AAMI ST50-2004/(R)2018
Dry Heat (Heated Air) Sterilizers
干热（热空气）灭菌器
2004-04-07
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
JB/T 20163-2014
药用干热灭菌器
Pharmaceutical dry heating sterilizer
2014-07-09
CID A-A-50899
STERILIZER, DRY HEAT (NO S/S DOCUMENT)
干热灭菌器（无S/S文件）
1985-12-30
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
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
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/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
KS M 6895
구두용 가죽의 내건열성 시험 방법
鞋类结构的空气干皮革的耐热性试验方法
2016-12-19
NB/T 10156-2019
空气源热泵干燥机组通用技术规范
General technical specifications for air source heat pump drying unit
2019-06-04
KS M 6895(2021 Confirm)
구두용 가죽의 내건열성 시험 방법
鞋类结构风干皮革耐热性试验方法
2016-12-19