Need help?

EN 13976-1:2011 Standard

wave
Save  

  Keywords:

#requirements #equipment #care #incubator #european

  Directive

Medical devices Directive (93/42/EEC)

  Last Official Journal reference

Wednesday 14th of April 2021

  Description:

Rescue systems - Transportation of incubators - Part 1: Interface conditions

  Purpose

This European Standard specifies the requirements for the interface between the ambulance and the incubator and the associated equipment, needed for care and treatment of infants, used in emergency or planned transports to ensure interchangeability and interoperability and to provide uninterrupted care of patients. This European Standard does not give requirements for the vehicles, crafts, devices or incubators as such; these requirements are found in other standards. However, transport incubators are normally combined with other equipment to form a "transport incubator system".

  Publication

Friday 17th of November 2017

  Reference

This standard supersedes the "EN 13976-1:2003"

Anyway is still possible use the "EN 13976-1:2003" until November 30th, 2011

  Related Standards

EN 62220-1:2004

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum e...

EN 60601-2-20:2009

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transpo...

EN 60601-2-8:1997/A1:1997

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 60601-2-10:2000

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulatorsIEC 60601-2-10:198...

EN 60601-2-10:2000/A1:2001

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulatorsIEC 60601-2-10:198...

EN 60601-2-11:1997

Medical devices Directive (93/42/EEC)

Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipmentIEC 60601-2-11:199...

  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 13976-1:2011 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