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 ISO 10993-12:2012

Medical devices Directive (93/42/EEC)

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)

EN ISO 10524-1:2006

Medical devices Directive (93/42/EEC)

Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (I...

EN ISO 9360-1:2009

Medical devices Directive (93/42/EEC)

Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HME...

EN ISO 9360-2:2009

Medical devices Directive (93/42/EEC)

Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HME...

EN ISO 9713:2009

Medical devices Directive (93/42/EEC)

Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2002)

EN ISO 10079-1:2009

Medical devices Directive (93/42/EEC)

Medical suction equipment - Part 1: Electrically powered suction equipment - Safety requirements (ISO 10079-1:1999)

  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