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

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

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

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

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

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

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

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

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

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

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

Implants for surgery. Active implantable medical devices-General requirements for safety, marking and for information to be provided by the manufacturer
外科植入物 主动植入式医疗设备

2015-06-30

Active implantable medical devices, Part 1: General requirements for safety, marking and information to be provided by the manufacturer
主动植入式医疗器械第1部分:制造商提供的安全、标志和信息的一般要求

2002-06-28

ACTIVE IMPLANTABLE MEDICAL DEVICES. PART 1: GENERAL REQUIREMENTS FOR SAFETY, MARKING AND INFORMATION TO BE PROVIDED BY THE MANUFACTURER.
主动植入式医疗设备 第1部分:制造商提供的安全、标记和信息的一般要求

1998-05-22

Implants for surgery - Active implantable medical devices, Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
外科植入物.主动植入式医疗器械.第1部分:安全、标记和制造商提供信息的一般要求

2015-07-17

외과용 이식재 — 기능성 이식형 의료기기 — 제1부: 제조회사가 제공해야 하는 안전성, 표시, 정보에 대한 기본 요구사항
手术植入物 - 有源植入式医疗器械 - 第1部分:安全 标记和供应商信息的一般要求

2018-12-21

手术植入物　有源植入式医疗器械　第1部分：安全、标记和制造商所提供信息的通用要求
Implants for surgery—Active implantable medical devices—Part 1:General requirements for safety,marking and for information to be provided by the manufacturer

2015-12-10

외과용 이식재 — 기능성 이식형 의료기기 — 제1부: 제조회사가 제공해야 하는 안전성, 표시, 정보에 대한 기본 요구사항
外科植入物.有源植入式医疗器械.第1部分:安全性、标记和制造商提供的信息的一般要求

2018-12-21

Implants for surgery - Active implantable medical devices - Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
外科植入物.主动植入式医疗器械.第1部分:制造商提供的安全、标记和信息的一般要求

2014-10-08

Implants for surgery — Active implantable medical devices — Part 1: General requirements for safety, marking and for information to be provided by the manufacturer
手术植入物 - 有源植入式医疗器械 - 第1部分:制造商提供的安全 标记和信息的一般要求

2014-08-11