WS 310.2-2009

医院消毒供应中心 第2部分：清洗消毒及灭菌技术操作规范

Central sterile supply department(CSSD) Part 2:standard for operating procedure of cleaning,disinfection and sterilization

实施日期：2009-12-01

NF S99-501-7-2008

Biological evaluation of medical devices - Part 7 : ethylene oxide sterilization residuals.

ISO 20857-2010

医疗保健产品灭菌 干热 医疗器械灭菌工艺的设定、确认和常规控制的要求

Sterilization of health care products. Dry heat. Requirements for the development,validation and routine control of a sterilization process for medical devices

发布日期：2010-08-17  实施日期：2010-08-15

EN ISO 10993-7-2008

Biological evaluation of medical devices. Part 7:Ethylene oxide sterilization residuals

实施日期：2008-10-01

ISO 10993-7 CORR 1-2009

Biological evaluation of medical devices. Part 7:Ethylene oxide sterilization residuals technical corrigendum 1 second edition

实施日期：2009-11-15

ISO 10993-7-2008

医疗器械的生物学评价 第7部分:环氧乙烷灭菌残留量

Biological evaluation of medical devices. Part 7:Ethylene oxide sterilization residuals second edition

发布日期：2008-10-13  实施日期：2008-10-15

ANSI/AAMI/ISO 10993-7-2008

Biological evaluation of medical devices. Part 7:Ethylene oxide sterilization residuals includes errata:January 22,2010 [:Aami tir19 amd 1,aami tir19]

实施日期：2008-01-01

BS EN ISO 10993-7-2008

Biologische Beurteilung von Medizinprodukten. Ethylenoxid-Sterilisationsrückst?nde Biological evaluation of medical devices Part 7:Ethylene oxide sterilization residuals ?valuation biologique des dispositifs médicaux. Résidus de stérilisation. l'oxyde d'éthylène CORR:July 31,2010

实施日期：2008-12-31

BS EN ISO 20857-2013

保健品灭菌 干热法 医疗器械灭菌过程的开发,验证和常规控制要求

Sterilization of health care products. Dry heat. Requirements for the development, validation and routine control of a sterilization process for medical devices

发布日期：2013-04-30  实施日期：2013-04-30

EN ISO 20857-2013

保健品消毒 干热 医疗器材消毒步骤的制定,确认和常规控制要求

Sterilization of health care products. Dry heat. Requirements for the development,validation and routine control of a sterilization process for medical devices

实施日期：2013-04-01

ANSI/AAMI/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

实施日期：2010-01-01

DIN EN ISO 10993-7-2009

医疗器械生物学评价 第7部分:环氧乙烷灭菌残留量

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals

适用范围：This part of ISO 10993 specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin(ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO and E...

实施日期：2009-02-01