Need help?

EN ISO 11990-1:2014 Standard

wave
Save  

  Keywords:

#fire #used #laser #describe #can

This standard is superseded by:
  •   EN ISO 11990:2018
  •   Directive

    Medical devices Directive (93/42/EEC)

      Last Official Journal reference

    Wednesday 14th of April 2021

      Description:

    Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 1: Tracheal tube shaft (ISO 11990-1:2011)

      Purpose

    ISO 11990-1:2011 specifies a method of testing the continuous wave (cw) resistance of the shaft of a tracheal tube designed to resist ignition by a laser. It is not applicable to other components of the system, such as the inflation system and cuff, which are defined in ISO 11990-2:2010. ISO 11990-1:2011 can be used to measure and describe the properties of materials, products or assemblies in response to heat and flame under controlled laboratory conditions. It does not describe or appraise the fire hazard or fire risk of materials, products, or assemblies under actual clinical use conditions. However, the results of this test can be used as one element of a fire risk assessment which takes into account all factors pertinent to an assessment of the hazard of a particular end use.

      Publication

    Friday 17th of November 2017

      Cessation

    This standard will be withdrawn on 2021-09-30

      Related Standards

    EN 60601-1-1:2001

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical el...

    EN 27740:1992/A1:1997

    Medical devices Directive (93/42/EEC)

    Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)

    EN 60601-2-8:1997

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the rang...

    EN 60601-2-5:2000

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 2-5: Particular requirements for the safety of ultrasonic physiotherapy equipmentIEC 60601-2-5...

    EN 60601-2-3:1993

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 2: Particular requirements for the safety of short-wave therapy equipmentIEC 60601-2-3:1991

    EN 60601-2-1:1998/A1:2002 (IEC 60601-2-1:1998/A1:2002)

    Medical devices Directive (93/42/EEC)

    Medical electrical equipment - Part 2-1: Particular requirements for the safety of electron accelerators in the range of 1 MeV to ...

      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 11990-1:2014 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