Skip to content
Please enter a keyword to search

  • VDI 5700 Blatt 2:2017-06

    View superseded by
    Superseded A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
    View superseded by

    Reprocessing hazards - Risk management in reprocessing of medical devices - Trainings

    Available format(s):  Hardcopy, PDF

    Superseded date:  03-03-2023

    Language(s):  German - English

    Published date:  01-06-2017

    Publisher:  Verlag des Vereins Deutscher Ingenieure

    Add To Cart

    Table of Contents - (Show below) - (Hide below)

    Preliminary note
    Introduction
    1 Scope
    2 Normative references
    3 Terms and definitions
    4 Abbreviations
    5 Training categories and training
       prerequisites
    6 Qualification of experts
    7 Quality characteristics of training
       courses and instructions
    8 Training subjects and contents
    9 Examinations
    10 Certificates
    Annex A - Training subjects and contents
    Annex B - Certificate template
    Bibliography

    Abstract - (Show below) - (Hide below)

    Applies to courses for further training of staff in the field of reprocessing of medical devices (process-related training) and of staff of medical devices manufacturers, particularly developers (device-related training).

    General Product Information - (Show below) - (Hide below)

    Document Type Standard
    Publisher Verlag des Vereins Deutscher Ingenieure
    Status Superseded
    Superseded By
    Supersedes

    Standards Referencing This Book - (Show below) - (Hide below)

    DIN EN ISO 17664:2016-06 (Draft) PROCESSING OF HEALTH CARE PRODUCTS - INFORMATION TO BE PROVIDED BY THE MEDICAL DEVICE MANUFACTURER FOR THE PROCESSING OF MEDICAL DEVICES (ISO 17664:2017)
    DIN EN ISO 14971:2013-04 MEDICAL DEVICES - APPLICATION OF RISK MANAGEMENT TO MEDICAL DEVICES (ISO 14971:2007)
    VDI 5700 Blatt 1:2015-04 Reprocessing hazards - Risk management in reprocessing of medical devices - Measures for risk control
    VDI 1000:2017-02 VDI Standardisation Work - Principles and procedures
    ISO 10993-1:2009 Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
    EN ISO 10993-1:2009/AC:2010 BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)
    View more information

    • Access your standards online with a subscription

      Features

      • Simple online access to standards, technical information and regulations
      • Critical updates of standards and customisable alerts and notifications
      • Multi - user online standards collection: secure, flexibile and cost effective