现行

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

现行

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

现行

YY/T 1478-2016

可重复使用医疗器械消毒灭菌的追溯信息
Traceability information of disinfection and sterilization reusable medical devices

2016-07-29

现行

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

现行

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

现行

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

现行

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

现行

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

现行

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

现行

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

现行

BS EN 45502-1-2015

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

现行

AS EN 45502.1-2002

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

现行

UNE-EN 45502-1-1998

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

现行

AS ISO 14708.1-2015

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

现行

KS P ISO 14708-1

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

现行

GB 16174.1-2015

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

现行

KS P ISO 14708-1(2023 Confirm)

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

现行

AAMI/ISO 14708-1-2014

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

现行

ISO 14708-1-2014

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

现行

GOST R ISO 14708-1-2012

Имплантаты хирургические. Активные имплантируемые медицинские изделия. Часть 1. Общие требования к безопасности, маркировке и информации, предоставляемой изготовителем
手术植入物 主动植入式医疗器械 第一部分制造商提供的安全 标识和信息的一般要求