UNE-EN 1041-2009
Information supplied by the manufacturer of medical devices
医疗器械制造商提供的信息
2009-02-18
KS P ISO 20417
의료기기 — 제조자가 제공하는 정보
医疗器械.制造商提供的信息
2022-12-28
EN ISO 20417-2021
Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12)
医疗器械制造商提供的信息
2021-05-05
ISO 20417-2021
Medical devices — Information to be supplied by the manufacturer
医疗器械制造商提供的信息
2021-04-13
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
UNE-EN 1041-1998
INFORMATION SUPPLIED BY THE MANUFACTURER WITH MEDICAL DEVICES.
由医疗器械制造商提供的信息
1998-11-13
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
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
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
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 17664-2
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
ANSI/NEMA HN 1-2019
Manufacturer Disclosure Statement for Medical Device Security
医疗器械安全制造商披露声明
AAMI/ISO TIR20416-2020
Medical devices - Post-market surveillance for manufacturers
医疗器械.制造商的上市后监督
2020-02-16
KS P ISO TR 20416
의료기기 제조자를 위한 시판 후 감시
医疗器械.制造商的上市后监督
2022-12-28
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
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
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 - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)
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
2021-09-01
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
AAMI TIR97-2019/(R)2023
Principles for medical device security - Postmarket risk management for device manufacturers
医疗器械安全原则.器械制造商的上市后风险管理
2019-09-27
KS P ISO 19001(2022 Confirm)
체외진단용 의료기기 — 생물학에서 염색을 위한 체외진단 시약에 대하여 제조자가 제공하여야 할 정보
体内诊断医疗器械.生物学染色用体外诊断试剂制造商提供的信息
2017-12-29