AAMI ST50-2004/(R)2018
Dry Heat (Heated Air) Sterilizers
干热（热空气）灭菌器
2004-04-07
YY 1275-2016
热空气型干热灭菌器
Dry heat (heated air) sterilizers
2016-03-23
CID A-A-50899
STERILIZER, DRY HEAT (NO S/S DOCUMENT)
干热灭菌器（无S/S文件）
1985-12-30
ADA ST40-2004(R2010)
Table-top Dry Heat (heated air) Sterilization and Sterility Assurance in Health Care Facilities
医疗设施中的台式干热（热空气）灭菌和无菌保证
DOXPUB 11-0007-SOP
Operation and Maintenance of The Lytzen Class 100 Dry Heat Sterilizer
Lytzen 100型干热灭菌器的使用与维护
2007-08-01
YY/T 1263-2015
适用于干热灭菌的医疗器械的材料评价
Evaluation of materials of medical device subject to dry heat sterilization
2015-03-02
BS EN ISO 11138-4-2017
Sterilization of health care products. Biological indicators-Biological indicators for dry heat sterilization processes
医疗保健产品的消毒 生物指标
2017-04-30
AAMI/ISO 11138-4-2017
Sterilization of health care products - Biological indicators - Part 4: Biological indicators for dry heat sterilization processes
医疗保健产品的灭菌.生物指示剂.第4部分:干热灭菌过程用生物指示剂
2017-08-01
GB 18281.4-2015
医疗保健产品灭菌 生物指示物 第4部分:干热灭菌用生物指示物
Sterilization of health care products—Biological indicators—Part 4:Biological indicators for dry heat sterilization processes
2015-12-10
GOST R ISO 20857-2016
Стерилизация медицинской продукции. Горячий воздух. Требования к разработке, валидации и текущему контролю процесса стерилизации медицинских изделий
医疗器械灭菌干热 对医疗器械灭菌过程的开发 验证和常规控制的要求
ISO 11138-4-2017
Sterilization of health care products — Biological indicators — Part 4: Biological indicators for dry heat sterilization processes
保健产品的灭菌 - 生物指示器 - 第4部分:干热灭菌过程的生物指标
2017-03-03
AAMI/ISO 20857-2010/(R)2015
Sterilization of health care products - Dry heat - Requirements for the development, validation and routine control of a sterilization process for medical devices
医疗保健产品的灭菌.干热.医疗器械灭菌过程的开发、验证和常规控制要求
2010-12-08
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
医疗保健产品的消毒 干热 医疗器械灭菌过程的开发、验证和常规控制要求
2013-04-30
KS P ISO 20857
의료제품의 멸균 — 건열 — 의료기기 대상 멸균 공정의 개발, 유효성 확인, 일상관리의 요구사항
医疗保健产品的灭菌.干热.医疗器械灭菌过程的开发、验证和常规控制要求
2024-12-23
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
保健品灭菌——干热；医疗器械灭菌过程的开发、验证和常规控制要求
2010-08-17
YY/T 1276-2016
医疗器械干热灭菌过程的开发、确认和常规控制要求
Requirements for the development,validation and routine control of dry heat sterilization process for medical devices
2016-03-23
AAMI ST40-2004/(R)2018
Periodic review of ANSI/AAMI ST40:2004, Table-top dry heat (heated air) sterilization and sterility assurance in health care facilities (Reaffirmed 2010)
定期审查ANSI/AAMI ST40:2004《医疗设施中的台式干热（加热空气）灭菌和无菌保证》（2010年重申）
2004-10-07
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)
医疗保健产品的灭菌.生物指示剂.第4部分:干热灭菌过程用生物指示剂（ISO 11138-4-2006）
2007-05-16
BS 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
ISO 20857 医疗保健产品的消毒 干热 医疗器械工业灭菌过程的开发、验证和常规控制要求
2007-04-12
PDA TR 30
Technical Report 30 Revised 2012, (TR 30) Parametric Release of Pharmaceuticals and Medical Device Products Terminally Sterilized by Moist Heat
2012年修订的技术报告30 （TR 30）湿热灭菌药品和医疗器械产品的参数放行
2012-05-01