共找到 150 条与 EN ISO 14971 相关的标准,共 10

Medical devices - Application of risk management to medical devices (ISO 14971:2007); German version EN ISO 14971:2007, Corrigenda to DIN EN ISO 14971:2007-07

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, Corrected version 2007-10-01); English version of DIN EN ISO 14971:2009-10

Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01); German version EN ISO 14971:2012

Medical devices - Application of risk management to medical devices (ISO 14971:2019)

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

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. (ISO 14971:2000)

  Full Description ADOPTED_FROM:EN ISO 14971:2019 This document specifies terminology, principles and a process for risk

Medical devices — Application of risk management to medical devices (ISO 14971:2019)

  Full Description This standard is identical to ISO 14971:2007

Medical devices - Application of risk management to medical devices (ISO 14971:2007)

  Full Description ADOPTED_FROM:EN ISO 14971:2007 This International Standard specifies a process for a manufacturer to identify

Medical devices - Application of risk management to medical devices (ISO 14971:2007)

BS EN ISO 14971. Medical devices. Application of risk management to medical devices

Draft Document - Medical devices - Application of risk management to medical devices (ISO/DIS 14971:2018); German and English version prEN ISO 14971:2018

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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