Need help?

EN ISO 7396-1:2007 Standard

wave
Save  

  Keywords:

#systems #requirements #correct #gas #provision

This standard can be totally or partially supervised by:
  •   EN ISO 7396-1:2007/A1:2010
  •   EN ISO 7396-1:2007/A2:2010
  •   Directive

    Medical devices Directive (93/42/EEC)

      Last Official Journal reference

    Wednesday 14th of April 2021

      Description:

    Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007)

      Purpose

    This part of ISO 7396 specifies requirements for design, installation, function, performance, documentation, testing and commissioning of pipeline systems for compressed medical gases, gases for driving surgical tools and vacuum in healthcare facilities to ensure continuous delivery of the correct gas and the provision of vacuum from the pipeline system. It includes requirements for supply systems, pipeline distribution systems, control systems, monitoring and alarm systems and non-interchangeability between components of different gas systems.

      Publication

    Friday 17th of November 2017

      Related Standards

    EN ISO 14607:2018

    Medical devices Directive (93/42/EEC)

    Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2018, Corrected version 2018-08)

    EN 1865-3:2012

    Medical devices Directive (93/42/EEC)

    Patient handling equipment used in road ambulances - Part 3: Heavy duty stretcher

    EN 455-3:2006

    Medical devices Directive (93/42/EEC)

    Medical gloves for single use - Part 3: Requirements and testing for biological evaluation

    EN 455-4:2009

    Medical devices Directive (93/42/EEC)

    Medical gloves for single use - Part 4: Requirements and testing for shelf life determination

    EN 556-1:2001

    Medical devices Directive (93/42/EEC)

    Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminal...

    EN 556-1:2001/AC:2006

    Medical devices Directive (93/42/EEC)

    Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminal...

      Stay up to date

    CELAB is Notified Body No.2037 for the EMC Directive and Italian office of a Notified Body for the RED Directive.

    CELAB performs voluntary inspection activities on technical construction files to check their contents.

    CELAB can accomplish all the required tests in order to affix the CE-marking related to EMC, LVD, RED, MDD, machines and many others.

    CLICK HERE TO GET TESTS AND INFO ON THE EN ISO 7396-1:2007 STANDARD

      ACCESS

    Search for a standard
    GO

    Register

    Already a member?
    Login

      OTHER APPLICATIONS

    If you are interested in DO160 tests, you can give a try to our other free of charge software:
    CE-Marking assistant, Version: 1.3.0