Need help?

EN ISO 10079-3:2009 Standard

wave
Save  

  Keywords:

#equipment #electronic #components #controlled #electrical

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Medical suction equipment - Part 3: Suction equipment powered from a vacuum or pressure source (ISO 10079-3:1999)

  Purpose

This part of ISO 10079 specifies safety and performance requirements for medical suction equipment powered froma vacuum or pressure source (see Figure 1). In particular it applies to connections for pipelines and Venturiattachments.Suction equipment with components controlled by electrical means, e.g. electronic timing, may also need to complywith IEC 60601-1.

  Publication

Friday 17th of November 2017

  Reference

This standard supersedes the "EN ISO 10079-3:1999"

Anyway is still possible use the "EN ISO 10079-3:1999" until March 21st, 2010

  Related Standards

EN ISO 22523:2006

Medical devices Directive (93/42/EEC)

External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006)

EN 60601-2-27:2006

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-27: Particular requirements for the safety, including essential performance, of electrocardi...

EN 60601-2-33:2010/A2:2015

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic reson...

EN 60601-2-33:2010/A1:2015

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic reson...

EN 60601-2-33:2010

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic reson...

EN 60601-2-30:2000

Medical devices Directive (93/42/EEC)

Medical electrical equipment -- Part 2-30: Particular requirements for the safety, including essential performance, of automatic c...

  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 10079-3:2009 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