医疗器械（无菌）检测

EN 13824:2004 医疗器械灭菌 液体医疗器械的菌处理 要求

Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements

EN 556:1994 医疗器械灭菌 医疗器械贴有“菌”标签的要求

Sterilization of Medical Devices - Requirements for Medical Devices to Be Labelled `Sterile'

ASTM F1980-07(2011 医疗器械菌阻隔系统加速老化的标准指南

The loss of sterile barrier system integrity may occur as a result of physical properties of the materials and adhesive or cohesive bonds degrading

Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices

prEN 556-1991 医疗器械的杀菌.标有"Sterile"的医疗器械的菌保证等级.要求

Sterilization of medical devices; sterility assurance level for medical devices labelled "Sterile"; requirements

UNE-EN 556-2:2016 医疗器械灭菌 指定为“菌”医疗器械的要求 第2部分：菌处理医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices

LST EN 556-2-2004 医疗器械灭菌 指定为“菌”的医疗器械的要求 第2部分：菌处理医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices

YY/T 0615.2-2007 标示“菌”医疗器械的要求 第2部分：菌加工医疗器械的要求

YY/T 0615的本部分规定了标示“菌”的菌加工医疗器械的要求。 注：医疗器械只有当使用了一个确认过的灭菌过程，才可以标示“菌”。YY/T 0567规定了菌加工的确认和常规控制

Requirements for medical devices to be dwsignated“SIERILE”.Part 2:Requirements for aseptically processed medical devices

NF S98-107-2*NF EN 556-2:2015 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第2部分：菌处理医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2 : requirements for aseptically processed medical devices

DS/EN 556-2:2004 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第2部分：菌处理医疗器械的要求

This standard specifies the requirements for an aseptically processed medical device to be designated ""STERILE

Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 2: Requirements for aseptically processed medical devices

23/30457240 DC BS EN 556-2 医疗器械的灭菌 标记为“菌”的医疗器械的要求 第 2 部分：菌加工医疗器械的要求

BS EN 556-2. Sterilization of medical devices. Requirements for medical devices to be designated ''STERILE" - Part 2. requirements for aseptically processed medical devices

BS EN 556-2:2015 跟踪更改 医疗器械的灭菌 医疗器械被指定为“菌”的要求 菌加工医疗器械的要求

Tracked Changes. Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE'. Requirements for aseptically processed medical devices

EN 556:1998 医疗器械灭菌 最终要求 灭菌医疗器械贴上“菌”标签批准的欧洲文本；包括修正案 1：1994

Sterilization of Medical Devices - Requirements for Terminally - Sterilized Medical Devices to Be Labelled "Sterile" Ratified European Text; Includes Amendment 1: 1994

UNE-EN 556-1:2002/AC:2007 医疗器械灭菌 指定为“菌”医疗器械的要求 第1部分：最终灭菌医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices

DS/EN 556-1/AC:2006 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第1部分：最终灭菌医疗器械的要求

Corrigendum to EN 556-1:2001:This standard specifies the requirements for a terminally-sterilized medical device to be designated ""STERILE

Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 1: Requirements for terminally sterilized medical devices

DS/EN 556-1:2002 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第1部分：最终灭菌医疗器械的要求

This standard specifies the requirements for a terminally-sterilized medical device to be designated ""STERILE

Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 1: Requirements for terminally sterilized medical devices

EN 13824:2004 医疗器械灭菌 液体医疗器械的菌处理 要求

Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements

EN 556:1994 医疗器械灭菌 医疗器械贴有“菌”标签的要求

Sterilization of Medical Devices - Requirements for Medical Devices to Be Labelled `Sterile'

ASTM F1980-07(2011 医疗器械菌阻隔系统加速老化的标准指南

The loss of sterile barrier system integrity may occur as a result of physical properties of the materials and adhesive or cohesive bonds degrading

Standard Guide for Accelerated Aging of Sterile Barrier Systems for Medical Devices

prEN 556-1991 医疗器械的杀菌.标有"Sterile"的医疗器械的菌保证等级.要求

Sterilization of medical devices; sterility assurance level for medical devices labelled "Sterile"; requirements

UNE-EN 556-2:2016 医疗器械灭菌 指定为“菌”医疗器械的要求 第2部分：菌处理医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE" - Part 2: Requirements for aseptically processed medical devices

LST EN 556-2-2004 医疗器械灭菌 指定为“菌”的医疗器械的要求 第2部分：菌处理医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices

YY/T 0615.2-2007 标示“菌”医疗器械的要求 第2部分：菌加工医疗器械的要求

YY/T 0615的本部分规定了标示“菌”的菌加工医疗器械的要求。 注：医疗器械只有当使用了一个确认过的灭菌过程，才可以标示“菌”。YY/T 0567规定了菌加工的确认和常规控制

Requirements for medical devices to be dwsignated“SIERILE”.Part 2:Requirements for aseptically processed medical devices

NF S98-107-2*NF EN 556-2:2015 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第2部分：菌处理医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated ''STERILE'' - Part 2 : requirements for aseptically processed medical devices

DS/EN 556-2:2004 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第2部分：菌处理医疗器械的要求

This standard specifies the requirements for an aseptically processed medical device to be designated ""STERILE

Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 2: Requirements for aseptically processed medical devices

23/30457240 DC BS EN 556-2 医疗器械的灭菌 标记为“菌”的医疗器械的要求 第 2 部分：菌加工医疗器械的要求

BS EN 556-2. Sterilization of medical devices. Requirements for medical devices to be designated ''STERILE" - Part 2. requirements for aseptically processed medical devices

BS EN 556-2:2015 跟踪更改 医疗器械的灭菌 医疗器械被指定为“菌”的要求 菌加工医疗器械的要求

Tracked Changes. Sterilization of medical devices. Requirements for medical devices to be designated 'STERILE'. Requirements for aseptically processed medical devices

EN 556:1998 医疗器械灭菌 最终要求 灭菌医疗器械贴上“菌”标签批准的欧洲文本；包括修正案 1：1994

Sterilization of Medical Devices - Requirements for Terminally - Sterilized Medical Devices to Be Labelled "Sterile" Ratified European Text; Includes Amendment 1: 1994

UNE-EN 556-1:2002/AC:2007 医疗器械灭菌 指定为“菌”医疗器械的要求 第1部分：最终灭菌医疗器械的要求

Sterilization of medical devices - Requirements for medical devices to be designated 'STERILE' - Part 1: Requirements for terminally sterilized medical devices

DS/EN 556-1/AC:2006 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第1部分：最终灭菌医疗器械的要求

Corrigendum to EN 556-1:2001:This standard specifies the requirements for a terminally-sterilized medical device to be designated ""STERILE

Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 1: Requirements for terminally sterilized medical devices

DS/EN 556-1:2002 医疗器械灭菌 被指定为“菌”的医疗器械的要求 第1部分：最终灭菌医疗器械的要求

This standard specifies the requirements for a terminally-sterilized medical device to be designated ""STERILE

Sterilization of medical devices - Requirements for medical devices to be designated ""STERILE"" - Part 1: Requirements for terminally sterilized medical devices