DOD A-A-51479-1986 物理治疗法沙袋
The following National Stock Number is covered by this document:6530-01-166-9014
SANDBAG, PHYSICAL THERAPY
DOD A-A-51517-1986 物理治疗法设备
This commercial item description covers a dumbbell set complete with mobile storage wagon suitable for physical therapy
DUMBBELL SET, PHYSICAL THERAPY
DOD A-A-51622-1986 物理治疗法双杠
The following National Stock Number is covered by this document
PARALLEL BARS, PHYSICAL THERAPY
SN/T 1430.1-2004 进口医疗器械检验规程 医用超声诊断和治疗设备
本标准规定了进口医用超声诊断和治疗设备的抽样、检验及检验结果的判定。 本标准适用于进口医用超声诊断和治疗设备的检验
Rules for the inspection of medical electrical equipment for import--Ultrasonic medical diagnostic and therapy equipment
DOD A-A-51518-1986 物理治疗法锻炼垫
The ?allowing National Stock Number is covered by this document
MAT, EXERCISE, PHYSICAL THERAPY
GOST ISO/TS 10993-20-2011 医疗器械.医疗器械的生物学评价.第20部分.医疗器械的免疫毒理学测试用原理和方法
Medical devices. Biological evaluation of medical devices. Part 20. Principles and methods for immunotoxicology testing of medical devices
WS 667-2019 机械臂放射治疗装置质量控制检测规范
DOD A-A-51896-1987 物理治疗法练习垫台
This commercial item description covers an exercise mat platform suitable for use in physical. therapy
PLATFORM, EXERCISE MAT, PHYSICAL THERAPY
BS PD ISO/TR 21582:2021 致温性 医疗器械热原检测原理和方法
Pyrogenicity. Principles and methods for pyrogen testing of medical devices
DOD A-A-54719-1992 吸入治疗器械喷雾器多种组装
This Commercial Item Description covers a disposable, single use,manifold assembly with nebulizer to deliver aerosol therapy for use
NEBULIZER-MANIFOLD ASSEMBLY, INHALATION THERAPY APPARATUS
GOST ISO 14971-2011 医疗器械.医疗器械风险管理应用
Medical devices. Application of risk management to medical devices
GB/T 42062-2022 医疗器械 风险管理对医疗器械的应用
Medical devices—Application of risk management to medical devices
YY/T 0316-2008 医疗器械.风险管理对医疗器械的应用
本标准为制造商规定了一个过程，以判定与医疗器械，包括体外诊断（IVD）医疗器械有关的危害，估计和评价相关的风险，控制这些风险，并监视控制的有效性。 本标准的要求适用于医疗器械生命周期的所有阶段。 本标准不用于临床决策。 本标准不规定可接受的风险水平。 本标准不要求制造商有一个适当的质量体系
Medical devices.Application of risk management to medical devices
YY/T 0316-2016 医疗器械 风险管理对医疗器械的应用
本标准为制造商规定了一个过程，以识别与医疗器械[包括体外诊断(IVD)医疗器械]有关的危险(源)，估计和评价相关的风险，控制这些风险，并监视控制的有效性。本标准的要求适用于医疗器械生命周期的所有阶段。本标准不用于临床决策。本标准不规定可接受的风险水平。本标准不要求制造商有一个适当的质量体系。然而
Medical devices.Application of risk management to medical devices
EN ISO 14971:2019 医疗器械.医疗器械风险管理的应用
This International Standard specifies a procedure by which a manufacturer can identify the hazards associated with medical devices
Medical devices - Application of risk management to medical devices
NF S99-211:2013 医疗器械.医疗器械风险管理的应用
Medical devices - Application of risk management to medical devices
BS EN ISO 14971:2009 医疗器械.医疗器械风险管理的应用
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
BS EN ISO 14971:2012 医疗器械.医疗器械风险管理的应用
Medical devices. Application of risk management to medical devices
EN ISO 14971:2012 医疗器械.医疗器械风险管理的应用
This International Standard specifies a process for a manufacturer to identify the hazards associated withmedical devices, including in vitro
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)
KS P ISO 14971:2018 医疗器械 - 医疗器械风险管理的应用
Medical devices — Application of risk management to medical devices
KS P ISO 14971:2021 医疗器械.医疗器械风险管理的应用
Medical devices — Application of risk management to medical devices
SANS 14971:2008 医疗器械．医疗器械风险管理的应用
Specifies a process for a manufacturer to identify the hazards associated with medical devices, including in vitro diagnostic (IVD) medical devices
Medical devices - Application of risk management to medical devices
JIS T 14971:2003 医疗器械.医疗器械风险管理的应用
この規格は，製造業者がインビトロ診断機器を合む医療機器及びその附属品に関連するハザードを特定し，リスクの推定と評価を行い，これらのリスクをコントロールし，そのコントロールの有効性を監視する手順について規定する
Medical devices -- Application of risk management to medical devices
JIS T 14971:2012 医疗器械.医疗器械风险管理的应用
Medical devices -- Application of risk management to medical devices
TIS 14971-2013 医疗器械.风险管理对医疗器械的应用
Medical devices.application of risk management to medical devices
YY/T 0316-2003 医疗器械.风险管理对医疗器械的应用
本标准规定了一个程序，制造商按此程序，能够判定与医疗器械及其附件(包括体外诊断医疗器械)有关的危害，估计和评价风险，控制这些风险，并监控控制的有效性。 本标准的要求适用于医疗器械寿命周期的所有阶段。 本标准不用于和医疗器械使用有关的临床判断。 它不规定可接受的风险水平
Medical devices-Application of risk management to medical devices
ISO 14971:2000 医疗器械 对医疗器械风险管理的应用
This International Standard specifies a procedure by which a manufacturer can identify the hazards associated with medical devices
Medical devices - Application of risk management to medical devices
KS P ISO 10993-20-2009(2019 医疗器械生物学评价第20部分:医疗器械免疫毒理学试验原理和方法
Biological evaluation of medical devices－Part 20：Principles and methods for immunotoxicology testing of medical devices
WS/T 654-2019 医疗器械安全管理
BS EN ISO 14971:2001 医疗器械.风险管理在医疗器械上的应用
This International Standard specifies a procedure by which a manufacturer can identify the hazards associated with medical devices
Medical devices - Application of risk management to medical devices
编辑：北检院编辑部
