Need help?

EN ISO 18777:2009 Standard

wave
Save  

  Keywords:

#used #devices #care #supply #standard

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Transportable liquid oxygen systems for medical use - Particular requirements (ISO 18777:2005)

  Purpose

This International Standard specifies requirements for the safety and essential performance of transportable liquid oxygen systems which are used as a supply source for oxygen therapy. These devices usually consist of a portable unit to be carried by or with the patient whilst in use and the vessel used to refill the portable unit. These devices are mostly used in home care applications and in health care facilities/institutions. These devices are often used without professional supervision. Liquid oxygen vessels used as a supply source for oxygen pipeline systems are excluded from this International Standard.

  Publication

Friday 17th of November 2017

  Reference

This standard supersedes the "EN ISO 18777:2005"

Anyway is still possible use the "EN ISO 18777:2005" until March 21st, 2010

  Related Standards

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...

EN ISO 15002:2008

Medical devices Directive (93/42/EEC)

Flow-metering devices for connection to terminal units of medical gas pipeline systems (ISO 15002:2008)

EN 14562:2006

Medical devices Directive (93/42/EEC)

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for in...

EN 14563:2008

Medical devices Directive (93/42/EEC)

Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activi...

EN ISO 14602:2011

Medical devices Directive (93/42/EEC)

Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010)

EN ISO 14630:2009

Medical devices Directive (93/42/EEC)

Non-active surgical implants - General requirements (ISO 14630:2008)

  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 18777:2009 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