Need help?

EN 13976-2:2011 Standard

wave
Save  

  Keywords:

#standard #transportation #equipment #transport #european

This standard is superseded by:
  •   EN 13976-2:2018
  •   Directive

    Medical devices Directive (93/42/EEC)

      Last Official Journal reference

    Wednesday 14th of April 2021

      Description:

    Rescue systems - Transportation of incubators - Part 2: System requirements

      Purpose

    This European Standard specifies the requirements for a transport incubator system needed for care and treatment of infants, used in emergency or planned transport. It specifies the particular requirements needed to ensure the proper function of equipment during transportation (e.g. monitors, respirators, infusion pumps, extra corporeal lung support- (ECLS-) systems, gas supply) and to provide safe transportation for infants and operators. This European Standard also stipulates that the equipment or systems shall not interfere with the functions of the ambulance providing transportation. This European Standard does not give requirements for the vehicles, crafts, devices or incubators as such, these requirements are found in other standards. However, transport incubators are normally combined with other equipment to form a “transport incubator system”.

      Publication

    Friday 17th of November 2017

      Cessation

    This standard has been withdrawn on 2021-09-30

      Reference

    This standard supersedes the "EN 13976-2:2003"

    Anyway is still possible use the "EN 13976-2:2003" until November 30th, 2011

      Related Standards

    EN ISO 9360-2:2009

    Medical devices Directive (93/42/EEC)

    Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HME...

    EN ISO 16061:2009

    Medical devices Directive (93/42/EEC)

    Instrumentation for use in association with non-active surgical implants - General requirements (ISO 16061:2008, Corrected version...

    EN ISO 21534:2009

    Medical devices Directive (93/42/EEC)

    Non-active surgical implants - Joint replacement implants - Particular requirements (ISO 21534:2007)

    EN 20594-1:1993/AC:1996

    Medical devices Directive (93/42/EEC)

    Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (...

    EN 20594-1:1993/A1:1997

    Medical devices Directive (93/42/EEC)

    Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (...

    EN 20594-1:1993

    Medical devices Directive (93/42/EEC)

    Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (...

      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 13976-2:2011 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