BS EN ISO 14971:2007 医疗设备.医疗设备风险管理的应用
ISO 14971:2007 specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD
Medical devices - Application of risk management to medical devices
DIN EN 62366:2008 医疗设备.医疗设备可用性工程的应用
Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
BS EN 62366:2008 医疗设备.医疗设备可用性工程的应用
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates
Medical devices - Application of usability engineering to medical devices
NF C74-054:2008 医疗设备.医疗设备可用性工程的应用
Medical devices - Application of usability engineering to medical devices.
ANSI/AAMI/IEC 62366:2007 医疗设备.医疗设备易用性工程应用件
This standard describes a usability engineering process, and provides guidance on how to implement and execute the process to provide safety
Medical devices - Application of usability engineering to medical devices
DIN EN ISO 14971:2007 医疗设备.医疗设备风险管理的应用(ISO 14971-2007)
This International Standard specifies a process for a manufacturer to identify the hazards associated with medical devices,including in vitro
Medical devices - Application of risk management to medical devices (ISO 14971:2007); German version EN ISO 14971:2007
ISO 15225:2010 医疗设备.质量管理.医疗设备命名法数据结构
Medical devices - Quality management - Medical device nomenclature data structure
ISO 15225:2016 医疗设备.质量管理.医疗设备命名法数据结构
Medical devices - Quality management - Medical device nomenclature data structure
BS EN 13824:2004 医疗设备的灭菌.液体医疗设备的菌操作.要求
This document specifies requirements for the design and operation of aseptic processing facilities and the validation and routine control of aseptic
Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
SNI 16-4940.1-1998 电力医疗设备
Electrically powered medical suction equipment
UL 416-1993 制冷医疗设备
These requirements cover refrigerated medical equipment such as thermia and oxygen therapy devices for use in hospitals, nursing homes, medical care
UL Standard for Safety Refrigerated Medical Equipment (Fourth Edition; Reprint with Revisions Through and Including May 14@ 2004)
STAS 5316-1967 医疗设备．耳镜
SAE J3020-2014 医疗设备喷丸
This SAE Standard and its supplementary detail specifications cover the engineering requirements for the controlled shot peening of a medical device
Medical Device Shot Peening
NP EN 556-2000 医疗设备的杀菌．菌处理的医疗设备的要求
1 Esta Norma Europeia especifica os requisitos para que um dispositivo médico submetido a uma esteriliza??o final possa ser rotulado "EST?RIL". NOTA
Sterilization of medical devices Requirements for terminally sterilized medical devices to be labelled"Sterile"
ISO/TR 15223:1998 医疗设备.医疗设备标签、加标签和所提供的信息用符号
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied
BS EN ISO 14971:2007 医疗设备.医疗设备风险管理的应用
ISO 14971:2007 specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD
Medical devices - Application of risk management to medical devices
DIN EN 62366:2008 医疗设备.医疗设备可用性工程的应用
Medical devices - Application of usability engineering to medical devices (IEC 62366:2007); German version EN 62366:2008
BS EN 62366:2008 医疗设备.医疗设备可用性工程的应用
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates
Medical devices - Application of usability engineering to medical devices
NF C74-054:2008 医疗设备.医疗设备可用性工程的应用
Medical devices - Application of usability engineering to medical devices.
ANSI/AAMI/IEC 62366:2007 医疗设备.医疗设备易用性工程应用件
This standard describes a usability engineering process, and provides guidance on how to implement and execute the process to provide safety
Medical devices - Application of usability engineering to medical devices
DIN EN ISO 14971:2007 医疗设备.医疗设备风险管理的应用(ISO 14971-2007)
This International Standard specifies a process for a manufacturer to identify the hazards associated with medical devices,including in vitro
Medical devices - Application of risk management to medical devices (ISO 14971:2007); German version EN ISO 14971:2007
ISO 15225:2010 医疗设备.质量管理.医疗设备命名法数据结构
Medical devices - Quality management - Medical device nomenclature data structure
ISO 15225:2016 医疗设备.质量管理.医疗设备命名法数据结构
Medical devices - Quality management - Medical device nomenclature data structure
BS EN 13824:2004 医疗设备的灭菌.液体医疗设备的菌操作.要求
This document specifies requirements for the design and operation of aseptic processing facilities and the validation and routine control of aseptic
Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
SNI 16-4940.1-1998 电力医疗设备
Electrically powered medical suction equipment
UL 416-1993 制冷医疗设备
These requirements cover refrigerated medical equipment such as thermia and oxygen therapy devices for use in hospitals, nursing homes, medical care
UL Standard for Safety Refrigerated Medical Equipment (Fourth Edition; Reprint with Revisions Through and Including May 14@ 2004)
STAS 5316-1967 医疗设备．耳镜
SAE J3020-2014 医疗设备喷丸
This SAE Standard and its supplementary detail specifications cover the engineering requirements for the controlled shot peening of a medical device
Medical Device Shot Peening
NP EN 556-2000 医疗设备的杀菌．菌处理的医疗设备的要求
1 Esta Norma Europeia especifica os requisitos para que um dispositivo médico submetido a uma esteriliza??o final possa ser rotulado "EST?RIL". NOTA
Sterilization of medical devices Requirements for terminally sterilized medical devices to be labelled"Sterile"
ISO/TR 15223:1998 医疗设备.医疗设备标签、加标签和所提供的信息用符号
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied
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