Need help?

EN 1820:2005/A1:2009 Standard

wave
Save  

  Keywords:

#anaesthetic #systems #use #requirements #antistatic

  Directive

Medical devices Directive (93/42/EEC)

  Description:

Anaesthetic reservoir bags (ISO 5362:2000, modified)

  Purpose

This European Standard specifies requirements for antistatic and non-antistatic reservoir bags for use with anaesthetic apparatus or lung-ventilator breathing systems. It includes requirements for the design of the neck, size designation, distension and, where relevant, for electrical resistance. This document is not applicable to special-purpose bags, for example bellows and self-expanding bags. Bags for use with anaesthetic gas scavenging systems are not considered to be anaesthetic reservoir bags and are thus outside the scope of this document.

  Publication

Friday 17th of November 2017

  Amendment

This standard is an amendment for "EN 1820:2005"

  Reference

This standard supersedes the "EN 1820:2005"

Anyway is still possible use the "EN 1820:2005" until March 21st, 2010

  Related Standards

EN 60601-2-1:1998

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 ...

EN 60601-2-44:2009

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipmen...

EN 60601-2-36:1997

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotrips...

EN 60601-2-37:2008

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic med...

EN 60601-2-39:2008

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysi...

EN 60601-2-40:1998

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment...

  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 1820:2005/A1:2009 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