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EN ISO 14971:2019 Standard

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  Keywords:

#eu #relationship #a11 #found #can

This standard can be totally or partially supervised by:
  •   EN ISO 14971:2019/A11:2021
  •   Directive

    In vitro diagnostic medical devices Regulation ((EU) 2017/746)

      Last Official Journal reference

    Wednesday 28th of January 2026

      Description:

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

      Purpose

    ISO 14971 specifies terminology, principles and a process for risk management of medical devices, including software as a medical device and in vitro diagnostic medical devices. The main text and the consolidated version which consists of main text and the amendment can be found in the standard’s history. EN ISO 14971:2019/A11:2021 modifies the European standard EN ISO 14971:2019. EN ISO 14971:2019/A11:2021 supports the requirements of EU Regulations.The relationship with EU Regulations can be found in informative annexes: — Annex ZA covers the relationship between EN ISO 14971 and the General Safety and Performance Requirements of Regulation (EU) 2017/745. — Annex ZB covers the relationship between EN ISO 14971 and the General Safety and Performance Requirements of Regulation (EU) 2017/746.

      Publication

    Thursday 12th of May 2022

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