISO 20857:2016 Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
OS GSO ISO 20857:2016 Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
BH GSO ISO 20857:2017 Sterilization of health care products -- Dry heat -- Requirements for the development, validation and routine control of a sterilization process for medical devices
OS GSO ISO 17665-1:2014 Sterilization of health care products -- Moist heat -- Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
GSO ISO 17665-1:2014 Sterilization of health care products -- Moist heat -- Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices
GSO ISO/TS 17665-2:2015 Sterilization of health care products -- Moist heat -- Part 2: Guidance on the application of ISO 17665-1

RU-GOST R

GOST R ISO 11134-2000 Sterilization of health care products. Requirements for validation and routine control. Industrial moist heat sterilization
GOST ISO 11138-3-2012 Sterilization of health care products. Biological indicators. Part 3. Biological indicators for moist heat sterilization
GOST R ISO 13683-2000 Sterilization of health care products. Requirements for validation and routine control of moist heat sterilization in health care facilities
GOST R ISO 11138-3-2000 Sterilization of health care products. Biological indicators. Part 3. Biological indicators for moist heat sterilization

Danish Standards Foundation

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 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 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

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 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 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 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 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 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 11138-3:2006 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 17665:2024 Sterilization of health care products - Moist heat - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665:2024)
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).

UNKNOWN

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

IN-BIS

IS 3119-1978 Specification for hot air sterilizers

Lithuanian Standards Office

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 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 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

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 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 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)

GOSTR

GOST R 58163-2018 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

Canadian Standards Association (CSA)

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

Others: