YY/T 0802-2020
医疗器械的处理 医疗器械制造商提供的信息
Processing of medical devices—Information to be provided by the medical device manufacturer
2020-06-30
GOST R ISO 17664-2012
Стерилизация медицинских изделий. Информация, предоставляемая изготовителем для проведения повторной стерилизации медицинских изделий
医疗器械灭菌由制造商提供的用于处理可再次消毒的医疗设备的信息
BS ISO 17664-2-2021
Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices-Non-critical medical devices
医疗保健产品的加工 医疗器械制造商为医疗器械加工提供的信息
2021-02-26
BS EN ISO 17664-1-2021
Processing of health care products. Information to be provided by the medical device manufacturer for the processing of medical devices-Critical and semi-critical medical devices
医疗保健产品的加工 医疗器械制造商为医疗器械加工提供的信息
2021-09-01
KS P ISO 17664-2
의료 제품 공정 의료기기 제조자가 제공하는 정보 제제2부부: 비위험 의료기기
医疗保健产品加工.医疗器械制造商为医疗器械加工提供的信息.第2部分:非关键医疗器械
2022-12-28
ISO 17664-2-2021
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 2: Non-critical medical devices
医疗保健品加工医疗器械生产企业提供的医疗器械加工信息第2部分:非关键医疗器械
2021-02-25
UNE-EN ISO 17664-2004
Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)
医疗器械的灭菌.制造商为可再灭菌医疗器械的处理提供的信息（ISO 17664-2004）
2004-09-30
KS P ISO 17664-1
의료제품 공정 — 의료기기 제조자가 제공하는 정보 — 제1부: 위험 및 준위험 의료기기
医疗保健产品的加工.医疗器械制造商为医疗器械加工提供的信息.第1部分:关键和半关键医疗器械
2021-12-28
ISO 17664-1-2021
Processing of health care products — Information to be provided by the medical device manufacturer for the processing of medical devices — Part 1: Critical and semi-critical medical devices
医疗保健产品的加工医疗器械制造商为医疗器械加工提供的信息第1部分:关键和半关键医疗器械
2021-07-06
DIN EN ISO 17664
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)
医疗保健产品的加工.医疗器械制造商为医疗器械加工提供的信息（ISO 17664-2017）
2018-04-01
BS EN 556-2-2015
Sterilization of medical devices. Requirements for medical devices to be designated "STERILE"-Requirements for aseptically processed medical devices
医疗器械的消毒 指定为“无菌”医疗器械的要求
2015-09-30
UNE-EN 13824-2005
Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
医疗器械的灭菌.液体医疗器械的无菌处理.要求
2005-05-25
DIN EN 13824
Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
医疗器械的灭菌.液体医疗器械的无菌处理.要求；德文版EN 13824:2004
2005-02-01
UNE-EN 556-2-2004
Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 2: Requirements for aseptically processed medical devices
医疗器械的灭菌.指定无菌医疗器械的要求.第2部分:无菌处理医疗器械的要求
2004-06-25
DIN EN ISO 17664-1-DRAFT
Draft Document - Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO/FDIS 17664-1:2020); German and English version prEN ISO 17664-1:2021
文件草案——医疗保健产品的处理——医疗器械制造商为医疗器械的处理提供的信息——第1部分:关键和半关键医疗器械（ISO/FDIS 17664-1:2020）；德文和英文版本prEN ISO 17664-1:2021
2021-02-01
BS PD IEC/TR 80002-3-2014
Medical device software-Process reference model of medical device software life cycle processes (IEC 62304)
医疗器械软件
2014-06-04
AAMI/IEC TIR80002-3-2016
Technical Information Report Medical device software - Part 3: Process reference model of medical device software life cycle processes (IEC 62304)
医疗器械软件技术信息报告第3部分:医疗器械软件生命周期过程的过程参考模型（IEC 62304）
2016-08-12
YY/T 0615.2-2007
标示“无菌”医疗器械的要求 第2部分:无菌加工医疗器械的要求
Requirements for medical devices to be designated "STERILE"—Part 2:Requirements for aseptically processed medical devices
2007-07-02
AAMI TIR55-2014/(R)2017
Human factors engineering for processing medical devices
医疗器械加工中的人因工程
2014-12-23
CAN/CSA Z314.4-87
Industrial Sterilization of Medical Devices by the Steam Process
医疗器械的蒸汽灭菌
1987-01-01