非无菌医疗器械产品检测

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

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'

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

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

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

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

DS/ISO/TS 22421:2021 医疗保健产品灭菌—医疗保健场所医疗器械终端灭菌灭菌器通用要求

Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities

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

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

YY/T 0567.7-2016 医疗保健产品的菌加工 第7部分：医疗器械及组合型产品的替代加工

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

NF EN ISO 13408-7:2015 医疗保健产品的菌加工 - 第 7 部分：医疗器械和组合产品的替代工艺

Traitement aseptique des produits de santé - Partie 7 : procédés alternatifs pour les dispositifs médicaux et les produits de combinaison

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

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

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'

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

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

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

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

DS/ISO/TS 22421:2021 医疗保健产品灭菌—医疗保健场所医疗器械终端灭菌灭菌器通用要求

Sterilization of health care products – Common requirements for sterilizers for terminal sterilization of medical devices in health care facilities

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

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

YY/T 0567.7-2016 医疗保健产品的菌加工 第7部分：医疗器械及组合型产品的替代加工

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

NF EN ISO 13408-7:2015 医疗保健产品的菌加工 - 第 7 部分：医疗器械和组合产品的替代工艺

Traitement aseptique des produits de santé - Partie 7 : procédés alternatifs pour les dispositifs médicaux et les produits de combinaison

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