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EN 12342:1998/A1:2009 Standard

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  Keywords:

#breathing #standard #ends #assembled #requirements

  Directive

Medical devices Directive (93/42/EEC)

  Description:

Breathing tubes intended for use with anaesthetic apparatus and ventilators

  Purpose

This European Standard specifies the basic requirements for breathing tubes and breathing tubing supplied to be cut to length, intended for use with anaesthetic apparatus and ventilators, humidifiers and nebulizers. It also applies to breathing tubes and Y-pieces supplied already assembled and to those supplied as components and assembled in accordance with the manufacturers' instructions. Provision is made for breathing tubes having ends incorporating adaptors with conical connectors (assembled ends) or with plain ends (either cylindrical or tapered). Breathing tubes for special purposes, such as those used with ventilators having special compliance requirements and coaxial lumen tubes, are outside the scope of this European Standard. Unless specified otherwise, the requirements of this European Standard apply equally to breathing tubes intended by the manufacturer for single use and those intended for re-use.

  Publication

Friday 17th of November 2017

  Amendment

This standard is an amendment for "EN 12342:1998"

  Reference

This standard supersedes the "EN 12342:1998"

Anyway is still possible use the "EN 12342:1998" until March 21st, 2010

  Related Standards

EN ISO 5366-1:2009

Medical devices Directive (93/42/EEC)

Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000)

EN 13976-2:2011

Medical devices Directive (93/42/EEC)

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

EN ISO 13408-4:2011

Medical devices Directive (93/42/EEC)

Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)

EN ISO 13408-5:2011

Medical devices Directive (93/42/EEC)

Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)

EN ISO 13408-6:2011

Medical devices Directive (93/42/EEC)

Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)

EN ISO 13408-7:2015

Medical devices Directive (93/42/EEC)

Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408...

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