发布时间：2024-05-27 17:49:26 - 更新时间：2024年06月29日 15:22
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The following National Stock Number is covered by this document:6530-01-166-9014
SANDBAG, PHYSICAL THERAPY
This commercial item description covers a dumbbell set complete with mobile storage wagon suitable for physical therapy
DUMBBELL SET, PHYSICAL THERAPY
The following National Stock Number is covered by this document
PARALLEL BARS, PHYSICAL THERAPY
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
The ?allowing National Stock Number is covered by this document
MAT, EXERCISE, PHYSICAL THERAPY
Medical devices. Biological evaluation of medical devices. Part 20. Principles and methods for immunotoxicology testing of medical devices
This commercial item description covers an exercise mat platform suitable for use in physical. therapy
PLATFORM, EXERCISE MAT, PHYSICAL THERAPY
Pyrogenicity. Principles and methods for pyrogen testing of medical devices
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
Medical devices. Application of risk management to medical devices
Medical devices—Application of risk management to medical devices
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
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
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
Medical devices - Application of risk management to medical devices
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
Medical devices. Application of risk management to medical devices
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)
Medical devices — Application of risk management to medical devices
Medical devices — Application of risk management to medical devices
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
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
Medical devices -- Application of risk management to medical devices
Medical devices.application of risk management to medical devices
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
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
Biological evaluation of medical devices－Part 20：Principles and methods for immunotoxicology testing of medical devices
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
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